Three-component synthesis of α-amino-α-aryl carbonitriles from arynes, aroyl cyanides, and N,N-dimethylformamide

23Citations
Citations of this article
5Readers
Mendeley users who have this article in their library.
Get full text

Abstract

A general and efficient synthesis of α-amino-α-aryl carbonitriles through the three-component reaction of arynes, aroyl cyanides, and DMF in a single step is described. DMF was not only used as the solvent, but it also participated in the reaction as a component. Used as the cyanide sources, the aroyl cyanides solved the toxicity and solubility problems associated with the use of HCN or metal cyanides in the Strecker synthesis. This procedure furnished α-amino-α-aryl carbonitriles in moderate to good yields with broad substrate scope. Moreover, this reaction could be performed under mild conditions with high atom economy. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Cite

CITATION STYLE

APA

Zhou, C., Wang, J., Jin, J., Lu, P., & Wang, Y. (2014). Three-component synthesis of α-amino-α-aryl carbonitriles from arynes, aroyl cyanides, and N,N-dimethylformamide. European Journal of Organic Chemistry, 2014(9), 1832–1835. https://doi.org/10.1002/ejoc.201400040

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free