Issue 2, 2022

1,6-Addition of 1,2,3-NH triazoles to para-quinone methides: Facile access to highly selective N1 and N2 substituted triazoles

Abstract

The regioselective syntheses of N1 and N2 substituted triazoles through a 1,6-addition reaction of 1,2,3-NH triazoles to p-quinone methide were achieved under mild reaction conditions. The present reactions showed superior results in terms of selectivity, mild reaction conditions, short reaction time and broad substrate scope with good functional-group compatibility. Considering the high synthetic value of N1- and N2-substituted compounds and p-QM related research, the present strategy will greatly benefit researchers in various fields.

Graphical abstract: 1,6-Addition of 1,2,3-NH triazoles to para-quinone methides: Facile access to highly selective N1 and N2 substituted triazoles

Supplementary files

Article information

Article type
Communication
Submitted
01 Sep 2021
Accepted
24 Nov 2021
First published
15 Dec 2021

Org. Biomol. Chem., 2022,20, 345-351

1,6-Addition of 1,2,3-NH triazoles to para-quinone methides: Facile access to highly selective N1 and N2 substituted triazoles

V. Rai, K. P., S. S. Harmalkar, S. N. Dhuri and M. R. Maddani, Org. Biomol. Chem., 2022, 20, 345 DOI: 10.1039/D1OB01717A

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