1,6-Addition of 1,2,3-NH triazoles to para-quinone methides: Facile access to highly selective N sup(1) and N sup(2) substituted triazoles

Rai, V.; Kavyashree P.; Harmalkar, S.S.; Dhuri, S.N.; Maddani, M.R.

dc.contributor.author	Rai, V.
dc.contributor.author	Kavyashree P.
dc.contributor.author	Harmalkar, S.S.
dc.contributor.author	Dhuri, S.N.
dc.contributor.author	Maddani, M.R.
dc.date.accessioned	2021-12-17T10:28:23Z
dc.date.available	2021-12-17T10:28:23Z
dc.date.issued	2021
dc.identifier.citation	Organic & Biomolecular Chemistry. 20(2); 2021; 345-351.	en_US
dc.identifier.uri	https://doi.org/10.1039/D1OB01717A
dc.identifier.uri	http://irgu.unigoa.ac.in/drs/handle/unigoa/6629
dc.description.abstract	The regioselective syntheses of N sup(1) and N sup(2) 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 N sup(1)- and N sup(2)-substituted compounds and p-QM related research, the present strategy will greatly benefit researchers in various fields.	en_US
dc.publisher	Royal Society of Chemistry	en_US
dc.subject	Chemistry	en_US
dc.title	1,6-Addition of 1,2,3-NH triazoles to para-quinone methides: Facile access to highly selective N sup(1) and N sup(2) substituted triazoles	en_US
dc.type	Journal article	en_US
dc.identifier.impf	y