Issue 6, 2010

Brønsted acid-catalyzed efficient Strecker reaction of ketones, amines and trimethylsilyl cyanide

Abstract

A general method for the one-pot, three-component Strecker reaction of ketones was developed using Brønsted acids as organocatalysts. A series of α-aminonitriles were obtained in good to excellent yields (79–99%). A preliminary extension to a catalytic enantioselective three-component Strecker reaction of ketones (up to 40% ee) is also described.

Graphical abstract: Brønsted acid-catalyzed efficient Strecker reaction of ketones, amines and trimethylsilyl cyanide

Supplementary files

Article information

Article type
Paper
Submitted
19 Nov 2009
Accepted
17 Dec 2009
First published
20 Jan 2010

Org. Biomol. Chem., 2010,8, 1399-1405

Brønsted acid-catalyzed efficient Strecker reaction of ketones, amines and trimethylsilyl cyanide

G. Zhang, D. Zheng, J. Nie, T. Wang and J. Ma, Org. Biomol. Chem., 2010, 8, 1399 DOI: 10.1039/B924272D

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