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An Efficient Synthesis of Disubstituted Pyrazoles From 2-Propyn-1-ol Through Propargyl Hydrazides
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Published in April 2016 Issue 2 (Vol. 6, Issue 2, 2016)

Abstract
An efficient synthesis process access to disubstituted pyrazoles have been demonstrated from 2-propyn-1-alcohols using an effective catalyst Polymer bound pTSA. This conversion proceeds via an acid catalyzed propargylation of N,N-diprotected hydrazines followed by base-mediated cyclization to furnish 3,5-Disubstituted-1H-pyrazoles in optimum yields.
Authors (5)
N. Srinivasan
View all publications →B.Venkateswara Rao
View all publications →J. D. Lilakar
View all publications →Y.L.N. Murthy
View all publications →P. Mahesh
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April 2016 Issue 2 (Vol. 6, Issue 2, 2016)Article Impact
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How to Cite
Srinivasan, N., Rao, B., Lilakar, J. D., Murthy, Y., & Mahesh, P. (2016). An Efficient Synthesis of Disubstituted Pyrazoles From 2-Propyn-1-ol Through Propargyl Hydrazides. American Journal of PharmTech Research, 6(2), 1-7. https://ajptr.com/articles/AJPTR62022
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