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Cobalt-catalyzed directed C–H alkenylation of pivalophenone N–H imine with alkenyl phosphates
A cobalt–N-heterocyclic carbene (NHC) catalyst efficiently promotes an ortho C–H alkenylation reaction of pivalophenone N–H imine with an alkenyl phosphate. The reaction tolerates various substituted pivalophenone N–H imines as well as cyclic and acyclic alkenyl phosphates.
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5905286/ https://www.ncbi.nlm.nih.gov/pubmed/29719569 http://dx.doi.org/10.3762/bjoc.14.60 |
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author | Xu, Wengang Yoshikai, Naohiko |
author_facet | Xu, Wengang Yoshikai, Naohiko |
author_sort | Xu, Wengang |
collection | PubMed |
description | A cobalt–N-heterocyclic carbene (NHC) catalyst efficiently promotes an ortho C–H alkenylation reaction of pivalophenone N–H imine with an alkenyl phosphate. The reaction tolerates various substituted pivalophenone N–H imines as well as cyclic and acyclic alkenyl phosphates. |
format | Online Article Text |
id | pubmed-5905286 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-59052862018-05-01 Cobalt-catalyzed directed C–H alkenylation of pivalophenone N–H imine with alkenyl phosphates Xu, Wengang Yoshikai, Naohiko Beilstein J Org Chem Full Research Paper A cobalt–N-heterocyclic carbene (NHC) catalyst efficiently promotes an ortho C–H alkenylation reaction of pivalophenone N–H imine with an alkenyl phosphate. The reaction tolerates various substituted pivalophenone N–H imines as well as cyclic and acyclic alkenyl phosphates. Beilstein-Institut 2018-03-28 /pmc/articles/PMC5905286/ /pubmed/29719569 http://dx.doi.org/10.3762/bjoc.14.60 Text en Copyright © 2018, Xu and Yoshikai https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Full Research Paper Xu, Wengang Yoshikai, Naohiko Cobalt-catalyzed directed C–H alkenylation of pivalophenone N–H imine with alkenyl phosphates |
title | Cobalt-catalyzed directed C–H alkenylation of pivalophenone N–H imine with alkenyl phosphates |
title_full | Cobalt-catalyzed directed C–H alkenylation of pivalophenone N–H imine with alkenyl phosphates |
title_fullStr | Cobalt-catalyzed directed C–H alkenylation of pivalophenone N–H imine with alkenyl phosphates |
title_full_unstemmed | Cobalt-catalyzed directed C–H alkenylation of pivalophenone N–H imine with alkenyl phosphates |
title_short | Cobalt-catalyzed directed C–H alkenylation of pivalophenone N–H imine with alkenyl phosphates |
title_sort | cobalt-catalyzed directed c–h alkenylation of pivalophenone n–h imine with alkenyl phosphates |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5905286/ https://www.ncbi.nlm.nih.gov/pubmed/29719569 http://dx.doi.org/10.3762/bjoc.14.60 |
work_keys_str_mv | AT xuwengang cobaltcatalyzeddirectedchalkenylationofpivalophenonenhiminewithalkenylphosphates AT yoshikainaohiko cobaltcatalyzeddirectedchalkenylationofpivalophenonenhiminewithalkenylphosphates |