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Ligand-assisted palladium-catalyzed C–H alkenylation of aliphatic amines for the synthesis of functionalized pyrrolidines

The development of a ligand-assisted Pd-catalyzed C–H alkenylation of aliphatic amines is reported. Our studies indicated that an amino-acid-derived ligand renders the C–H bond activation step reversible and promotes the traditionally difficult alkenylation process. The C(sp(3))–H alkenylation proce...

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Autores principales: He, Chuan, Gaunt, Matthew J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6092717/
https://www.ncbi.nlm.nih.gov/pubmed/30155203
http://dx.doi.org/10.1039/c7sc00468k
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author He, Chuan
Gaunt, Matthew J.
author_facet He, Chuan
Gaunt, Matthew J.
author_sort He, Chuan
collection PubMed
description The development of a ligand-assisted Pd-catalyzed C–H alkenylation of aliphatic amines is reported. Our studies indicated that an amino-acid-derived ligand renders the C–H bond activation step reversible and promotes the traditionally difficult alkenylation process. The C(sp(3))–H alkenylation proceeds through a 5-membered-ring cyclopalladation pathway that allows access to complex aliphatic heterocycles that could be useful to practioners of synthetic and medicinal chemistry.
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spelling pubmed-60927172018-08-28 Ligand-assisted palladium-catalyzed C–H alkenylation of aliphatic amines for the synthesis of functionalized pyrrolidines He, Chuan Gaunt, Matthew J. Chem Sci Chemistry The development of a ligand-assisted Pd-catalyzed C–H alkenylation of aliphatic amines is reported. Our studies indicated that an amino-acid-derived ligand renders the C–H bond activation step reversible and promotes the traditionally difficult alkenylation process. The C(sp(3))–H alkenylation proceeds through a 5-membered-ring cyclopalladation pathway that allows access to complex aliphatic heterocycles that could be useful to practioners of synthetic and medicinal chemistry. Royal Society of Chemistry 2017-05-01 2017-02-23 /pmc/articles/PMC6092717/ /pubmed/30155203 http://dx.doi.org/10.1039/c7sc00468k Text en This journal is © The Royal Society of Chemistry 2017 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0)
spellingShingle Chemistry
He, Chuan
Gaunt, Matthew J.
Ligand-assisted palladium-catalyzed C–H alkenylation of aliphatic amines for the synthesis of functionalized pyrrolidines
title Ligand-assisted palladium-catalyzed C–H alkenylation of aliphatic amines for the synthesis of functionalized pyrrolidines
title_full Ligand-assisted palladium-catalyzed C–H alkenylation of aliphatic amines for the synthesis of functionalized pyrrolidines
title_fullStr Ligand-assisted palladium-catalyzed C–H alkenylation of aliphatic amines for the synthesis of functionalized pyrrolidines
title_full_unstemmed Ligand-assisted palladium-catalyzed C–H alkenylation of aliphatic amines for the synthesis of functionalized pyrrolidines
title_short Ligand-assisted palladium-catalyzed C–H alkenylation of aliphatic amines for the synthesis of functionalized pyrrolidines
title_sort ligand-assisted palladium-catalyzed c–h alkenylation of aliphatic amines for the synthesis of functionalized pyrrolidines
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6092717/
https://www.ncbi.nlm.nih.gov/pubmed/30155203
http://dx.doi.org/10.1039/c7sc00468k
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