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Palladium-catalyzed enantioselective decarboxylative allylic alkylation of fully substituted N-acyl indole-derived enol carbonates

The first enantioselective palladium-catalyzed decarboxylative allylic alkylation of fully substituted N-acyl indole-derived enol carbonates forming acyclic all-carbon quaternary stereocenters is reported. Excellent yields up to 99% and enantioselectivities up to 98% ee are obtained through the use...

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Autores principales: Alexy, Eric J., Fulton, Tyler J., Zhang, Haiming, Stoltz, Brian M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6566452/
https://www.ncbi.nlm.nih.gov/pubmed/31360407
http://dx.doi.org/10.1039/c9sc01726g
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author Alexy, Eric J.
Fulton, Tyler J.
Zhang, Haiming
Stoltz, Brian M.
author_facet Alexy, Eric J.
Fulton, Tyler J.
Zhang, Haiming
Stoltz, Brian M.
author_sort Alexy, Eric J.
collection PubMed
description The first enantioselective palladium-catalyzed decarboxylative allylic alkylation of fully substituted N-acyl indole-derived enol carbonates forming acyclic all-carbon quaternary stereocenters is reported. Excellent yields up to 99% and enantioselectivities up to 98% ee are obtained through the use of a new electron-deficient phosphinoxazoline (PHOX) ligand. Control of substrate enolate geometry is crucial for high selectivity. The obtained α-quaternary N-acyl indoles are formal ester equivalents, and represent a useful handle for further synthetic transformations.
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spelling pubmed-65664522019-07-29 Palladium-catalyzed enantioselective decarboxylative allylic alkylation of fully substituted N-acyl indole-derived enol carbonates Alexy, Eric J. Fulton, Tyler J. Zhang, Haiming Stoltz, Brian M. Chem Sci Chemistry The first enantioselective palladium-catalyzed decarboxylative allylic alkylation of fully substituted N-acyl indole-derived enol carbonates forming acyclic all-carbon quaternary stereocenters is reported. Excellent yields up to 99% and enantioselectivities up to 98% ee are obtained through the use of a new electron-deficient phosphinoxazoline (PHOX) ligand. Control of substrate enolate geometry is crucial for high selectivity. The obtained α-quaternary N-acyl indoles are formal ester equivalents, and represent a useful handle for further synthetic transformations. Royal Society of Chemistry 2019-05-17 /pmc/articles/PMC6566452/ /pubmed/31360407 http://dx.doi.org/10.1039/c9sc01726g Text en This journal is © The Royal Society of Chemistry 2019 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0)
spellingShingle Chemistry
Alexy, Eric J.
Fulton, Tyler J.
Zhang, Haiming
Stoltz, Brian M.
Palladium-catalyzed enantioselective decarboxylative allylic alkylation of fully substituted N-acyl indole-derived enol carbonates
title Palladium-catalyzed enantioselective decarboxylative allylic alkylation of fully substituted N-acyl indole-derived enol carbonates
title_full Palladium-catalyzed enantioselective decarboxylative allylic alkylation of fully substituted N-acyl indole-derived enol carbonates
title_fullStr Palladium-catalyzed enantioselective decarboxylative allylic alkylation of fully substituted N-acyl indole-derived enol carbonates
title_full_unstemmed Palladium-catalyzed enantioselective decarboxylative allylic alkylation of fully substituted N-acyl indole-derived enol carbonates
title_short Palladium-catalyzed enantioselective decarboxylative allylic alkylation of fully substituted N-acyl indole-derived enol carbonates
title_sort palladium-catalyzed enantioselective decarboxylative allylic alkylation of fully substituted n-acyl indole-derived enol carbonates
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6566452/
https://www.ncbi.nlm.nih.gov/pubmed/31360407
http://dx.doi.org/10.1039/c9sc01726g
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