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ppm Pd-catalyzed, Cu-free Sonogashira couplings in water using commercially available catalyst precursors

A new catalyst that derives from commercially available precursors for copper-free, Pd-catalyzed Sonogashira reactions at the sustainable ppm level of precious metal palladium under mild aqueous micellar conditions has been developed. Both the palladium pre-catalyst and ligand are commercially avail...

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Detalles Bibliográficos
Autores principales: Jin, Bo, Gallou, Fabrice, Reilly, John, Lipshutz, Bruce H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6438147/
https://www.ncbi.nlm.nih.gov/pubmed/30996938
http://dx.doi.org/10.1039/c8sc05618h
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author Jin, Bo
Gallou, Fabrice
Reilly, John
Lipshutz, Bruce H.
author_facet Jin, Bo
Gallou, Fabrice
Reilly, John
Lipshutz, Bruce H.
author_sort Jin, Bo
collection PubMed
description A new catalyst that derives from commercially available precursors for copper-free, Pd-catalyzed Sonogashira reactions at the sustainable ppm level of precious metal palladium under mild aqueous micellar conditions has been developed. Both the palladium pre-catalyst and ligand are commercially available, bench stable, and highly cost-effective. The catalyst is applicable to both aryl- and heteroaryl-bromides as educts. A wide range of functional groups are tolerated and the aqueous reaction medium can be recycled. An application to a key intermediate associated with an active pharmaceutical ingredient (ponatinib) is discussed.
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spelling pubmed-64381472019-04-17 ppm Pd-catalyzed, Cu-free Sonogashira couplings in water using commercially available catalyst precursors Jin, Bo Gallou, Fabrice Reilly, John Lipshutz, Bruce H. Chem Sci Chemistry A new catalyst that derives from commercially available precursors for copper-free, Pd-catalyzed Sonogashira reactions at the sustainable ppm level of precious metal palladium under mild aqueous micellar conditions has been developed. Both the palladium pre-catalyst and ligand are commercially available, bench stable, and highly cost-effective. The catalyst is applicable to both aryl- and heteroaryl-bromides as educts. A wide range of functional groups are tolerated and the aqueous reaction medium can be recycled. An application to a key intermediate associated with an active pharmaceutical ingredient (ponatinib) is discussed. Royal Society of Chemistry 2019-01-31 /pmc/articles/PMC6438147/ /pubmed/30996938 http://dx.doi.org/10.1039/c8sc05618h 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
Jin, Bo
Gallou, Fabrice
Reilly, John
Lipshutz, Bruce H.
ppm Pd-catalyzed, Cu-free Sonogashira couplings in water using commercially available catalyst precursors
title ppm Pd-catalyzed, Cu-free Sonogashira couplings in water using commercially available catalyst precursors
title_full ppm Pd-catalyzed, Cu-free Sonogashira couplings in water using commercially available catalyst precursors
title_fullStr ppm Pd-catalyzed, Cu-free Sonogashira couplings in water using commercially available catalyst precursors
title_full_unstemmed ppm Pd-catalyzed, Cu-free Sonogashira couplings in water using commercially available catalyst precursors
title_short ppm Pd-catalyzed, Cu-free Sonogashira couplings in water using commercially available catalyst precursors
title_sort ppm pd-catalyzed, cu-free sonogashira couplings in water using commercially available catalyst precursors
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6438147/
https://www.ncbi.nlm.nih.gov/pubmed/30996938
http://dx.doi.org/10.1039/c8sc05618h
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