Metal-Catalyzed Enantioselective Allylation in Asymmetric Synthesis
Metal-catalyzed enantioselective allylation, which involves the substitution of allylic metal intermediates with a diverse range of different nucleophiles or SN2'-type allylic substitution, leads to the formation of C---H, ---C, ---O, ---N, ---S, and other bonds with very high levels of asymmet...
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Veröffentlicht in: | Angewandte Chemie (International ed.) 2008-01, Vol.47 (2), p.258-297 |
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description | Metal-catalyzed enantioselective allylation, which involves the substitution of allylic metal intermediates with a diverse range of different nucleophiles or SN2'-type allylic substitution, leads to the formation of C---H, ---C, ---O, ---N, ---S, and other bonds with very high levels of asymmetric induction. The reaction may tolerate a broad range of functional groups and has been applied successfully to the synthesis of many natural products and new chiral compounds. |
doi_str_mv | 10.1002/anie.200605113 |
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The reaction may tolerate a broad range of functional groups and has been applied successfully to the synthesis of many natural products and new chiral compounds.</description><subject>allylation</subject><subject>asymmetric catalysis</subject><subject>chiral ligands</subject><subject>natural products</subject><subject>regioselectivity</subject><issn>1433-7851</issn><issn>1521-3773</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqFkDtv2zAURokiRe2kXTs2mrLJ5UN8aDQM54E47uAaHQmKumqZUJIjymmVXx8aMpJsXS4viPN9uDgIfSV4RjCm303jYEYxFpgTwj6gKeGUpExKdhL3jLFUKk4m6DSE-8grhcUnNCEyF0oJPkWLO-iNTxcmzuEZymTZmKZ3bQAPtndPkMy9H7yJX03immQehrqGvnM22QxN_weCC5_Rx8r4AF-O7xnaXi5_Lq7T1Y-rm8V8ldrDbWlZQUFEwVhuC8mksCVXOc8qA8aajHCmGLY0k0ALKgRRVGXUAmeC4RyKkrAzdDH27rr2cQ-h17ULFrw3DbT7oCUmIpM4j-BsBG3XhtBBpXedq003aIL1QZs-aNOv2mLg27F5X9RQvuFHTxHIR-Cv8zD8p07P1zfL9-XpmHWhh3-vWdM9aBE9cP1rfaXFpcSrW7rSt5E_H_nKtNr87lzQ2w3FhGGsMpIJxV4AwESReA</recordid><startdate>20080101</startdate><enddate>20080101</enddate><creator>Lu, Zhan</creator><creator>Ma, Shengming</creator><general>Wiley-VCH Verlag</general><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><scope>FBQ</scope><scope>BSCLL</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20080101</creationdate><title>Metal-Catalyzed Enantioselective Allylation in Asymmetric Synthesis</title><author>Lu, Zhan ; Ma, Shengming</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5113-dfeb16b339cb7376cd58954faeaca4153830c247e2b266182842ce536309ebd13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>allylation</topic><topic>asymmetric catalysis</topic><topic>chiral ligands</topic><topic>natural products</topic><topic>regioselectivity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lu, Zhan</creatorcontrib><creatorcontrib>Ma, Shengming</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Angewandte Chemie (International ed.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lu, Zhan</au><au>Ma, Shengming</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metal-Catalyzed Enantioselective Allylation in Asymmetric Synthesis</atitle><jtitle>Angewandte Chemie (International ed.)</jtitle><addtitle>Angewandte Chemie International Edition</addtitle><date>2008-01-01</date><risdate>2008</risdate><volume>47</volume><issue>2</issue><spage>258</spage><epage>297</epage><pages>258-297</pages><issn>1433-7851</issn><eissn>1521-3773</eissn><abstract>Metal-catalyzed enantioselective allylation, which involves the substitution of allylic metal intermediates with a diverse range of different nucleophiles or SN2'-type allylic substitution, leads to the formation of C---H, ---C, ---O, ---N, ---S, and other bonds with very high levels of asymmetric induction. The reaction may tolerate a broad range of functional groups and has been applied successfully to the synthesis of many natural products and new chiral compounds.</abstract><cop>Weinheim</cop><pub>Wiley-VCH Verlag</pub><pmid>17968865</pmid><doi>10.1002/anie.200605113</doi><tpages>40</tpages><oa>free_for_read</oa></addata></record> |
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subjects | allylation asymmetric catalysis chiral ligands natural products regioselectivity |
title | Metal-Catalyzed Enantioselective Allylation in Asymmetric Synthesis |
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