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Alkynes as Electrophilic or Nucleophilic Allylmetal Precursors in Transition‐Metal Catalysis
Diverse late transition metal catalysts convert terminal or internal alkynes into transient allylmetal species that display electrophilic or nucleophilic properties. Whereas classical methods for the generation of allylmetal species often form stoichiometric by‐products, the recent use of alkynes as...
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Published in: | Angewandte Chemie International Edition 2017-09, Vol.56 (38), p.11312-11325 |
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creator | Haydl, Alexander M. Breit, Bernhard Liang, Tao Krische, Michael J. |
description | Diverse late transition metal catalysts convert terminal or internal alkynes into transient allylmetal species that display electrophilic or nucleophilic properties. Whereas classical methods for the generation of allylmetal species often form stoichiometric by‐products, the recent use of alkynes as allylmetal precursors enables completely atom‐efficient catalytic processes to be carried out, including enantioselective transformations.
The best of both worlds: Diverse late transition metal catalysts can convert terminal or internal alkynes into transient allylmetal species that display electrophilic or nucleophilic properties. The use of alkynes as allylmetal precursors enables completely atom‐efficient catalytic processes to be carried out, including enantioselective transformations. |
doi_str_mv | 10.1002/anie.201704248 |
format | article |
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The best of both worlds: Diverse late transition metal catalysts can convert terminal or internal alkynes into transient allylmetal species that display electrophilic or nucleophilic properties. The use of alkynes as allylmetal precursors enables completely atom‐efficient catalytic processes to be carried out, including enantioselective transformations.</description><edition>International ed. in English</edition><identifier>ISSN: 1433-7851</identifier><identifier>EISSN: 1521-3773</identifier><identifier>DOI: 10.1002/anie.201704248</identifier><identifier>PMID: 28605083</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>Alkynes ; Alkynes - chemistry ; allylation ; Byproducts ; Catalysis ; Catalysts ; electrophiles ; Enantiomers ; Metals ; nucleophiles ; Organometallic Compounds - chemical synthesis ; Organometallic Compounds - chemistry ; Precursors ; Stereoisomerism ; Transition Elements - chemistry</subject><ispartof>Angewandte Chemie International Edition, 2017-09, Vol.56 (38), p.11312-11325</ispartof><rights>2017 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><rights>2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5348-f9cdaea2a7d0b66ef3185e84dea988e2e3f48f441b7d54db23559e3cb37f0e5a3</citedby><cites>FETCH-LOGICAL-c5348-f9cdaea2a7d0b66ef3185e84dea988e2e3f48f441b7d54db23559e3cb37f0e5a3</cites><orcidid>0000-0002-2514-3898</orcidid></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/28605083$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Haydl, Alexander M.</creatorcontrib><creatorcontrib>Breit, Bernhard</creatorcontrib><creatorcontrib>Liang, Tao</creatorcontrib><creatorcontrib>Krische, Michael J.</creatorcontrib><title>Alkynes as Electrophilic or Nucleophilic Allylmetal Precursors in Transition‐Metal Catalysis</title><title>Angewandte Chemie International Edition</title><addtitle>Angew Chem Int Ed Engl</addtitle><description>Diverse late transition metal catalysts convert terminal or internal alkynes into transient allylmetal species that display electrophilic or nucleophilic properties. Whereas classical methods for the generation of allylmetal species often form stoichiometric by‐products, the recent use of alkynes as allylmetal precursors enables completely atom‐efficient catalytic processes to be carried out, including enantioselective transformations.
The best of both worlds: Diverse late transition metal catalysts can convert terminal or internal alkynes into transient allylmetal species that display electrophilic or nucleophilic properties. 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The best of both worlds: Diverse late transition metal catalysts can convert terminal or internal alkynes into transient allylmetal species that display electrophilic or nucleophilic properties. The use of alkynes as allylmetal precursors enables completely atom‐efficient catalytic processes to be carried out, including enantioselective transformations.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>28605083</pmid><doi>10.1002/anie.201704248</doi><tpages>14</tpages><edition>International ed. in English</edition><orcidid>https://orcid.org/0000-0002-2514-3898</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Alkynes Alkynes - chemistry allylation Byproducts Catalysis Catalysts electrophiles Enantiomers Metals nucleophiles Organometallic Compounds - chemical synthesis Organometallic Compounds - chemistry Precursors Stereoisomerism Transition Elements - chemistry |
title | Alkynes as Electrophilic or Nucleophilic Allylmetal Precursors in Transition‐Metal Catalysis |
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