A Single Phosphine Ligand Allows Palladium-Catalyzed Intermolecular C-O Bond Formation with Secondary and Primary Alcohols

Forging a bond: An efficient, general palladium catalyst for C-O bond-forming reactions of secondary and primary alcohols with a range of aryl halides has been developed using the ligand 1. Heteroaryl halides, and for the first time, electron-rich aryl halides can be coupled with secondary alcohols....

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Main Authors: Wu, Xiaoxing, Fors, Brett P., Buchwald, Stephen Leffler
Other Authors: Massachusetts Institute of Technology. Department of Chemistry
Format: Article
Language:en_US
Published: Wiley Blackwell 2013
Online Access:http://hdl.handle.net/1721.1/81973
https://orcid.org/0000-0003-3875-4775
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author Wu, Xiaoxing
Fors, Brett P.
Buchwald, Stephen Leffler
author2 Massachusetts Institute of Technology. Department of Chemistry
author_facet Massachusetts Institute of Technology. Department of Chemistry
Wu, Xiaoxing
Fors, Brett P.
Buchwald, Stephen Leffler
author_sort Wu, Xiaoxing
collection MIT
description Forging a bond: An efficient, general palladium catalyst for C-O bond-forming reactions of secondary and primary alcohols with a range of aryl halides has been developed using the ligand 1. Heteroaryl halides, and for the first time, electron-rich aryl halides can be coupled with secondary alcohols. A diverse set of substrate combinations are possible with just a single ligand, thus obviating the need to survey multiple ligands.
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spelling mit-1721.1/819732022-10-01T12:27:43Z A Single Phosphine Ligand Allows Palladium-Catalyzed Intermolecular C-O Bond Formation with Secondary and Primary Alcohols Wu, Xiaoxing Fors, Brett P. Buchwald, Stephen Leffler Massachusetts Institute of Technology. Department of Chemistry Wu, Xiaoxing Fors, Brett P. Buchwald, Stephen Leffler Forging a bond: An efficient, general palladium catalyst for C-O bond-forming reactions of secondary and primary alcohols with a range of aryl halides has been developed using the ligand 1. Heteroaryl halides, and for the first time, electron-rich aryl halides can be coupled with secondary alcohols. A diverse set of substrate combinations are possible with just a single ligand, thus obviating the need to survey multiple ligands. National Institutes of Health (U.S.) (Grant GM-58160) Amgen Inc. Bristol-Myers Squibb Company (Graduate Fellowship) National Institutes of Health (U.S.) (GM 1S10RR13886-01) 2013-11-04T16:59:00Z 2013-11-04T16:59:00Z 2011-09 2011-06 Article http://purl.org/eprint/type/JournalArticle 14337851 1521-3773 http://hdl.handle.net/1721.1/81973 Wu, Xiaoxing, Brett P. Fors, and Stephen L. Buchwald. “A Single Phosphine Ligand Allows Palladium-Catalyzed Intermolecular C-O Bond Formation with Secondary and Primary Alcohols.” Angewandte Chemie International Edition 50, no. 42 (October 10, 2011): 9943-9947. https://orcid.org/0000-0003-3875-4775 en_US http://dx.doi.org/10.1002/anie.201104361 Angewandte Chemie International Edition Creative Commons Attribution-Noncommercial-Share Alike 3.0 http://creativecommons.org/licenses/by-nc-sa/3.0/ application/pdf Wiley Blackwell PMC
spellingShingle Wu, Xiaoxing
Fors, Brett P.
Buchwald, Stephen Leffler
A Single Phosphine Ligand Allows Palladium-Catalyzed Intermolecular C-O Bond Formation with Secondary and Primary Alcohols
title A Single Phosphine Ligand Allows Palladium-Catalyzed Intermolecular C-O Bond Formation with Secondary and Primary Alcohols
title_full A Single Phosphine Ligand Allows Palladium-Catalyzed Intermolecular C-O Bond Formation with Secondary and Primary Alcohols
title_fullStr A Single Phosphine Ligand Allows Palladium-Catalyzed Intermolecular C-O Bond Formation with Secondary and Primary Alcohols
title_full_unstemmed A Single Phosphine Ligand Allows Palladium-Catalyzed Intermolecular C-O Bond Formation with Secondary and Primary Alcohols
title_short A Single Phosphine Ligand Allows Palladium-Catalyzed Intermolecular C-O Bond Formation with Secondary and Primary Alcohols
title_sort single phosphine ligand allows palladium catalyzed intermolecular c o bond formation with secondary and primary alcohols
url http://hdl.handle.net/1721.1/81973
https://orcid.org/0000-0003-3875-4775
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