Cargando…
Iridium‐Catalyzed α‐Selective Arylation of Styrenes by Dual C−H Functionalization
An Ir(I)‐system modified with a ferrocene derived bisphosphine ligand promotes α‐selective arylation of styrenes by dual C−H functionalization. These studies offer a regioisomeric alternative to the Pd‐catalyzed Fujiwara–Moritani reaction.
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391973/ https://www.ncbi.nlm.nih.gov/pubmed/30171652 http://dx.doi.org/10.1002/anie.201808299 |
_version_ | 1783398402920284160 |
---|---|
author | Cooper, Phillippa Crisenza, Giacomo E. M. Feron, Lyman J. Bower, John F. |
author_facet | Cooper, Phillippa Crisenza, Giacomo E. M. Feron, Lyman J. Bower, John F. |
author_sort | Cooper, Phillippa |
collection | PubMed |
description | An Ir(I)‐system modified with a ferrocene derived bisphosphine ligand promotes α‐selective arylation of styrenes by dual C−H functionalization. These studies offer a regioisomeric alternative to the Pd‐catalyzed Fujiwara–Moritani reaction. |
format | Online Article Text |
id | pubmed-6391973 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63919732019-03-07 Iridium‐Catalyzed α‐Selective Arylation of Styrenes by Dual C−H Functionalization Cooper, Phillippa Crisenza, Giacomo E. M. Feron, Lyman J. Bower, John F. Angew Chem Int Ed Engl Communications An Ir(I)‐system modified with a ferrocene derived bisphosphine ligand promotes α‐selective arylation of styrenes by dual C−H functionalization. These studies offer a regioisomeric alternative to the Pd‐catalyzed Fujiwara–Moritani reaction. John Wiley and Sons Inc. 2018-09-26 2018-10-22 /pmc/articles/PMC6391973/ /pubmed/30171652 http://dx.doi.org/10.1002/anie.201808299 Text en © 2018 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Communications Cooper, Phillippa Crisenza, Giacomo E. M. Feron, Lyman J. Bower, John F. Iridium‐Catalyzed α‐Selective Arylation of Styrenes by Dual C−H Functionalization |
title | Iridium‐Catalyzed α‐Selective Arylation of Styrenes by Dual C−H Functionalization |
title_full | Iridium‐Catalyzed α‐Selective Arylation of Styrenes by Dual C−H Functionalization |
title_fullStr | Iridium‐Catalyzed α‐Selective Arylation of Styrenes by Dual C−H Functionalization |
title_full_unstemmed | Iridium‐Catalyzed α‐Selective Arylation of Styrenes by Dual C−H Functionalization |
title_short | Iridium‐Catalyzed α‐Selective Arylation of Styrenes by Dual C−H Functionalization |
title_sort | iridium‐catalyzed α‐selective arylation of styrenes by dual c−h functionalization |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391973/ https://www.ncbi.nlm.nih.gov/pubmed/30171652 http://dx.doi.org/10.1002/anie.201808299 |
work_keys_str_mv | AT cooperphillippa iridiumcatalyzedaselectivearylationofstyrenesbydualchfunctionalization AT crisenzagiacomoem iridiumcatalyzedaselectivearylationofstyrenesbydualchfunctionalization AT feronlymanj iridiumcatalyzedaselectivearylationofstyrenesbydualchfunctionalization AT bowerjohnf iridiumcatalyzedaselectivearylationofstyrenesbydualchfunctionalization |