Polyaniline-Supported Sulfuric Acid Salt as a Powerful Catalyst for the Protection and Deprotection of Carbonyl Compounds
Abstract Structurally different carbonyl compounds were converted into their corresponding cyclic acetals using polyaniline-sulfate salt as catalyst in dry toluene in excellent yield. In turn, useful deacetalization in aqueous medium was demonstrated. Chemoselective protection of carbonyl compounds...
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Veröffentlicht in: | Synlett 2003-09, Vol.2003 (12), p.1793-1796 |
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container_issue | 12 |
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container_title | Synlett |
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creator | Palaniappan, Srinivasan Narender, Puli Saravanan, Chandrasekaran Rao, Vaidya Jayathirtha |
description | Abstract
Structurally different carbonyl compounds were converted into their corresponding cyclic acetals using polyaniline-sulfate salt as catalyst in dry toluene in excellent yield. In turn, useful deacetalization in aqueous medium was demonstrated. Chemoselective protection of carbonyl compounds was also demonstrated. The advantages of the polyaniline-sulfate salt are ease of preparation and handling, stability, reusability and activity. |
doi_str_mv | 10.1055/s-2003-41412 |
format | Article |
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Structurally different carbonyl compounds were converted into their corresponding cyclic acetals using polyaniline-sulfate salt as catalyst in dry toluene in excellent yield. In turn, useful deacetalization in aqueous medium was demonstrated. Chemoselective protection of carbonyl compounds was also demonstrated. The advantages of the polyaniline-sulfate salt are ease of preparation and handling, stability, reusability and activity.</description><identifier>ISSN: 0936-5214</identifier><identifier>EISSN: 1437-2096</identifier><identifier>DOI: 10.1055/s-2003-41412</identifier><language>eng</language><subject>letter</subject><ispartof>Synlett, 2003-09, Vol.2003 (12), p.1793-1796</ispartof><rights>Georg Thieme Verlag Stuttgart · New York</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c269t-75c38998845c871ff98913ed6b565332e70ce30735c391e7f8fa3a844b063bda3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-2003-41412.pdf$$EPDF$$P50$$Gthieme$$H</linktopdf><linktohtml>$$Uhttps://www.thieme-connect.de/products/ejournals/html/10.1055/s-2003-41412$$EHTML$$P50$$Gthieme$$H</linktohtml><link.rule.ids>314,777,781,3004,3005,27905,27906,54540,54541</link.rule.ids></links><search><creatorcontrib>Palaniappan, Srinivasan</creatorcontrib><creatorcontrib>Narender, Puli</creatorcontrib><creatorcontrib>Saravanan, Chandrasekaran</creatorcontrib><creatorcontrib>Rao, Vaidya Jayathirtha</creatorcontrib><title>Polyaniline-Supported Sulfuric Acid Salt as a Powerful Catalyst for the Protection and Deprotection of Carbonyl Compounds</title><title>Synlett</title><addtitle>Synlett</addtitle><description>Abstract
Structurally different carbonyl compounds were converted into their corresponding cyclic acetals using polyaniline-sulfate salt as catalyst in dry toluene in excellent yield. In turn, useful deacetalization in aqueous medium was demonstrated. Chemoselective protection of carbonyl compounds was also demonstrated. The advantages of the polyaniline-sulfate salt are ease of preparation and handling, stability, reusability and activity.</description><subject>letter</subject><issn>0936-5214</issn><issn>1437-2096</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNptkNFKwzAUhoMoOKd3PkDutZo0SZtcjulUGDiYXpc0PWEdWVOSFOnb2znBG68O5-f7D4cPoVtKHigR4jFmOSEs45TT_AzNKGfllKjiHM2IYkUmcsov0VWMe0Iol4rM0LjxbtRd69oOsu3Q9z4kaPB2cHYIrcEL006bdgnriDXe-C8IdnB4qZN2Y0zY-oDTDvAm-AQmtb7DumvwE_R_gbcTH2rfjVPRH3o_dE28RhdWuwg3v3OOPlfPH8vXbP3-8rZcrDOTFyplpTBMKiUlF0aW1FolFWXQFLUoBGM5lMQAIyWbOEWhtNJqpiXnNSlY3Wg2R_enuyb4GAPYqg_tQYexoqQ6aqtiddRW_Wib8LsTnnYtHKDa-yF003__098EiW7Y</recordid><startdate>20030929</startdate><enddate>20030929</enddate><creator>Palaniappan, Srinivasan</creator><creator>Narender, Puli</creator><creator>Saravanan, Chandrasekaran</creator><creator>Rao, Vaidya Jayathirtha</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20030929</creationdate><title>Polyaniline-Supported Sulfuric Acid Salt as a Powerful Catalyst for the Protection and Deprotection of Carbonyl Compounds</title><author>Palaniappan, Srinivasan ; Narender, Puli ; Saravanan, Chandrasekaran ; Rao, Vaidya Jayathirtha</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c269t-75c38998845c871ff98913ed6b565332e70ce30735c391e7f8fa3a844b063bda3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>letter</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Palaniappan, Srinivasan</creatorcontrib><creatorcontrib>Narender, Puli</creatorcontrib><creatorcontrib>Saravanan, Chandrasekaran</creatorcontrib><creatorcontrib>Rao, Vaidya Jayathirtha</creatorcontrib><collection>CrossRef</collection><jtitle>Synlett</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Palaniappan, Srinivasan</au><au>Narender, Puli</au><au>Saravanan, Chandrasekaran</au><au>Rao, Vaidya Jayathirtha</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polyaniline-Supported Sulfuric Acid Salt as a Powerful Catalyst for the Protection and Deprotection of Carbonyl Compounds</atitle><jtitle>Synlett</jtitle><addtitle>Synlett</addtitle><date>2003-09-29</date><risdate>2003</risdate><volume>2003</volume><issue>12</issue><spage>1793</spage><epage>1796</epage><pages>1793-1796</pages><issn>0936-5214</issn><eissn>1437-2096</eissn><abstract>Abstract
Structurally different carbonyl compounds were converted into their corresponding cyclic acetals using polyaniline-sulfate salt as catalyst in dry toluene in excellent yield. In turn, useful deacetalization in aqueous medium was demonstrated. Chemoselective protection of carbonyl compounds was also demonstrated. The advantages of the polyaniline-sulfate salt are ease of preparation and handling, stability, reusability and activity.</abstract><doi>10.1055/s-2003-41412</doi><tpages>4</tpages></addata></record> |
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title | Polyaniline-Supported Sulfuric Acid Salt as a Powerful Catalyst for the Protection and Deprotection of Carbonyl Compounds |
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