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Article: Nickel-catalyzed three-component domino reactions of aryl grignard reagents, alkynes, and aryl halides producing tetrasubstituted alkenes

TitleNickel-catalyzed three-component domino reactions of aryl grignard reagents, alkynes, and aryl halides producing tetrasubstituted alkenes
Authors
Xue, FeiZhao, JinHor, T. S AndyHayashi, Tamio
Issue Date2015
Citation
Journal of the American Chemical Society, 2015, v. 137, n. 9, p. 3189-3192 How to Cite?
DOI: http://dx.doi.org/10.1021/ja513166w
Abstract© 2015 American Chemical Society. Three-component reaction of aryl Grignard reagents, alkynes, and aryl halides in the presence of 1 mol % of NiCl2 proceeded sequentially through carbomagnesiation of the alkyne followed by cross-coupling of the resulting alkenyl Grignard reagent with aryl halide to give tetrasubstituted alkenes in high yields.
Persistent Identifierhttp://hdl.handle.net/10722/219778
ISSN
0002-7863
2023 Impact Factor: 14.4
2023 SCImago Journal Rankings: 5.489
ISI Accession Number ID
WOS:000351187200010

 

DC FieldValueLanguage
dc.contributor.authorXue, Fei-
dc.contributor.authorZhao, Jin-
dc.contributor.authorHor, T. S Andy-
dc.contributor.authorHayashi, Tamio-
dc.date.accessioned2015-09-23T02:57:56Z-
dc.date.available2015-09-23T02:57:56Z-
dc.date.issued2015-
dc.identifier.citationJournal of the American Chemical Society, 2015, v. 137, n. 9, p. 3189-3192-
dc.identifier.issn0002-7863-
dc.identifier.urihttp://hdl.handle.net/10722/219778-
dc.description.abstract© 2015 American Chemical Society. Three-component reaction of aryl Grignard reagents, alkynes, and aryl halides in the presence of 1 mol % of NiCl2 proceeded sequentially through carbomagnesiation of the alkyne followed by cross-coupling of the resulting alkenyl Grignard reagent with aryl halide to give tetrasubstituted alkenes in high yields.-
dc.languageeng-
dc.relation.ispartofJournal of the American Chemical Society-
dc.titleNickel-catalyzed three-component domino reactions of aryl grignard reagents, alkynes, and aryl halides producing tetrasubstituted alkenes-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/ja513166w-
dc.identifier.pmid25714497-
dc.identifier.scopuseid_2-s2.0-84924706380-
dc.identifier.hkuros285699-
dc.identifier.volume137-
dc.identifier.issue9-
dc.identifier.spage3189-
dc.identifier.epage3192-
dc.identifier.eissn1520-5126-
dc.identifier.isiWOS:000351187200010-
dc.identifier.issnl0002-7863-

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