Intercepting the Gold-Catalysed Meyer-Schuster Rearrangement by Controlled Protodemetallation: A Regioselective Hydration of Propargylic Alcohols-Reference-Cited by-同舟云学术

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Intercepting the Gold-Catalysed Meyer-Schuster Rearrangement by Controlled Protodemetallation: A Regioselective Hydration of Propargylic Alcohols

Published:2016-04-27 Issue:9 Volume:358 Page:1519-1525
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Pennell Matthew N.¹,Kyle Michael P.²,Gibson Samantha M.¹,Male Louise²,Turner Peter G.³,Grainger Richard S.²,Sheppard Tom D.¹

Affiliation:

1. Department of Chemistry, University College London; Christopher Ingold Laboratories; 20 Gordon Street London WC1H 0AJ U.K.

2. School of Chemistry; University of Birmingham; Edgbaston, Birmingham B15 2TT U.K.

3. GlaxoSmithKline; Medicines Research Centre; Gunnels Wood Road Stevenage, Herts SG1 2NY U.K.

Funder

Engineering and Physical Sciences Research Council (EPSRC)

GlaxoSmithKline

Department of Chemistry at University College London

University of Birmingham

Publisher

Wiley

Subject

General Chemistry

Reference56 articles.

1. Transition-Metal-Catalyzed Functionalization of Propargylic Alcohols and Their Derivatives

2. Recent Advances on the Lewis Acid-Catalyzed Cascade Rearrangements of Propargylic Alcohols and Their Derivatives

3. [(NHC)AuCl]-catalyzed Meyer–Schuster rearrangement: scope and limitations

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