Cargando…

Enantioselective Nickel‐Catalyzed Intramolecular Allylic Alkenylations Enabled by Reversible Alkenylnickel E/Z Isomerization

Enantioselective nickel‐catalyzed arylative cyclizations of substrates containing a Z‐allylic phosphate tethered to an alkyne are described. These reactions give multisubstituted chiral aza‐ and carbocycles, and are initiated by the addition of an arylboronic acid to the alkyne, followed by cyclizat...

Descripción completa

Detalles Bibliográficos
Autores principales: Yap, Connor, Lenagh‐Snow, Gabriel M. J., Karad, Somnath Narayan, Lewis, William, Diorazio, Louis J., Lam, Hon Wai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5499723/
https://www.ncbi.nlm.nih.gov/pubmed/28544752
http://dx.doi.org/10.1002/anie.201703380
_version_ 1783248516293853184
author Yap, Connor
Lenagh‐Snow, Gabriel M. J.
Karad, Somnath Narayan
Lewis, William
Diorazio, Louis J.
Lam, Hon Wai
author_facet Yap, Connor
Lenagh‐Snow, Gabriel M. J.
Karad, Somnath Narayan
Lewis, William
Diorazio, Louis J.
Lam, Hon Wai
author_sort Yap, Connor
collection PubMed
description Enantioselective nickel‐catalyzed arylative cyclizations of substrates containing a Z‐allylic phosphate tethered to an alkyne are described. These reactions give multisubstituted chiral aza‐ and carbocycles, and are initiated by the addition of an arylboronic acid to the alkyne, followed by cyclization of the resulting alkenylnickel species onto the allylic phosphate. The reversible E/Z isomerization of the alkenylnickel species is essential for the success of the reactions.
format Online
Article
Text
id pubmed-5499723
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-54997232017-07-21 Enantioselective Nickel‐Catalyzed Intramolecular Allylic Alkenylations Enabled by Reversible Alkenylnickel E/Z Isomerization Yap, Connor Lenagh‐Snow, Gabriel M. J. Karad, Somnath Narayan Lewis, William Diorazio, Louis J. Lam, Hon Wai Angew Chem Int Ed Engl Communications Enantioselective nickel‐catalyzed arylative cyclizations of substrates containing a Z‐allylic phosphate tethered to an alkyne are described. These reactions give multisubstituted chiral aza‐ and carbocycles, and are initiated by the addition of an arylboronic acid to the alkyne, followed by cyclization of the resulting alkenylnickel species onto the allylic phosphate. The reversible E/Z isomerization of the alkenylnickel species is essential for the success of the reactions. John Wiley and Sons Inc. 2017-06-12 2017-07-03 /pmc/articles/PMC5499723/ /pubmed/28544752 http://dx.doi.org/10.1002/anie.201703380 Text en © 2017 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution (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
Yap, Connor
Lenagh‐Snow, Gabriel M. J.
Karad, Somnath Narayan
Lewis, William
Diorazio, Louis J.
Lam, Hon Wai
Enantioselective Nickel‐Catalyzed Intramolecular Allylic Alkenylations Enabled by Reversible Alkenylnickel E/Z Isomerization
title Enantioselective Nickel‐Catalyzed Intramolecular Allylic Alkenylations Enabled by Reversible Alkenylnickel E/Z Isomerization
title_full Enantioselective Nickel‐Catalyzed Intramolecular Allylic Alkenylations Enabled by Reversible Alkenylnickel E/Z Isomerization
title_fullStr Enantioselective Nickel‐Catalyzed Intramolecular Allylic Alkenylations Enabled by Reversible Alkenylnickel E/Z Isomerization
title_full_unstemmed Enantioselective Nickel‐Catalyzed Intramolecular Allylic Alkenylations Enabled by Reversible Alkenylnickel E/Z Isomerization
title_short Enantioselective Nickel‐Catalyzed Intramolecular Allylic Alkenylations Enabled by Reversible Alkenylnickel E/Z Isomerization
title_sort enantioselective nickel‐catalyzed intramolecular allylic alkenylations enabled by reversible alkenylnickel e/z isomerization
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5499723/
https://www.ncbi.nlm.nih.gov/pubmed/28544752
http://dx.doi.org/10.1002/anie.201703380
work_keys_str_mv AT yapconnor enantioselectivenickelcatalyzedintramolecularallylicalkenylationsenabledbyreversiblealkenylnickelezisomerization
AT lenaghsnowgabrielmj enantioselectivenickelcatalyzedintramolecularallylicalkenylationsenabledbyreversiblealkenylnickelezisomerization
AT karadsomnathnarayan enantioselectivenickelcatalyzedintramolecularallylicalkenylationsenabledbyreversiblealkenylnickelezisomerization
AT lewiswilliam enantioselectivenickelcatalyzedintramolecularallylicalkenylationsenabledbyreversiblealkenylnickelezisomerization
AT dioraziolouisj enantioselectivenickelcatalyzedintramolecularallylicalkenylationsenabledbyreversiblealkenylnickelezisomerization
AT lamhonwai enantioselectivenickelcatalyzedintramolecularallylicalkenylationsenabledbyreversiblealkenylnickelezisomerization