Desulfitative Pd-catalysed coupling reaction using benzenesulfonyl chlorides and enones as the coupling partners-Reference-Cited by-同舟云学术

Desulfitative Pd-catalysed coupling reaction using benzenesulfonyl chlorides and enones as the coupling partners

Published:2015 Issue:5 Volume:5 Page:2904-2912
ISSN:2044-4753
Container-title:Catalysis Science & Technology
language:en
Short-container-title:Catal. Sci. Technol.

Author:

Yuan Kedong¹²³⁴⁵,Sang Rui¹²³⁴⁵,Soulé Jean-François¹²³⁴⁵,Doucet Henri¹²³⁴⁵

Affiliation:

1. Institut Sciences Chimiques de Rennes

2. UMR 6226 CNRS-Université de Rennes “Organométalliques: Matériaux et Catalyse”

3. Campus de Beaulieu

4. 35042 Rennes

5. France

Abstract

The reaction of benzenesulfonyl chlorides with some enones in the presence of a palladium catalyst affords the conjugate addition products instead of the expected Heck type products.

Publisher

Royal Society of Chemistry (RSC)

Subject

Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2015/CY/C5CY00089K

Reference65 articles.

1. M. Oestreich , The Mizoroki–Heck Reaction, Wiley, New York, 2009

2. Intermolecular Dehydrogenative Heck Reactions

3. Pd-Catalyzed Desulfitative Heck Coupling with Dioxygen as the Terminal Oxidant

4. Palladium-Catalyzed Desulfitative Heck-Type Reaction of Aryl Sulfinic Acids with Alkenes

5. Oxidative Mizoroki-Heck-Type Reaction of Arylsulfonyl Hydrazides for a Highly Regio- and Stereoselective Synthesis of Polysubstituted Alkenes

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