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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2019
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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. |
format | Online Article Text |
id | pubmed-6566452 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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
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title_full | Palladium-catalyzed enantioselective decarboxylative allylic alkylation of fully substituted N-acyl indole-derived enol carbonates
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title_fullStr | Palladium-catalyzed enantioselective decarboxylative allylic alkylation of fully substituted N-acyl indole-derived enol carbonates
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title_full_unstemmed | Palladium-catalyzed enantioselective decarboxylative allylic alkylation of fully substituted N-acyl indole-derived enol carbonates
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title_short | Palladium-catalyzed enantioselective decarboxylative allylic alkylation of fully substituted N-acyl indole-derived enol carbonates
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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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