Decarboxylation as the Key Step in C−C Bond‐Forming Reactions
C−C bond forming reactions incarnate the core of organic synthesis because of their fundamental applications to molecular diversity and complexity. In recent years, use of carboxylic acid as one of the coupling partners in place of conventional organometallic reagents has seen an upsurge due to its...
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Veröffentlicht in: | Chemistry : a European journal 2017-06, Vol.23 (31), p.7382-7401 |
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creator | Patra, Tuhin Maiti, Debabrata |
description | C−C bond forming reactions incarnate the core of organic synthesis because of their fundamental applications to molecular diversity and complexity. In recent years, use of carboxylic acid as one of the coupling partners in place of conventional organometallic reagents has seen an upsurge due to its potency to generate similar organometallic intermediates after decarboxylation. This Review provides an overview on the most recent progress in the field of C−C bond formation involving decarboxylation as a key step. Different important developments, which are not included in earlier Reviews in this area, have been summarized with representative examples and discussions on their reaction mechanisms.
C here: This Review article covers the recent and important developments in the rapidly growing field of decarboxylative C−C bond formation. |
doi_str_mv | 10.1002/chem.201604496 |
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C here: This Review article covers the recent and important developments in the rapidly growing field of decarboxylative C−C bond formation.</description><subject>Carboxylic acids</subject><subject>Chemistry</subject><subject>Coupling (molecular)</subject><subject>C−C coupling</subject><subject>Decarboxylation</subject><subject>Intermediates</subject><subject>Reaction mechanisms</subject><subject>Reagents</subject><subject>Reviews</subject><subject>synthetic methods</subject><issn>0947-6539</issn><issn>1521-3765</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqFkDtPwzAURi0EoqWwMiJLLCwpficeS2gpogiJx2w5jkNT5VHiVJCNkRHxE_tLSNVSJBamu5zv6OoAcIxRHyNEzs3U5n2CsECMSbEDupgT7FFf8F3QRZL5nuBUdsCBczOEkBSU7oMO8QMufSy7YHBpja6i8q3JdJ2WBdQO1lMLb2wDH2o7h2kBw-XHVwgvyiJevn-OyipPi2d4b7VZDdwh2Et05uzR5vbA02j4GI69yd3VdTiYeIYzIbwgsZxGVKBESi5oEsiE4ZgEmAY69rmPI4MooVz7iUaM2phxFhgex5IYJKKE9sDZ2juvypeFdbXKU2dslunClguncMBwgIgkrEVP_6CzclEV7XcKS8Qwa9PxluqvKVOVzlU2UfMqzXXVKIzUKq5axVXbuO3gZKNdRLmNt_hPzRaQa-A1zWzzj06F4-Htr_wb7PWFNA</recordid><startdate>20170601</startdate><enddate>20170601</enddate><creator>Patra, Tuhin</creator><creator>Maiti, Debabrata</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>20170601</creationdate><title>Decarboxylation as the Key Step in C−C Bond‐Forming Reactions</title><author>Patra, Tuhin ; Maiti, Debabrata</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5466-8fe53b360f99563f89f41d28138ad7571bc03235a7fa043ed4548c5dd92c06bf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Carboxylic acids</topic><topic>Chemistry</topic><topic>Coupling (molecular)</topic><topic>C−C coupling</topic><topic>Decarboxylation</topic><topic>Intermediates</topic><topic>Reaction mechanisms</topic><topic>Reagents</topic><topic>Reviews</topic><topic>synthetic methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Patra, Tuhin</creatorcontrib><creatorcontrib>Maiti, Debabrata</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Chemistry : a European journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Patra, Tuhin</au><au>Maiti, Debabrata</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Decarboxylation as the Key Step in C−C Bond‐Forming Reactions</atitle><jtitle>Chemistry : a European journal</jtitle><addtitle>Chemistry</addtitle><date>2017-06-01</date><risdate>2017</risdate><volume>23</volume><issue>31</issue><spage>7382</spage><epage>7401</epage><pages>7382-7401</pages><issn>0947-6539</issn><eissn>1521-3765</eissn><abstract>C−C bond forming reactions incarnate the core of organic synthesis because of their fundamental applications to molecular diversity and complexity. In recent years, use of carboxylic acid as one of the coupling partners in place of conventional organometallic reagents has seen an upsurge due to its potency to generate similar organometallic intermediates after decarboxylation. This Review provides an overview on the most recent progress in the field of C−C bond formation involving decarboxylation as a key step. Different important developments, which are not included in earlier Reviews in this area, have been summarized with representative examples and discussions on their reaction mechanisms.
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subjects | Carboxylic acids Chemistry Coupling (molecular) C−C coupling Decarboxylation Intermediates Reaction mechanisms Reagents Reviews synthetic methods |
title | Decarboxylation as the Key Step in C−C Bond‐Forming Reactions |
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