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Nonenzymatic enantioselective synthesis of all-carbon quaternary centers through desymmetrization
[Display omitted] The asymmetric desymmetrization of meso or prochiral compounds containing an all-carbon quaternary center is an attractive alternative to classical synthetic approaches aimed at the asymmetric formation of a new C–C bond. This review focuses on nonenzymatic desymmetrizations that u...
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Published in: | Tetrahedron letters 2015-11, Vol.56 (47), p.6523-6535 |
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container_title | Tetrahedron letters |
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creator | Petersen, Kimberly S. |
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The asymmetric desymmetrization of meso or prochiral compounds containing an all-carbon quaternary center is an attractive alternative to classical synthetic approaches aimed at the asymmetric formation of a new C–C bond. This review focuses on nonenzymatic desymmetrizations that utilize transition metal catalysts or organocatalysts to distinguish between enantiotopic groups to generate enantioenriched compounds containing all-carbon quaternary stereocenters. |
doi_str_mv | 10.1016/j.tetlet.2015.09.134 |
format | article |
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The asymmetric desymmetrization of meso or prochiral compounds containing an all-carbon quaternary center is an attractive alternative to classical synthetic approaches aimed at the asymmetric formation of a new C–C bond. This review focuses on nonenzymatic desymmetrizations that utilize transition metal catalysts or organocatalysts to distinguish between enantiotopic groups to generate enantioenriched compounds containing all-carbon quaternary stereocenters.</description><identifier>ISSN: 0040-4039</identifier><identifier>EISSN: 1873-3581</identifier><identifier>DOI: 10.1016/j.tetlet.2015.09.134</identifier><identifier>PMID: 26834295</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>All-carbon quaternary center ; Asymmetric ; Desymmetrization ; Organocatalysis ; Transition-metal catalysis</subject><ispartof>Tetrahedron letters, 2015-11, Vol.56 (47), p.6523-6535</ispartof><rights>2015 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c529t-8c30dac197faaf4836d49dc49ac16a130713d5c4702dcfd42902fa1dd2dc72c13</citedby><cites>FETCH-LOGICAL-c529t-8c30dac197faaf4836d49dc49ac16a130713d5c4702dcfd42902fa1dd2dc72c13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26834295$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Petersen, Kimberly S.</creatorcontrib><title>Nonenzymatic enantioselective synthesis of all-carbon quaternary centers through desymmetrization</title><title>Tetrahedron letters</title><addtitle>Tetrahedron Lett</addtitle><description>[Display omitted]
The asymmetric desymmetrization of meso or prochiral compounds containing an all-carbon quaternary center is an attractive alternative to classical synthetic approaches aimed at the asymmetric formation of a new C–C bond. This review focuses on nonenzymatic desymmetrizations that utilize transition metal catalysts or organocatalysts to distinguish between enantiotopic groups to generate enantioenriched compounds containing all-carbon quaternary stereocenters.</description><subject>All-carbon quaternary center</subject><subject>Asymmetric</subject><subject>Desymmetrization</subject><subject>Organocatalysis</subject><subject>Transition-metal catalysis</subject><issn>0040-4039</issn><issn>1873-3581</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNp9kU1P3DAQhq0KVLbAP6hQjlySjmPnwxekCkFbCbUXOFtee8J6ldhgOystvx5vF7btpb6MP2beeccPIZ8pVBRo-2VdJUwjpqoG2lQgKsr4B7KgfcdK1vT0iCwAOJQcmDghn2JcQ15tDx_JSd32jNeiWRD10zt0L9tJJasLdMol6yOOqJPdYBG3Lq0w2lj4oVDjWGoVlt4Vz7NKGJwK20Kjy9tYpFXw8-OqMBi304Qp2Jes6d0ZOR7UGPH8LZ6Sh9ub--vv5d2vbz-uv96VuqlFKnvNwChNRTcoNfCetYYLo7nId62iDDrKTKN5B7XRg8nuoR4UNSYfu1pTdkqu9rpP83JCs7MV1Cifgp2yTemVlf--OLuSj34jecdAwE7g8k0g-OcZY5KTjRrHUTn0c5S0r9u2EfR3Kt-n6uBjDDgc2lCQOzpyLfd05I6OBCEznVx28bfFQ9E7jj8zYP6ojcUgo7boNBobMhFpvP1_h1cdQae1</recordid><startdate>20151125</startdate><enddate>20151125</enddate><creator>Petersen, Kimberly S.</creator><general>Elsevier Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20151125</creationdate><title>Nonenzymatic enantioselective synthesis of all-carbon quaternary centers through desymmetrization</title><author>Petersen, Kimberly S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c529t-8c30dac197faaf4836d49dc49ac16a130713d5c4702dcfd42902fa1dd2dc72c13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>All-carbon quaternary center</topic><topic>Asymmetric</topic><topic>Desymmetrization</topic><topic>Organocatalysis</topic><topic>Transition-metal catalysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Petersen, Kimberly S.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Tetrahedron letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Petersen, Kimberly S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nonenzymatic enantioselective synthesis of all-carbon quaternary centers through desymmetrization</atitle><jtitle>Tetrahedron letters</jtitle><addtitle>Tetrahedron Lett</addtitle><date>2015-11-25</date><risdate>2015</risdate><volume>56</volume><issue>47</issue><spage>6523</spage><epage>6535</epage><pages>6523-6535</pages><issn>0040-4039</issn><eissn>1873-3581</eissn><abstract>[Display omitted]
The asymmetric desymmetrization of meso or prochiral compounds containing an all-carbon quaternary center is an attractive alternative to classical synthetic approaches aimed at the asymmetric formation of a new C–C bond. This review focuses on nonenzymatic desymmetrizations that utilize transition metal catalysts or organocatalysts to distinguish between enantiotopic groups to generate enantioenriched compounds containing all-carbon quaternary stereocenters.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>26834295</pmid><doi>10.1016/j.tetlet.2015.09.134</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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source | ScienceDirect Journals |
subjects | All-carbon quaternary center Asymmetric Desymmetrization Organocatalysis Transition-metal catalysis |
title | Nonenzymatic enantioselective synthesis of all-carbon quaternary centers through desymmetrization |
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