Tandem approach for the synthesis of 3-sulfenylimidazo[1,5-a]pyridines from dithioesters

201629 citationsJournal Article

Authors

Ajjahalli B. Ramesha · Synthetic Biologics (United States)

Chottanahalli S. Pavan Kumar · Intelligent Synthetic Biology Center

Nagarakere C. Sandhya · Vilnius College of Design

M. N. Kumara · University of Mysore

Kempegowda Mantelingu · State Key Laboratory of Synthetic Chemistry

Kanchugarakoppal S. Rangappa · Intelligent Synthetic Biology Center

Abstract

Iodine-mediated synthesis of 3-sulfenylimidazo[1,5-<italic>a</italic>]pyridines<italic>via</italic>C–H functionalization has been achieved using dithioesters, 2-methylaminopyridines and sulfonyl hydrazides.

Topics & Keywords

Sulfur-Based Synthesis Techniques Catalytic C–H Functionalization Methods Synthesis and Catalytic Reactions

Publication Details

Published in: RSC Advances

Volume 6, Issue 54, pp. 48375-48378

DOI: 10.1039/c6ra03771b

Field-Weighted Citation Impact: 1.89

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Tandem approach for the synthesis of 3-sulfenylimidazo[1,5-a]pyridines from dithioesters

Authors

Abstract

Topics & Keywords

Publication Details