Quaternary Stereogenic Centers through Enantioselective Heck Arylation of Acyclic Olefins with Aryldiazonium Salts: Application in a Concise Synthesis of (R)-Verapamil-Reference-Cited by-同舟云学术

Quaternary Stereogenic Centers through Enantioselective Heck Arylation of Acyclic Olefins with Aryldiazonium Salts: Application in a Concise Synthesis of (R)-Verapamil

Published:2015-09-25 Issue:47 Volume:54 Page:14036-14039
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Oliveira Caio C.,Pfaltz Andreas,Correia Carlos Roque Duarte

Funder

São Paulo Research Foundation

Swiss National Science Foundation

Publisher

Wiley

Subject

General Chemistry,Catalysis

Reference51 articles.

1. The Heck Reaction as a Sharpening Stone of Palladium Catalysis

2. Non-conventional methodologies for transition-metal catalysed carbon–carbon coupling: a critical overview. Part 1: The Heck reaction

3. Diazonium Salts as Substrates in Palladium-Catalyzed Cross-Coupling Reactions

4. Evolution and Synthetic Applications of the Heck–Matsuda Reaction: The Return of Arenediazonium Salts to Prominence

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