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Decarboxylative Benzylation of Aryl and Alkenyl Boronic Esters
The copper‐catalyzed decarboxylative benzylation of aryl and alkenyl boronic esters with electron‐deficient aryl acetates is reported. The oxidative coupling proceeds under mild, aerobic conditions and tolerates a host of potentially reactive electrophilic functional groups that would be problematic...
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Published in: | Angewandte Chemie 2018-04, Vol.130 (17), p.4702-4706 |
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container_end_page | 4706 |
container_issue | 17 |
container_start_page | 4702 |
container_title | Angewandte Chemie |
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creator | Moon, Patrick J. Fahandej‐Sadi, Anis Qian, Wenyu Lundgren, Rylan J. |
description | The copper‐catalyzed decarboxylative benzylation of aryl and alkenyl boronic esters with electron‐deficient aryl acetates is reported. The oxidative coupling proceeds under mild, aerobic conditions and tolerates a host of potentially reactive electrophilic functional groups that would be problematic with traditional benzylation methods (aryl iodides and bromides, protic heteroatoms, aldehydes, Michael acceptors). A reaction pathway in which a benzylic nucleophile is generated by aryl acetate decarboxylation and in turn is intercepted by the catalyst to form diarylmethane products is supported by mechanistic studies.
An der Luft: Die Kupfer‐katalysierte decarboxylierende Benzylierung von Aryl‐ und Alkenylboronsäureestern mit elektronenarmen Arylacetaten gelingt unter milden aeroben Bedingungen. Viele reaktive, elektrophile funktionelle Gruppen werden toleriert, deren Einsatz in gewöhnlichen Benzylierungen problematisch ist. |
doi_str_mv | 10.1002/ange.201800829 |
format | article |
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An der Luft: Die Kupfer‐katalysierte decarboxylierende Benzylierung von Aryl‐ und Alkenylboronsäureestern mit elektronenarmen Arylacetaten gelingt unter milden aeroben Bedingungen. Viele reaktive, elektrophile funktionelle Gruppen werden toleriert, deren Einsatz in gewöhnlichen Benzylierungen problematisch ist.</description><identifier>ISSN: 0044-8249</identifier><identifier>EISSN: 1521-3757</identifier><identifier>DOI: 10.1002/ange.201800829</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>Acetates ; Acetic acid ; Aerobe Katalyse ; Aerobic conditions ; Aldehydes ; Aromatic compounds ; Bor ; Bromides ; Chemistry ; Decarboxylation ; Decarboxylierungen ; Esters ; Functional groups ; Iodides ; Kreuzkupplungen ; Kupfer</subject><ispartof>Angewandte Chemie, 2018-04, Vol.130 (17), p.4702-4706</ispartof><rights>2018 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1629-991e28969003140636d0afc80473aead94f8a352b2a08a0dcb9a9f82336bde9e3</citedby><cites>FETCH-LOGICAL-c1629-991e28969003140636d0afc80473aead94f8a352b2a08a0dcb9a9f82336bde9e3</cites><orcidid>0000-0003-0555-1621 ; 0000-0002-7760-6946</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Moon, Patrick J.</creatorcontrib><creatorcontrib>Fahandej‐Sadi, Anis</creatorcontrib><creatorcontrib>Qian, Wenyu</creatorcontrib><creatorcontrib>Lundgren, Rylan J.</creatorcontrib><title>Decarboxylative Benzylation of Aryl and Alkenyl Boronic Esters</title><title>Angewandte Chemie</title><description>The copper‐catalyzed decarboxylative benzylation of aryl and alkenyl boronic esters with electron‐deficient aryl acetates is reported. The oxidative coupling proceeds under mild, aerobic conditions and tolerates a host of potentially reactive electrophilic functional groups that would be problematic with traditional benzylation methods (aryl iodides and bromides, protic heteroatoms, aldehydes, Michael acceptors). A reaction pathway in which a benzylic nucleophile is generated by aryl acetate decarboxylation and in turn is intercepted by the catalyst to form diarylmethane products is supported by mechanistic studies.
An der Luft: Die Kupfer‐katalysierte decarboxylierende Benzylierung von Aryl‐ und Alkenylboronsäureestern mit elektronenarmen Arylacetaten gelingt unter milden aeroben Bedingungen. Viele reaktive, elektrophile funktionelle Gruppen werden toleriert, deren Einsatz in gewöhnlichen Benzylierungen problematisch ist.</description><subject>Acetates</subject><subject>Acetic acid</subject><subject>Aerobe Katalyse</subject><subject>Aerobic conditions</subject><subject>Aldehydes</subject><subject>Aromatic compounds</subject><subject>Bor</subject><subject>Bromides</subject><subject>Chemistry</subject><subject>Decarboxylation</subject><subject>Decarboxylierungen</subject><subject>Esters</subject><subject>Functional groups</subject><subject>Iodides</subject><subject>Kreuzkupplungen</subject><subject>Kupfer</subject><issn>0044-8249</issn><issn>1521-3757</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNqFkDtPwzAUhS0EEqWwMkdiTrm-zsNekNJSClIFC8yWk9yglGAXuzzCryelCEame4bvO1c6jJ1ymHAAPDf2kSYIXAJIVHtsxFPkscjTfJ-NAJIklpioQ3YUwgoAMszViF1cUmV86T76zmzaN4qmZD-_s7ORa6LC911kbB0V3RPZIU-dd7atonnYkA_H7KAxXaCTnztmD1fz-9l1vLxb3MyKZVzxDFWsFCeUKlMAgieQiawG01QSklwYMrVKGmlEiiUakAbqqlRGNRKFyMqaFIkxO9v1rr17eaWw0Sv36u3wUiNgKjimqRyoyY6qvAvBU6PXvn02vtcc9HYjvd1I_240CGonvLcd9f_QurhdzP_cL949aeM</recordid><startdate>20180416</startdate><enddate>20180416</enddate><creator>Moon, Patrick J.</creator><creator>Fahandej‐Sadi, Anis</creator><creator>Qian, Wenyu</creator><creator>Lundgren, Rylan J.</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><orcidid>https://orcid.org/0000-0003-0555-1621</orcidid><orcidid>https://orcid.org/0000-0002-7760-6946</orcidid></search><sort><creationdate>20180416</creationdate><title>Decarboxylative Benzylation of Aryl and Alkenyl Boronic Esters</title><author>Moon, Patrick J. ; Fahandej‐Sadi, Anis ; Qian, Wenyu ; Lundgren, Rylan J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1629-991e28969003140636d0afc80473aead94f8a352b2a08a0dcb9a9f82336bde9e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Acetates</topic><topic>Acetic acid</topic><topic>Aerobe Katalyse</topic><topic>Aerobic conditions</topic><topic>Aldehydes</topic><topic>Aromatic compounds</topic><topic>Bor</topic><topic>Bromides</topic><topic>Chemistry</topic><topic>Decarboxylation</topic><topic>Decarboxylierungen</topic><topic>Esters</topic><topic>Functional groups</topic><topic>Iodides</topic><topic>Kreuzkupplungen</topic><topic>Kupfer</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Moon, Patrick J.</creatorcontrib><creatorcontrib>Fahandej‐Sadi, Anis</creatorcontrib><creatorcontrib>Qian, Wenyu</creatorcontrib><creatorcontrib>Lundgren, Rylan J.</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Angewandte Chemie</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Moon, Patrick J.</au><au>Fahandej‐Sadi, Anis</au><au>Qian, Wenyu</au><au>Lundgren, Rylan J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Decarboxylative Benzylation of Aryl and Alkenyl Boronic Esters</atitle><jtitle>Angewandte Chemie</jtitle><date>2018-04-16</date><risdate>2018</risdate><volume>130</volume><issue>17</issue><spage>4702</spage><epage>4706</epage><pages>4702-4706</pages><issn>0044-8249</issn><eissn>1521-3757</eissn><abstract>The copper‐catalyzed decarboxylative benzylation of aryl and alkenyl boronic esters with electron‐deficient aryl acetates is reported. The oxidative coupling proceeds under mild, aerobic conditions and tolerates a host of potentially reactive electrophilic functional groups that would be problematic with traditional benzylation methods (aryl iodides and bromides, protic heteroatoms, aldehydes, Michael acceptors). A reaction pathway in which a benzylic nucleophile is generated by aryl acetate decarboxylation and in turn is intercepted by the catalyst to form diarylmethane products is supported by mechanistic studies.
An der Luft: Die Kupfer‐katalysierte decarboxylierende Benzylierung von Aryl‐ und Alkenylboronsäureestern mit elektronenarmen Arylacetaten gelingt unter milden aeroben Bedingungen. Viele reaktive, elektrophile funktionelle Gruppen werden toleriert, deren Einsatz in gewöhnlichen Benzylierungen problematisch ist.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/ange.201800829</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0003-0555-1621</orcidid><orcidid>https://orcid.org/0000-0002-7760-6946</orcidid></addata></record> |
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subjects | Acetates Acetic acid Aerobe Katalyse Aerobic conditions Aldehydes Aromatic compounds Bor Bromides Chemistry Decarboxylation Decarboxylierungen Esters Functional groups Iodides Kreuzkupplungen Kupfer |
title | Decarboxylative Benzylation of Aryl and Alkenyl Boronic Esters |
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