Fe-Catalyzed Regiodivergent [1, 2]-Shift of α-Aryl Aldehydes

A Gutiérrez-Bonet, A Flores-Gaspar…

Index: Gutierrez-Bonet, Alvaro; Flores-Gaspar, Areli; Martin, Ruben Journal of the American Chemical Society, 2013 , vol. 135, # 34 p. 12576 - 12579

Full Text: HTML

Citation Number: 14

Abstract

An Fe-catalyzed conversion of aldehydes to ketones via [1, 2]-shift has been developed. This skeletal rearrangement shows a wide substrate scope and chemoselectivity profile while exhibiting an excellent [1, 2]-aryl or [1, 2]-alkyl shift selectivity that is easily switched by electronic effects.

Related Articles:

Ruthenium complex catalyzed intermolecular hydroacylation and transhydroformylation of olefins with aldehydes

[Kondo, Teruyuki; Akazome, Motohiro; Tsuji, Yasushi; Watanabe, Yoshihisa Journal of Organic Chemistry, 1990 , vol. 55, # 4 p. 1286 - 1291]

Friedel–Crafts acylation reaction using carboxylic acids as acylating agents

[Kawamura, Masato; Cui, Dong-Mei; Shimada, Shigeru Tetrahedron, 2006 , vol. 62, # 39 p. 9201 - 9209]

Asymmetric reactions. VII. Asymmetric reduction of cyclohexylaryl ketones by optically active alkoxy lithium aluminium hydrides

[Cervinka,O.; Belovsky,O. Collection of Czechoslovak Chemical Communications, 1965 , vol. 30, p. 2487 - 2491]

More Articles...