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		    <title>PatentStorm -&gt; Patents -&gt; Chemistry</title>
		    <link>http://www.patentstorm.us/rss/subject/patents/rss-3.xml</link>
		    <description>Recent patents filings about Chemistry.</description>
		    <pubDate>Tue, 14 May 2013 17:00:03</pubDate>
		    <managingEditor>patents@patentstorm.us</managingEditor>
		    <language>en</language><atom10:link xmlns:atom10="http://www.w3.org/2005/Atom" rel="self" type="application/rss+xml" href="http://feeds.feedburner.com/Patentstorm-Patents-Chemistry" /><feedburner:info uri="patentstorm-patents-chemistry" /><atom10:link xmlns:atom10="http://www.w3.org/2005/Atom" rel="hub" href="http://pubsubhubbub.appspot.com/" /><item>
			         <title><![CDATA[Oxidation process for the production of carboxylic acids and alkenes]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/skKQnAxMA9c/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;RE44206&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-07&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;An oxidation process for the production of alkenes and carboxylic acids from a feed comprising alkene and/or alkane, carbon monoxide, a molecular oxygen containing gas and optionally water in the presence of an oxidation catalyst in which the level of carbon monoxide is maintained between 1% and 20% by volume of the total feed to the ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/skKQnAxMA9c" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">RE44206</guid>			
			      <feedburner:origLink>http://www.patentstorm.us/patents/RE44206/description.html</feedburner:origLink></item>
<item>
			         <title><![CDATA[Process for preparing 4-aminodiphenylamines]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/si9gVVWJYs8/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;RE44175&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-04-23&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; ; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;A process for preparing an optionally substituted 4-aminodiphenylamine comprising reacting an optionally substituted aniline and an optionally substituted nitrobenzene in the presence of water and a base while controlling the water content so as to ensure a molar ratio of water to the base charged of not less than about 4:1 at the start of the coupling reaction and not less than about 0.6:1 at the end of the coupling reaction to produce 4-nitrodiphenylamine and/or 4-nitrosodiphenylamine ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/si9gVVWJYs8" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">RE44175</guid>			
			      <feedburner:origLink>http://www.patentstorm.us/patents/RE44175/description.html</feedburner:origLink></item>
<item>
			         <title><![CDATA[Pattern correcting method, mask forming method, and method of manufacturing semiconductor device]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/srKarPzMTZQ/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8443310&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; ; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;A pattern correcting method of an embodiment computes a distribution of pattern coverages on a design layout of a circuit pattern in the vicinity of a position that becomes an error pattern in a case where an on-substrate pattern is formed. Then, an area on the design layout in which a difference in the distribution of the pattern coverages becomes small by adding an addition pattern is set as an addition area. Next, addition pattern candidates to be added to the addition area are ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/srKarPzMTZQ" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8443310</guid>			
			      <feedburner:origLink>http://www.patentstorm.us/patents/8443310/description.html</feedburner:origLink></item>
<item>
			         <title><![CDATA[Method and apparatus for high acid content feed for making diesel and aviation fuel]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/ua0vnUF8hhQ/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440875&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventor:&lt;/strong&gt; &amp;nbsp;&lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;A method of making a diesel fuel from a renewable feedstock is described. Ammonia or an amine compound is used to neutralize the organic acids in the renewable feedstock. The ammonia or amine compound is removed from the product mixture before the isomerization zone so that it does not affect the isomerization ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/ua0vnUF8hhQ" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440875</guid>			
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			         <title><![CDATA[Olefin isomerization and metathesis catalyst]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/GcpadWRtrBQ/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440874&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; ; ; ; ; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;A process for the production of propylene, the process including: contacting ethylene and a hydrocarbon stream comprising 1-butene and 2-butene with a bifunctional isomerization-metathesis catalyst to concurrently isomerizes 1-butene to 2-butene and to form a metathesis product comprising propylene; wherein the bifunctional isomerization-metathesis catalyst comprises: a catalyst compound may include at least one element selected from tungsten, tantalum, niobium, molybdenum, nickel, ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/GcpadWRtrBQ" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440874</guid>			
			      <feedburner:origLink>http://www.patentstorm.us/patents/8440874/description.html</feedburner:origLink></item>
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			         <title><![CDATA[Process for producing olefins]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/xn9BPEbEJM0/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440873&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; ; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;Process for producing mono-olefins(s) from a feedstock A containing ethanol and propanol, wherein ethanol and propanol are dehydrated into the corresponding same carbon number olefins. The process is performed by 1. reacting feedstock A in a vapor phase dehydration reactor wherein the ethanol and propanol alcohols are converted into a product stream B comprising ethylene, propylene, ethers, water and unconverted alcohols, 2. cooling the product stream B, 3. disengaging the cooled product ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/xn9BPEbEJM0" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440873</guid>			
			      <feedburner:origLink>http://www.patentstorm.us/patents/8440873/description.html</feedburner:origLink></item>
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			         <title><![CDATA[Process for preparing poly alpha olefins and lubricant basestocks from Fischer-Tropsch liquids]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/wt8K1I4bv64/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440872&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; ; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;A process for preparing poly alpha olefins from a Fisher-Tropsch product. The process comprising the steps of contacting a C&lt;sub&gt;5&lt;/sub&gt;-C&lt;sub&gt;18 &lt;/sub&gt;fraction of an alpha-olefinic hydrocarbon mixture produced from thermal cracking a C&lt;sub&gt;16&lt;/sub&gt;-C&lt;sub&gt;40 &lt;/sub&gt;Fisher-Tropsch product with an oligomerization catalyst under conditions to produce an oligomerized product; and fractionating the oligomerized product to obtain a fractionated product having an average carbon number greater than ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/wt8K1I4bv64" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440872</guid>			
			      <feedburner:origLink>http://www.patentstorm.us/patents/8440872/description.html</feedburner:origLink></item>
<item>
			         <title><![CDATA[Tetramer production apparatus and process relating thereto]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/rKiRhcQj4ZA/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440871&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventor:&lt;/strong&gt; &amp;nbsp;&lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;One exemplary embodiment can be a tetramer production apparatus. The apparatus can include a fractionation zone and an oxygenate removal zone. The fractionation zone can produce a distillation product including one or more C6 hydrocarbons for producing one or more C12 compounds. The oxygenate removal zone may remove one or more oxygenate compounds from the distillation product passed through the oxygenate removal ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/rKiRhcQj4ZA" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440871</guid>			
			      <feedburner:origLink>http://www.patentstorm.us/patents/8440871/description.html</feedburner:origLink></item>
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			         <title><![CDATA[One-step catalytic conversion of biomass-derived carbohydrates to liquid fuels]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/m61QiIbPze0/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440870&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventor:&lt;/strong&gt; &amp;nbsp;&lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;The invention relates to a method for manufacture of hydrocarbon fuels and oxygenated hydrocarbon fuels such as alkyl substituted tetrahydrofurans such as 2,5-dimethyltetrahydrofuran, 2-methyltetrahydrofuran and mixtures thereof. The method generally entails forming a mixture of reactants that includes carbonaceous material water, a metal catalyst and an acid reacting that mixture in the presence of hydrogen. The reaction is performed at a temperature and for a time sufficient to produce a ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/m61QiIbPze0" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440870</guid>			
			      <feedburner:origLink>http://www.patentstorm.us/patents/8440870/description.html</feedburner:origLink></item>
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			         <title><![CDATA[Use of ionic liquids containing tricyanomethide anions as solvents for the extraction of alcohols from aqueous solutions]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/GWQm59jzs-4/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440869&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; ; ; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;The invention relates to a method for the liquid-liquid extraction of alcohols from aqueous solutions using at least one ionic liquid containing a tricyanomethide anion as ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/GWQm59jzs-4" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440869</guid>			
			      <feedburner:origLink>http://www.patentstorm.us/patents/8440869/description.html</feedburner:origLink></item>
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			         <title><![CDATA[Manufacture of methanol]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/-rq78XKo8DU/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440868&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventor:&lt;/strong&gt; &amp;nbsp;&lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;An alcohol such as methanol is produced from an alkane such as methane and oxygen in a single step process using a heterogeneous catalyst. The catalyst comprises the chloride salts of copper, potassium, lead and ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/-rq78XKo8DU" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440868</guid>			
			      <feedburner:origLink>http://www.patentstorm.us/patents/8440868/description.html</feedburner:origLink></item>
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			         <title><![CDATA[Process for producing ethanol from syngas]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/32zqaktnT1Y/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440867&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; ; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;The invention provides a method for producing ethanol, the method comprising establishing an atmosphere containing methanol forming catalyst and ethanol forming catalyst; injecting syngas into the atmosphere at a temperature and for a time sufficient to produce methanol; and contacting the produced methanol with additional syngas at a temperature and for a time sufficient to produce ethanol. The invention also provides an integrated system for producing methanol and ethanol from syngas, the ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/32zqaktnT1Y" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440867</guid>			
			      <feedburner:origLink>http://www.patentstorm.us/patents/8440867/description.html</feedburner:origLink></item>
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			         <title><![CDATA[Process for separating ethanol having low acid]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/LpXtWhqmGbc/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440866&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;A process for operating a distillation column to separate an ethanol mixture comprising ethanol and acetic acid where the recovered ethanol comprises less than 700 wppm acetic acid. The operating conditions for the column may vary depending on the fed composition. In particular the process provides energy efficient recovery of ethanol with low concentration acetic ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/LpXtWhqmGbc" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440866</guid>			
			      <feedburner:origLink>http://www.patentstorm.us/patents/8440866/description.html</feedburner:origLink></item>
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			         <title><![CDATA[Process for the manufacture of alkenones]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/od8YbwNRY58/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440865&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; ; ; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;Process for preparing an alkenone, which comprises the following steps: (a) providing a halogenated precursor of the alkenone; and (b) eliminating the hydrogen halide from said precursor to form the alkenone by a thermolysis treatment selected from the group consisting of flash thermolysis, vacuum thermolysis, and thermolysis under stripping with inert ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/od8YbwNRY58" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440865</guid>			
			      <feedburner:origLink>http://www.patentstorm.us/patents/8440865/description.html</feedburner:origLink></item>
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			         <title><![CDATA[Process for producing sec-butylbenzene]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/umYLBsB8WD4/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440864&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; ; ; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;In a process for producing sec-butylbenzene, a C&lt;sub&gt;4 &lt;/sub&gt;olefinic hydrocarbon feedstock comprising isobutene and at least one n-butene is contacted with methanol and/or water in the presence of an acid catalyst to selectively oxygenate isobutene to produce an effluent stream rich in n-butene and containing less isobutene than the feedstock. The effluent stream is then contacted with benzene under alkylation conditions and in the presence of an alkylation catalyst to produce alkylation ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/umYLBsB8WD4" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440864</guid>			
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			         <title><![CDATA[Preparation of (2R,3R)-3-(3-methoxyphenyl)-N,N,2-trimethylpentanamine]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/RKeQ_jLlDI0/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440863&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;The present invention relates to an improved process for the preparation of (2R,3R)-3-(3-methoxyphenyl)-N,N,2-trimethylpentanamine which is an intermediate for the preparation of the analgesic ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/RKeQ_jLlDI0" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440863</guid>			
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			         <title><![CDATA[Process for preparing β-amino-α-hydroxycarboxamides]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/TmSdqRzKWd8/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440862&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventor:&lt;/strong&gt; &amp;nbsp;&lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;The present invention is directed to a process for preparing β-amino-α-hydroxycarboxamides. The process works with epoxycarboxamides of the formula 2&lt;/p&gt;
&lt;p&gt;&lt;chemistry&gt;

&lt;/chemistry&gt;
&lt;br&gt;&lt;/br&gt;
which are reacted with ammonia or other ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/TmSdqRzKWd8" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440862</guid>			
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			         <title><![CDATA[Solid forms of an -(phenylmethyl)propanamide derivative and processes of preparation]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/kswgLKIG0fA/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440861&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; ; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;The invention relates to solid forms of the anti-epileptic agent lacosamide (I). The invention also relates to mixtures of solid forms of lacosamide. The invention further relates to mixtures of lacosamide enantiomers crystallized in a conglomerate Form and the use thereof in providing enantiomerically enriched lacosamide, preferably lacosamide enriched with the (R)-enantiomer of ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/kswgLKIG0fA" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440861</guid>			
			      <feedburner:origLink>http://www.patentstorm.us/patents/8440861/description.html</feedburner:origLink></item>
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			         <title><![CDATA[Process for manufacturing N, N-dialkyl lactamide]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/tHpGCfetUyQ/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440860&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventor:&lt;/strong&gt; &amp;nbsp;&lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;A process for manufacturing dialkyl lactamide including reacting lactide and dialkylamine selected from one or more of dimethylamine, diethylamine, and methylethylamine to form a reaction mixture which includes dialkyl lactamide selected from N,N-dimethyl lactamide, N,N-diethyl lactamide, and N,N-methylethyl lactamide, N,N-dialkyl lactoyl lactamide, and dialkylamine, subjecting the reaction mixture to a separation step to form a product stream including N,N-dialkyl lactamide, a first ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/tHpGCfetUyQ" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440860</guid>			
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<item>
			         <title><![CDATA[Method for producing bioresourced propionic acid from glycerol]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/abpIr1xbqNc/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440859&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventor:&lt;/strong&gt; &amp;nbsp;&lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;The invention relates to a method for producing bioresourced propionic acid from glycerol. The invention also relates to a composition comprising more than 85 mass % of bioresourced propionic acid, and to the use of the propionic acid obtained from the method as a solvent, as a food preservative, for producing herbicide or for preparing vinyl ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/abpIr1xbqNc" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440859</guid>			
			      <feedburner:origLink>http://www.patentstorm.us/patents/8440859/description.html</feedburner:origLink></item>
<item>
			         <title><![CDATA[Method of making fluorinated alkoxy carboxylic acids and precursors thereof]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/LGFBHwaYLkw/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440858&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; ; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;A method for preparing saturated partially fluorinated alkoxy carboxylic acids or salts thereof by treating a compound: (II), where R&lt;sub&gt;f &lt;/sub&gt;represents a fluorinated, linear or branched alkyl residue interruptible by one or more oxygen atoms, n is 0 or 1, with a Z-anion in a reaction medium comprising water and an organic solvent, where the Z-anion is selected from CN—, SCN— and OCN— or combinations thereof. A method of making partially fluorinated ethers of the general formula ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/LGFBHwaYLkw" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440858</guid>			
			      <feedburner:origLink>http://www.patentstorm.us/patents/8440858/description.html</feedburner:origLink></item>
<item>
			         <title><![CDATA[Sulfonate- or sulfate-capped anti-misting agents]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/gKcmd8wvwAU/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440857&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; ; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;Sulfonate- or sulfate-capped, alkoxylated anti-misting agents having the structures: R((AO)&lt;sub&gt;n&lt;/sub&gt;X)&lt;sub&gt;m&lt;/sub&gt;((AO)&lt;sub&gt;n&lt;/sub&gt;H)&lt;sub&gt;p &lt;/sub&gt;and R&lt;sup&gt;3&lt;/sup&gt;C(O)NH(CH&lt;sub&gt;2&lt;/sub&gt;)&lt;sub&gt;z&lt;/sub&gt;N&lt;sup&gt;+&lt;/sup&gt;(CH&lt;sub&gt;3&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt;CH&lt;sub&gt;2&lt;/sub&gt;CHR&lt;sup&gt;4&lt;/sup&gt;CH&lt;sub&gt;2&lt;/sub&gt;SO&lt;sub&gt;3&lt;/sub&gt;&lt;sup&gt;−&lt;/sup&gt;, and to methods of suppressing mist from electrolyte solutions by adding a mist-suppressing amount of one or more of said compounds to electrolyte ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/gKcmd8wvwAU" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440857</guid>			
			      <feedburner:origLink>http://www.patentstorm.us/patents/8440857/description.html</feedburner:origLink></item>
<item>
			         <title><![CDATA[Method for treating residues from the production of isocyanates]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/dCMScbUIAyQ/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440856&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; ; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;This invention relates to a process for working up residues from production of isocyanates. This process involves hydrolyzing residues from production of at least one isocyanate with water to form a hydrolysis product, and processing the hydrolysis product within an extruder or a kneader having a heat transfer surface, to form a mixed product containing at least one amine and water. The amine and the water are separated from the mixed product to form an amine/water mixture, which is then ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/dCMScbUIAyQ" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440856</guid>			
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<item>
			         <title><![CDATA[Process for the production of acetic acid ethylene and vinyl acetate monomer]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/Hyffdg--2Rg/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440855&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; ; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;An integrated process for the production of acetic acid, ethylene and vinyl acetate monomer comprising the steps of:
&lt;ul&gt;
    &lt;li&gt;(a) evaporating at least part of an ethanol feed stock&lt;/li&gt;
    &lt;li&gt;(b) producing in a first reaction zone a first product stream comprising acetic acid by oxidative or partly oxidative dehydrogenation of ethanol feed stock;&lt;/li&gt;
    &lt;li&gt;(c) producing in a second reaction zone a second product stream comprising ethylene from an ethanol feed stock;&lt;/li&gt;
    ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/Hyffdg--2Rg" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440855</guid>			
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<item>
			         <title><![CDATA[Antioxidant inflammation modulators: oleanolic acid derivatives with amino acid and other modifications at C-17]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/R3CYttEF8YY/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440854&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; ; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;This invention provides, but is not limited to, novel oleanolic acid derivatives having the formula:&lt;/p&gt;
&lt;p&gt;&lt;chemistry&gt;

&lt;/chemistry&gt;
&lt;br&gt;&lt;/br&gt;
wherein the variables are defined herein. Also provided are pharmaceutical compositions, kits and articles of manufacture comprising such compounds, methods and intermediates useful for making the compounds, and methods of using the compounds and ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/R3CYttEF8YY" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440854</guid>			
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<item>
			         <title><![CDATA[Ester compound and use thereof]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/HAk5OYJuG1Y/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440853&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventor:&lt;/strong&gt; &amp;nbsp;&lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;An ester compound represented by formula (1):
&lt;ul&gt;
    &lt;li&gt;wherein R&lt;sup&gt;2 &lt;/sup&gt;represents hydrogen, fluorine, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 alkoxymethyl, or C1-C4 alkylthiomethyl; and R&lt;sup&gt;2 &lt;/sup&gt;represents C&lt;sub&gt;1&lt;/sub&gt;-C&lt;sub&gt;4 &lt;/sub&gt;alkyl,&lt;/li&gt;
    &lt;li&gt;has an excellent pest control effect and is therefore useful as an active ingredient of a pest control ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/HAk5OYJuG1Y" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440853</guid>			
			      <feedburner:origLink>http://www.patentstorm.us/patents/8440853/description.html</feedburner:origLink></item>
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			         <title><![CDATA[Method for producing tetraethylenepentamine]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/kSdJQKL3aQA/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440852&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; ; ; ; ; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;The invention relates to a process for preparing tetraethylenepentamine (TEPA) by hydrogenation of diethylenetriaminediacetonitrile (DETDN) over a catalyst. If appropriate, DETDN can also be present as a constituent of an amino nitrile mixture which additionally comprises diethylenetriaminemonoacetonitrile ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/kSdJQKL3aQA" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440852</guid>			
			      <feedburner:origLink>http://www.patentstorm.us/patents/8440852/description.html</feedburner:origLink></item>
<item>
			         <title><![CDATA[Spatially-defined macrocyclic compounds useful for drug discovery]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/lSAKgr9Ht80/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440851&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; ; ; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;Novel spatially-defined macrocyclic compounds containing specific conformational control elements are disclosed. Libraries of these macrocycles are then used to select one or more macrocycle species that exhibit a specific interaction with a particular biological target. In particular, compounds according to the invention are disclosed as agonists or antagonists of a mammalian motilin receptor and a mammalian ghrelin ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/lSAKgr9Ht80" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440851</guid>			
			      <feedburner:origLink>http://www.patentstorm.us/patents/8440851/description.html</feedburner:origLink></item>
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			         <title><![CDATA[Polyarylacetylenes containing siloxane, silane, and carborane moieties]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/dHSNuDvKZMY/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440850&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;Disclosed herein are the compounds shown below. Each R is an organic group, Cb is a carborane group, and —C&lt;sub&gt;6&lt;/sub&gt;H&lt;sub&gt;4&lt;/sub&gt;— is phenylene. The value of each m is a nonnegative integer, q is 0 or 1, with the proviso that if q is 0 then m is 0 or 1, p is a positive integer, r is a positive integer, and n is an integer greater than or equal to 10. Also disclosed are methods of making and crosslinking the ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/dHSNuDvKZMY" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440850</guid>			
			      <feedburner:origLink>http://www.patentstorm.us/patents/8440850/description.html</feedburner:origLink></item>
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			         <title><![CDATA[Use of nitroaniline derivatives for the production of nitric oxide]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/2s_slyXDutk/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440849&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;The present disclosure relates to the use of a nitroaniline derivative of Formula (I) for the production of nitric oxide and for the preparation of a medicament for the treatment of a disease wherein the administration of nitric oxide is beneficial. The present disclosure furthermore relates to a method for the production of NO irradiating a nitroaniline derivative of Formula (I), a kit comprising a nitroaniline derivative of Formula (I) and a carrier and to a system comprising a source of ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/2s_slyXDutk" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440849</guid>			
			      <feedburner:origLink>http://www.patentstorm.us/patents/8440849/description.html</feedburner:origLink></item>
<item>
			         <title><![CDATA[Polyorganosiloxane composition, cured product of the composition, and method for producing the composition]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/yHpts6TdD2k/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440848&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; ; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;Disclosed is an organosiloxane composition which can be produced at low cost and is usable for bonding of glasses, metals and resins. The organosiloxane composition can provide a cured product exhibiting excellent heat resistance and cold resistance, while having high strength and high transparency. Specifically disclosed is a polyorganosiloxane composition containing (A) a polyorganosiloxane wherein at least one end of each molecule is modified with a silanol group, and (B) 0.5-4.0 moles ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/yHpts6TdD2k" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440848</guid>			
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<item>
			         <title><![CDATA[Method of converting free fatty acid (FFA) from oil to methyl ester]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/CB5V4924mlg/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440847&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventor:&lt;/strong&gt; &amp;nbsp;&lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;The present invention provides a method of converting free fatty acid (FFA) from oil to methyl ester, the method includes the steps (a) esterifying the FFA using an acidic catalyst dissolved in an alcohol, (b) separating excess alcohol, solid acid catalyst, water, glycerol, soap and other non-lipid soluble impurities from oil obtained from step (a), (c) neutralizing the oil from step (b), (d) drying the oil from step (c) and (e) transesterifying the oil from step (d) using an alkaline ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/CB5V4924mlg" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440847</guid>			
			      <feedburner:origLink>http://www.patentstorm.us/patents/8440847/description.html</feedburner:origLink></item>
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			         <title><![CDATA[Direct epoxidation process]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/R44xAGJZuPg/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440846&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; ; ; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;The invention is a process for epoxidizing an olefin with hydrogen and oxygen in a solvent comprising acetonitrile in the presence of an quinone-acid salt and a catalyst comprising a titanium zeolite and a noble metal. The process results in higher productivity and improved selectivity to propylene oxide from hydrogen and oxygen, as compared to processes that use only a ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/R44xAGJZuPg" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440846</guid>			
			      <feedburner:origLink>http://www.patentstorm.us/patents/8440846/description.html</feedburner:origLink></item>
<item>
			         <title><![CDATA[Process for converting polysaccharides in an inorganic molten salt hydrate]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/sV11k176KJ8/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440845&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; ; ; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;A process is disclosed for converting a polysaccharide-containing biomass material to platform chemicals.&lt;/p&gt;
&lt;p&gt;The process comprises dissolving the polysaccharides in an inorganic molten salt hydrate, converting the polysaccharides to monosaccharides, and converting the monosaccharides to derivatized (di)anhydro sugars that are easily separable from the inorganic molten salt hydrate.&lt;/p&gt;
&lt;p&gt;The derivatized (di)anhydro sugars are useful as fuel additives and fuel ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/sV11k176KJ8" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440845</guid>			
			      <feedburner:origLink>http://www.patentstorm.us/patents/8440845/description.html</feedburner:origLink></item>
<item>
			         <title><![CDATA[Process for the preparation of β-amino alcohol]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/Yd-R5KB56tM/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440844&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;A high-yielding enantioselective synthesis of the bioactive (S)—N-(5-chlorothiophene-2-sulfonyl)-β,β-diethylalaniol (7.b.2), a Notch-1-sparing γ-secretase inhibitor metabolite (with EC&lt;sub&gt;50&lt;/sub&gt;=28 nM) effective in reduction of Aβ production in vivo, has been realized starting from readily available 3-pentanone. The key steps of the synthesis are proline-catalyzed α-aminooxylation and α-amination of aldehyde; the latter contributing an overall yield of 50-75% and 90-99% ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/Yd-R5KB56tM" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440844</guid>			
			      <feedburner:origLink>http://www.patentstorm.us/patents/8440844/description.html</feedburner:origLink></item>
<item>
			         <title><![CDATA[2, 2-bipyridine ligand, sensitizing dye and dye sensitized solar cell]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/am886Si6boo/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440843&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; ; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;A dye sensitized solar cell, comprising a heteroleptic polypyridil complex of Ru, Os or Fe. The donating ligand has an extended conjugated π-system increasing the light absorbance and keeing the LUMO energy level higher than that of the anchoring ligand. A compacting compound whose molecular structure comprises a terminal group, a hydrophobic part and an anchoring group may be co-adsorbed together with the dye on the semi-conductive metal oxide layer of the photoanode, forming a dense ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/am886Si6boo" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440843</guid>			
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<item>
			         <title><![CDATA[Antimicrobial compounds, their synthesis and their use for treatment of mammalian infections]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/iLlPWkQaX5M/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440842&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; ; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;The present invention relates to compounds of Formula (I)&lt;/p&gt;
&lt;p&gt;&lt;chemistry&gt;

&lt;/chemistry&gt;
&lt;br&gt;&lt;/br&gt;
or salts thereof wherein R&lt;sup&gt;1&lt;/sup&gt;, R&lt;sup&gt;2&lt;/sup&gt;, R&lt;sup&gt;3&lt;/sup&gt;, R&lt;sup&gt;4&lt;/sup&gt;, R&lt;sup&gt;5&lt;/sup&gt;, R&lt;sup&gt;6&lt;/sup&gt;, and other variables enumerated under one or more of same are as defined herein. Compounds of Formula I have activity as antimicrobial agents. Also disclosed are pharmaceutical compositions and methods of treating and preventing microbial infections in mammals, for example, a ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/iLlPWkQaX5M" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440842</guid>			
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<item>
			         <title><![CDATA[5-pyrrolidinylsulfonyl isatin derivatives]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/HNdvPZME-oM/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440841&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;The present invention relates to novel 5-pyrrolidinylsulfonyl isatin derivatives, non-peptidyl Caspase binding Radioligands (CbRs) and CbR-transporter conjugates derived from said isatin derivatives, diagnostic compositions comprising said compounds of the invention and their use for non-invasive diagnostic ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/HNdvPZME-oM" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440841</guid>			
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<item>
			         <title><![CDATA[Dye including an anchoring group in its molecular structure]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/pv1ChA7SNH4/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440840&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;A dye including an anchoring group in its molecular structure, said anchoring group allowing a covalent coupling of said dye to a surface, for example a surface of a nanoporous semiconductor layer, said anchoring group being represented by formula 1 wherein attachment of said anchoring group within said molecular structure of said dye is at the terminal carbon marked with an asterisk in above formula, wherein G is selected from —COOH, —SO3H, —PO3H2, —BO2H2, —SH, —OH, —NH2, ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/pv1ChA7SNH4" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440840</guid>			
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<item>
			         <title><![CDATA[Dinitropyrazole derivatives, their preparation, and energetic compositions comprising them]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/yJSDQrycAo0/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440839&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventor:&lt;/strong&gt; &amp;nbsp;&lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;The present invention provides:
&lt;ul&gt;
    &lt;li&gt;dinitropyrazole derivatives of formula (I)&lt;/li&gt;
&lt;/ul&gt;
&lt;/p&gt;
&lt;p&gt;&lt;chemistry&gt;

&lt;/chemistry&gt;
&lt;br&gt;&lt;/br&gt;
in which: R═NO&lt;sub&gt;2&lt;/sub&gt;, NH&lt;sub&gt;2&lt;/sub&gt;, NF&lt;sub&gt;2&lt;/sub&gt;, NHOH, OH or NHNH&lt;sub&gt;2 &lt;/sub&gt;and R′═H when R═NH&lt;sub&gt;2&lt;/sub&gt;, NF&lt;sub&gt;2&lt;/sub&gt;, NHOH, OH or NHNH&lt;sub&gt;2 &lt;/sub&gt;or R′═H, NH&lt;sub&gt;2 &lt;/sub&gt;or a linear or branched C&lt;sub&gt;1&lt;/sub&gt;-C&lt;sub&gt;4 &lt;/sub&gt;alkyl group, optionally substituted by at least one hydroxy and/or one fluoro group, when ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/yJSDQrycAo0" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440839</guid>			
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<item>
			         <title><![CDATA[Aryl (1H-1,2,4-triazol-1-yl) compound and process for production thereof]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/QgRvOWHbhWA/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440838&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventor:&lt;/strong&gt; &amp;nbsp;&lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;An aryl (1H-1,2,4-triazol-1-yl) compound is useful for producing a 3-(1H-1,2,4-triazol-1-yl)phenylsulfide compound (useful, e.g., as an insecticide). Also disclosed is a process for producing the compound. The aryl (1H-1,2,4-triazol-1-yl) compound is represented by the general formula (1), below, wherein R represents a C1-C6 alkyl group or a cyclic C3-C6 alkyl group; A&lt;sub&gt;1 &lt;/sub&gt;represents a hydrogen atom, an amino group, a mono(C1-C6 alkyl amino group or a di (C1-C6 alkyl) amino group; ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/QgRvOWHbhWA" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440838</guid>			
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<item>
			         <title><![CDATA[2-substituted-ethynylthiazole derivatives and uses of same]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/ZADkrsJB0og/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440837&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; ; ; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;The present invention provides 2-substituted-ethynylthiazole derivatives of formula (I):&lt;/p&gt;
&lt;p&gt;&lt;chemistry&gt;

&lt;/chemistry&gt;
&lt;br&gt;&lt;/br&gt;
wherein R&lt;sup&gt;1&lt;/sup&gt;, R&lt;sup&gt;2 &lt;/sup&gt;and X are as defined herein, or a pharmaceutically acceptable salt thereof; and pharmaceutical compositions and methods of using ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/ZADkrsJB0og" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440837</guid>			
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<item>
			         <title><![CDATA[Heterocyclic alkanol derivatives]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/n4sHFQSmeVE/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440836&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; ; ; ; ; ; ; ; ; ; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;The present invention relates to novel heterocyclic alkanol derivatives, to processes for preparing these compounds, to compositions comprising these compounds and to their use as biologically active compounds, in particular for controlling harmful microorganisms in crop protection and in the protection of materials and as plant growth ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/n4sHFQSmeVE" height="1" width="1"/&gt;</description>			         
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<item>
			         <title><![CDATA[Environmentally sensitive fluorophores]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/BbWxFRmQeO8/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440835&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;The present invention generally relates to environment-sensitive fluorophores, including environment-sensitive fluorophores for reporting protein/protein and peptide/protein interactions. In one aspect, the present invention is directed to compounds and salts thereof, compositions and methods useful in determining biological interactions. In some cases, the compounds of the present invention are environment-sensitive fluorophores that have spectroscopic behavior that may depend on factors ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/BbWxFRmQeO8" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440835</guid>			
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			         <title><![CDATA[1-phenyl-2-pyridinyl alkyl alcohol compounds as phosphodiesterase inhibitors]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/I96_bTYe5-g/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440834&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventor:&lt;/strong&gt; &amp;nbsp;&lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;1-Phenyl-2-pyridinyl alkyl alcohol compounds are effective as inhibitors of the phosphodiesterase 4 (PDE4) enzyme and may be used to prevent and/or treat certain diseases or ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/I96_bTYe5-g" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440834</guid>			
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			         <title><![CDATA[Human papilloma virus inhibitors and pharmaceutical compositions containing same]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/VrUyzsLkq9Q/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440833&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; ; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;HPV inhibitors of formula (I) in which G&lt;sub&gt;1 &lt;/sub&gt;is —NHCO(CH&lt;sub&gt;2&lt;/sub&gt;)n-, where n is an integer between 1 and 4, R3 is —CW(CH&lt;sub&gt;2&lt;/sub&gt;)&lt;sub&gt;m&lt;/sub&gt;—NR4R5 or —CW(CH&lt;sub&gt;2&lt;/sub&gt;)&lt;sub&gt;m&lt;/sub&gt;CH&lt;sub&gt;3 &lt;/sub&gt;or —CN, where W is O, S or NH and m is an integer between 0 and 5, or R3 is one of the following groups: and A is an optionally substituted aryl group and B is an aryl group, preferably a phenyl which is ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/VrUyzsLkq9Q" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440833</guid>			
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<item>
			         <title><![CDATA[Heterocyclic modulators of cannabinoid receptors]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/A1uZPnldr4w/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440832&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;Heterocyclic compounds which modulate cannabinoid receptors are presented. Pharmaceutical compositions containing these compounds, methods of using these compounds as modulators of cannabinoid receptors and processes for synthesizing these compounds are also described ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/A1uZPnldr4w" height="1" width="1"/&gt;</description>			         
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<item>
			         <title><![CDATA[Process and intermediates for preparing integrase inhibitors]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/W3sFMQmqFWY/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440831&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;The invention provides synthetic processes and synthetic intermediates that can be used to prepare 4-oxoquinolone compounds having useful integrase inhibiting ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/W3sFMQmqFWY" height="1" width="1"/&gt;</description>			         
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<item>
			         <title><![CDATA[Tetrahydro-fused pyridines as histone deacetylase inhibitors]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/0_QzAXIgbPs/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440830&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; ; ; ; ; ; ; ; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;The compounds of formula (I), wherein ring D and ring E together form a fused ring system selected from formula (II), (III), (IV), (V), (VI), (VII), and the salts of these compounds are novel, effective inhibitors of histone ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/0_QzAXIgbPs" height="1" width="1"/&gt;</description>			         
			         <guid isPermaLink="false">8440830</guid>			
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<item>
			         <title><![CDATA[PI3 kinase/mTOR dual inhibitor]]></title>
			         <link>http://feedproxy.google.com/~r/Patentstorm-Patents-Chemistry/~3/Yu9BrkNJBmc/description.html</link>
			         <description>&lt;ul&gt;&lt;li&gt;&lt;strong&gt;Patent Number:&lt;/strong&gt; &amp;nbsp;8440829&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Publication Date:&lt;/strong&gt; &amp;nbsp;2013-05-14&lt;/li&gt;&lt;li&gt;&lt;strong&gt;Inventors:&lt;/strong&gt; &amp;nbsp;; &lt;/li&gt;&lt;/ul&gt;
&lt;p&gt;The present invention provides an imidazo[4,5-c]quinolin-2-one compound, or a pharmaceutically acceptable salt thereof, that inhibits both PI3K and mTOR and, therefore, is useful in the treatment of ...&lt;br /&gt;&lt;img src="http://feeds.feedburner.com/~r/Patentstorm-Patents-Chemistry/~4/Yu9BrkNJBmc" height="1" width="1"/&gt;</description>			         
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