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		    <title>PatentStorm -> Patents -> Organic compounds -- part of the class 532-570 series</title>
		    <link>http://www.patentstorm.us/rss/class/patents/rss-564.xml</link>
		    <description>Recent patents filings in USPTO Class 564 Organic compounds -- part of the class 532-570 series.</description>
		    <pubDate>Tue, 7 Feb 2012 16:02:56</pubDate>
		    <managingEditor>patents@patentstorm.us</managingEditor>
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			         <title><![CDATA[Surfactant]]></title>
			         <link>http://www.patentstorm.us/patents/8110707/description.html</link>
			         <description><![CDATA[<ul><li><strong>Patent Number:</strong> &nbsp;8110707</li><li><strong>Publication Date:</strong> &nbsp;2012-02-07</li><li><strong>Inventors:</strong> &nbsp;Uenishi, Katsuya; Iwase, Toshiaki; Kuroiwa, Jun; Yoshida, Masanori; Murayama, Kouei</li></ul>
<p>A fatty acid salt of an alkyl quaternary ammonium is used as a novel surfactant which is a cationic surfactant having high detergency and low foaming ...<br /> 		
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			         <title><![CDATA[Formoterol tartrate process and polymorph]]></title>
			         <link>http://www.patentstorm.us/patents/8110706/description.html</link>
			         <description><![CDATA[<ul><li><strong>Patent Number:</strong> &nbsp;8110706</li><li><strong>Publication Date:</strong> &nbsp;2012-02-07</li><li><strong>Inventors:</strong> &nbsp;Tanoury, Gerald J.; Senanayake, Chris H.; Kessler, Donald W.</li></ul>
<p>A method of preparation of a highly pure salt of R,R-formoterol L-tartrate is disclosed. The process provides the most thermodynamically stable polymorph by recrystallization of a novel ...<br /> 		
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			         <title><![CDATA[Processes for making hydrazides]]></title>
			         <link>http://www.patentstorm.us/patents/8110705/description.html</link>
			         <description><![CDATA[<ul><li><strong>Patent Number:</strong> &nbsp;8110705</li><li><strong>Publication Date:</strong> &nbsp;2012-02-07</li><li><strong>Inventors:</strong> &nbsp;Sahli, Ayman; Chiarello, George Anello</li></ul>
<p>A method is disclosed for preparing hydrazides from hydrazine and an acyl chloride which comprises the steps of (a) preparing a stirred substantially uniform slurry comprising hydrazine and an inert solvent at low temperature; and (b) adding an acyl chloride continuously to said slurry. The method avoids or limits production of undesired bis-hydrazide by-products. The method is used to prepare 3-methyl-3-mercaptobutanoic acid hydrazide, a molecule used to link calicheamicin to a monoclonal ...<br /> 		
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			         <title><![CDATA[Process for the production of compounds via hazardous intermediates in a series of microreactors]]></title>
			         <link>http://www.patentstorm.us/patents/8106242/description.html</link>
			         <description><![CDATA[<ul><li><strong>Patent Number:</strong> &nbsp;8106242</li><li><strong>Publication Date:</strong> &nbsp;2012-01-31</li><li><strong>Inventors:</strong> &nbsp;Poechlauer, Peter; Broxterman, Quirinus Bernardus; Reintjens, Rafael Wilhelmus Elisabeth Ghislain; Kotthaus, Martina</li></ul>
<p>Multi-step process for the preparation of compounds via hazardous intermediates comprising the steps of a) preparing in a microreactor a hazardous intermediate and b) optionally performing one or more reaction steps on the hazardous intermediate in one or more additional microreactors and c) further converting the hazardous intermediate with a suitable reaction agent in a subsequent microreactor until a stable end product is ...<br /> 		
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			         <title><![CDATA[Enhanced process for the synthesis of urea]]></title>
			         <link>http://www.patentstorm.us/patents/8106241/description.html</link>
			         <description><![CDATA[<ul><li><strong>Patent Number:</strong> &nbsp;8106241</li><li><strong>Publication Date:</strong> &nbsp;2012-01-31</li><li><strong>Inventors:</strong> &nbsp;Gianazza, Alessandro; Carlessi, Lino</li></ul>
<p>An enhanced process is described for the synthesis of urea from ammonia and carbon dioxide, at a high pressure and temperature, with the formation of ammonium carbamate as intermediate, which includes a high pressure synthesis section, comprising at least one separation step by decomposition-stripping with ammonia of the non-converted ammonium carbamate, carried out in a vertical apparatus, commonly called stripper, characterized in that said step also comprises a feeding, in the lower part ...<br /> 		
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			         <title><![CDATA[Low molecular weight quaternary ammonium salt dispersants]]></title>
			         <link>http://www.patentstorm.us/patents/8101801/description.html</link>
			         <description><![CDATA[<ul><li><strong>Patent Number:</strong> &nbsp;8101801</li><li><strong>Publication Date:</strong> &nbsp;2012-01-24</li><li><strong>Inventors:</strong> &nbsp;Birau, Mihaela Maria; Goredema, Adela; Allen, C. Geoffrey; Strong, Aaron; Odell, Peter</li></ul>
<p>Disclosed is a chemical compound having the structure:</p>
<p><chemistry>

</chemistry>
<br></br>
wherein R<sub>1 </sub>is an all group, aryl group, alkylaryl group or arylalkyl group with at least 23 carbon atoms, R<sub>2 </sub>is an alkylene group, arylene group, alkyarylene group or arylalkylene group with at least 2 carbons and X is a quaternary ammonium ...<br /> 		
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			         <title><![CDATA[5,6-dihydro-1-pyridin-2-one compounds]]></title>
			         <link>http://www.patentstorm.us/patents/8101800/description.html</link>
			         <description><![CDATA[<ul><li><strong>Patent Number:</strong> &nbsp;8101800</li><li><strong>Publication Date:</strong> &nbsp;2012-01-24</li><li><strong>Inventors:</strong> &nbsp;Kucera, David; Ruebsam, Frank; Dragovich, Peter; Zhou, Yuefen; Chen, Lijian; Viertelhaus, Martin; Blatter, Fritz; Tran, Chinh V.; Murphy, Douglas E.</li></ul>
<p>The invention is directed to a 5,6-dihydro-1H-pyridin-2-one compound selected ...<br /> 		
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			         <title><![CDATA[Derivatives of N-(arylamino) sulfonamides as inhibitors of MEK]]></title>
			         <link>http://www.patentstorm.us/patents/8101799/description.html</link>
			         <description><![CDATA[<ul><li><strong>Patent Number:</strong> &nbsp;8101799</li><li><strong>Publication Date:</strong> &nbsp;2012-01-24</li><li><strong>Inventors:</strong> &nbsp;El Abdellaoui, Hassan; Barawkar, Dinesh; Chamakura, Varaprasad; Hong, Zhi; Maderna, Andreas; Vernier, Jean-Michel</li></ul>
<p>This invention concerns N—(2-arylamino) aryl sulfonamides, which are inhibitors of MEK and are useful in treatment of cancer and other hyperproliferative ...<br /> 		
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			         <title><![CDATA[Preparation of chiral amides and amines]]></title>
			         <link>http://www.patentstorm.us/patents/8097760/description.html</link>
			         <description><![CDATA[<ul><li><strong>Patent Number:</strong> &nbsp;8097760</li><li><strong>Publication Date:</strong> &nbsp;2012-01-17</li><li><strong>Inventors:</strong> &nbsp;Zhao, Hang; Koenig, Stefan G.; Vandenbossche, Charles P.; Singh, Surendra; Wilkinson, Harold Scott; Bakale, Roger P.</li></ul>
<p>This invention provides a convenient method for converting oximes into enamides. The process does not require the use of metallic reagents. Accordingly, it produces the desired compounds without the concomitant production of a large volume of metallic waste. The enamides are useful precursors to amides and amines. The invention provides a process to convert a prochiral enamide into the corresponding chiral amide. In an exemplary process, a chiral amino center is introduced during ...<br /> 		
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			         <title><![CDATA[Inflammatory cytokine release inhibitor]]></title>
			         <link>http://www.patentstorm.us/patents/8097759/description.html</link>
			         <description><![CDATA[<ul><li><strong>Patent Number:</strong> &nbsp;8097759</li><li><strong>Publication Date:</strong> &nbsp;2012-01-17</li><li><strong>Inventors:</strong> &nbsp;Nagano, Tatsuo; Sotome, Tomomi; Itai, Akiko; Muto, Susumu</li></ul>
<p>A medicament having inhibitory activity against NF-κB activation, which comprises a compound represented by the following general formula (I) or a pharmacologically acceptable salt as an active ingredient:</p>
<p><chemistry>

</chemistry>
<br></br>
wherein X represents a connecting group, A represents hydrogen atom or acetyl group, E represents an aryl group or a heteroaryl group, and ring X represents an arene or a ...<br /> 		
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			         <title><![CDATA[Isoserine derivatives for use as coagulation factor IXa inhibitors]]></title>
			         <link>http://www.patentstorm.us/patents/8097758/description.html</link>
			         <description><![CDATA[<ul><li><strong>Patent Number:</strong> &nbsp;8097758</li><li><strong>Publication Date:</strong> &nbsp;2012-01-17</li><li><strong>Inventors:</strong> &nbsp;Follmann, Markus; Goerlitzer, Jochen; Steinhagen, Henning; Schreuder, Herman</li></ul>
<p>The invention relates to the compounds of formula (I)</p>
<p><chemistry>

</chemistry>
<br></br>
having antithrombotic activity which especially inhibit blood clotting factor IXa, to methods for producing the same and to the use thereof as ...<br /> 		
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