z-logo
Premium
Silver‐Catalyzed Cross‐Coupling of Isocyanides and Active Methylene Compounds by a Radical Process
Author(s) -
Liu Jianquan,
Liu Zhenhua,
Liao Peiqiu,
Zhang Lin,
Tu Tao,
Bi Xihe
Publication year - 2015
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.201504254
Subject(s) - methylene , isomerization , catalysis , chemistry , surface modification , combinatorial chemistry , ligand (biochemistry) , coupling reaction , photochemistry , organic chemistry , biochemistry , receptor
Abstract Isocyanides are versatile building blocks, and have been extensively exploited in CH functionalization reactions. However, transition‐metal‐catalyzed direct CH functionalization reactions with isocyanides suffer from over‐insertion of isocyanides. Reported herein is a radical coupling/isomerization strategy for the cross‐coupling of isocyanides with active methylene compounds through silver‐catalysis. The method solves the over‐insertion issue and affords a variety of otherwise difficult to synthesize β‐aminoenones and tricarbonylmethanes under base‐ and ligand‐free conditions. This report presents a new fundamental CC bond‐forming reaction of two basic chemicals.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here