Cargando…

Enantioselective CuH-Catalyzed Hydroallylation of Vinylarenes

[Image: see text] The enantioselective, intermolecular hydroallylation of vinylarenes employing allylic phosphate electrophiles has been achieved through a copper hydride catalyzed process. The protocol described herein can be applied to a diverse set of vinylarene substrates and allows for the inst...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Yi-Ming, Buchwald, Stephen L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2016
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4851114/
https://www.ncbi.nlm.nih.gov/pubmed/27042864
http://dx.doi.org/10.1021/jacs.6b02527
_version_ 1782429778139152384
author Wang, Yi-Ming
Buchwald, Stephen L.
author_facet Wang, Yi-Ming
Buchwald, Stephen L.
author_sort Wang, Yi-Ming
collection PubMed
description [Image: see text] The enantioselective, intermolecular hydroallylation of vinylarenes employing allylic phosphate electrophiles has been achieved through a copper hydride catalyzed process. The protocol described herein can be applied to a diverse set of vinylarene substrates and allows for the installation of the parent allyl group as well as a range of 2-substituted allylic fragments.
format Online
Article
Text
id pubmed-4851114
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher American Chemical Society
record_format MEDLINE/PubMed
spelling pubmed-48511142017-04-04 Enantioselective CuH-Catalyzed Hydroallylation of Vinylarenes Wang, Yi-Ming Buchwald, Stephen L. J Am Chem Soc [Image: see text] The enantioselective, intermolecular hydroallylation of vinylarenes employing allylic phosphate electrophiles has been achieved through a copper hydride catalyzed process. The protocol described herein can be applied to a diverse set of vinylarene substrates and allows for the installation of the parent allyl group as well as a range of 2-substituted allylic fragments. American Chemical Society 2016-04-04 2016-04-20 /pmc/articles/PMC4851114/ /pubmed/27042864 http://dx.doi.org/10.1021/jacs.6b02527 Text en Copyright © 2016 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Wang, Yi-Ming
Buchwald, Stephen L.
Enantioselective CuH-Catalyzed Hydroallylation of Vinylarenes
title Enantioselective CuH-Catalyzed Hydroallylation of Vinylarenes
title_full Enantioselective CuH-Catalyzed Hydroallylation of Vinylarenes
title_fullStr Enantioselective CuH-Catalyzed Hydroallylation of Vinylarenes
title_full_unstemmed Enantioselective CuH-Catalyzed Hydroallylation of Vinylarenes
title_short Enantioselective CuH-Catalyzed Hydroallylation of Vinylarenes
title_sort enantioselective cuh-catalyzed hydroallylation of vinylarenes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4851114/
https://www.ncbi.nlm.nih.gov/pubmed/27042864
http://dx.doi.org/10.1021/jacs.6b02527
work_keys_str_mv AT wangyiming enantioselectivecuhcatalyzedhydroallylationofvinylarenes
AT buchwaldstephenl enantioselectivecuhcatalyzedhydroallylationofvinylarenes