Issue 44, 2021

BF3·Et2O catalyzed transannulation of pyridotriazoles with isothiocyanates: synthesis of thiazolo[3,4-a]pyridin-3-imines

Abstract

The synthesis of thiazolo[3,4-a]pyridin-3-imines through the denitrogenative transannulation of pyridotriazoles with isothiocyanates using BF3·Et2O as a catalyst is described. A combination of solvents (dichlorobenzene-dichloroethane) plays a crucial role in obtaining the desired products under transition metal-free conditions.

Graphical abstract: BF3·Et2O catalyzed transannulation of pyridotriazoles with isothiocyanates: synthesis of thiazolo[3,4-a]pyridin-3-imines

Supplementary files

Article information

Article type
Communication
Submitted
23 Aug 2021
Accepted
15 Oct 2021
First published
18 Oct 2021

New J. Chem., 2021,45, 20547-20550

BF3·Et2O catalyzed transannulation of pyridotriazoles with isothiocyanates: synthesis of thiazolo[3,4-a]pyridin-3-imines

R. Kumar, V. Ginoya, R. Semwal and S. Adimurthy, New J. Chem., 2021, 45, 20547 DOI: 10.1039/D1NJ04033B

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