Kamlesh S. Vadagaonkar, Kaliyappan Murugan, Atul C. Chaskar and Prakash M. Bhate
RSC Adv., 2014,4, 34056-34064
DOI:
10.1039/C4RA04961F,
Communication
A mild, efficient and operationally simple one-pot synthesis of substituted [1,2,4]triazolo[4,3-a]pyridines at room temperature from easily available 2-hydrazinopyridine and substituted aromatic aldehydes has been developed. This functional group tolerant and atom-economic method provides facile access to synthetically and biologically important triazolopyridine derivatives.