Efficient microwave access to polysubstituted amidines from imidoylbenzotriazoles

128Citations
Citations of this article
60Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Microwave reactions of primary and secondary amines with imidoylbenzotriazoles 6a-w gave diversely substituted amidines 7a-Aa in 76-94% yields. Convenient preparations of a variety of amides 5a-Ab (87-96%) and imidoylbenzotriazoles 6a-w (56-95%) have also been developed using microwave irradiation under mild conditions and short reaction times. These results demonstrate further the advantages of microwave synthesis and introduce a new application of imidoylbenzotriazoles in the preparation of polysubstituted amidines. © 2006 American Chemical Society.

Cite

CITATION STYLE

APA

Katritzky, A. R., Cai, C., & Singh, S. K. (2006). Efficient microwave access to polysubstituted amidines from imidoylbenzotriazoles. Journal of Organic Chemistry, 71(9), 3375–3380. https://doi.org/10.1021/jo052443x

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