THE CHIRAL LIGAND-CATALYZED ENANTIOSELECTIVE CONJUGATE ADDITION OF ORGANOLITHIUM TO BHA ENOATE
The conjugate addition reaction of BHA alkenoates with butyl- and phenyllithiums in toluene at -78°C were catalyzed by a substoichiometric amount of chiral ligands 1 and 2 to give the corresponding 3-substituted alkanoates in good to modest ees.
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Veröffentlicht in: | Chemical & pharmaceutical bulletin 1998/01/15, Vol.46(1), pp.184-186 |
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creator | ASANO, Yasutomi IIDA, Akira TOMIOKA, Kiyoshi |
description | The conjugate addition reaction of BHA alkenoates with butyl- and phenyllithiums in toluene at -78°C were catalyzed by a substoichiometric amount of chiral ligands 1 and 2 to give the corresponding 3-substituted alkanoates in good to modest ees. |
doi_str_mv | 10.1248/cpb.46.184 |
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Bull.</addtitle><description>The conjugate addition reaction of BHA alkenoates with butyl- and phenyllithiums in toluene at -78°C were catalyzed by a substoichiometric amount of chiral ligands 1 and 2 to give the corresponding 3-substituted alkanoates in good to modest ees.</description><subject>addition</subject><subject>Aliphatic compounds</subject><subject>catalyst</subject><subject>Chemistry</subject><subject>chiral ligand</subject><subject>Exact sciences and technology</subject><subject>Organic chemistry</subject><subject>organolithium</subject><subject>Preparations and properties</subject><issn>0009-2363</issn><issn>1347-5223</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNpFkEtPwzAQhC0EEuVx4RdEghNSyvqVx9GkoQkKiQQpEhywnNSGVqUtdjnw73EpgsvuYb6Z1Q5CZxiGmLDkql93QxYNccL20ABTFoecELqPBgCQhoRG9BAdOTcHIBxiOkAvbZEHWVHeiyqoyrGoR2EmWlE9PeejIK9F3ZbNQ17lWVs-erCpbydj0eaBGI1KL9VBcxM0997XVGVblJO7oG2C60J4b-O5E3Rg1MLp0999jCY3eZsVYdWMy0xUYc9jtglTgjtmcDdlmgKw1ABMWdInrOso8DhirI8iFWsSx2aadIYY_wlPteHMcAKYHqPzXe7arj4-tdvI-erTLv1JiVkEFAPn4KnLHdXblXNWG7m2s3dlvyQGue1P-v4ki6Tvz8MXv5HK9WphrFr2M_fnIARikmwvZzts7jbqVf_pym5m_UJvE3HKk5_U3fDh_-qbslIv6TcJW32v</recordid><startdate>19980101</startdate><enddate>19980101</enddate><creator>ASANO, Yasutomi</creator><creator>IIDA, Akira</creator><creator>TOMIOKA, Kiyoshi</creator><general>The Pharmaceutical Society of Japan</general><general>Maruzen</general><general>Japan Science and Technology Agency</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>H94</scope></search><sort><creationdate>19980101</creationdate><title>THE CHIRAL LIGAND-CATALYZED ENANTIOSELECTIVE CONJUGATE ADDITION OF ORGANOLITHIUM TO BHA ENOATE</title><author>ASANO, Yasutomi ; IIDA, Akira ; TOMIOKA, Kiyoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c574t-921b4f1bd4e30049f00d48c84bb3057644c66a7e277fd8bf2f36359ef54f52013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>addition</topic><topic>Aliphatic compounds</topic><topic>catalyst</topic><topic>Chemistry</topic><topic>chiral ligand</topic><topic>Exact sciences and technology</topic><topic>Organic chemistry</topic><topic>organolithium</topic><topic>Preparations and properties</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ASANO, Yasutomi</creatorcontrib><creatorcontrib>IIDA, Akira</creatorcontrib><creatorcontrib>TOMIOKA, Kiyoshi</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Chemical & pharmaceutical bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ASANO, Yasutomi</au><au>IIDA, Akira</au><au>TOMIOKA, Kiyoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>THE CHIRAL LIGAND-CATALYZED ENANTIOSELECTIVE CONJUGATE ADDITION OF ORGANOLITHIUM TO BHA ENOATE</atitle><jtitle>Chemical & pharmaceutical bulletin</jtitle><addtitle>Chem. Pharm. Bull.</addtitle><date>1998-01-01</date><risdate>1998</risdate><volume>46</volume><issue>1</issue><spage>184</spage><epage>186</epage><pages>184-186</pages><issn>0009-2363</issn><eissn>1347-5223</eissn><coden>CPBTAL</coden><abstract>The conjugate addition reaction of BHA alkenoates with butyl- and phenyllithiums in toluene at -78°C were catalyzed by a substoichiometric amount of chiral ligands 1 and 2 to give the corresponding 3-substituted alkanoates in good to modest ees.</abstract><cop>Tokyo</cop><pub>The Pharmaceutical Society of Japan</pub><doi>10.1248/cpb.46.184</doi><tpages>3</tpages><oa>free_for_read</oa></addata></record> |
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source | J-STAGE (Japan Science & Technology Information Aggregator, Electronic) Freely Available Titles - Japanese; EZB-FREE-00999 freely available EZB journals; Free Full-Text Journals in Chemistry |
subjects | addition Aliphatic compounds catalyst Chemistry chiral ligand Exact sciences and technology Organic chemistry organolithium Preparations and properties |
title | THE CHIRAL LIGAND-CATALYZED ENANTIOSELECTIVE CONJUGATE ADDITION OF ORGANOLITHIUM TO BHA ENOATE |
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