Tandem approach for the synthesis of 3-sulfenylimidazo1{,}5-apyridines from dithioesters

Ramesha, A. B. and Pavan Kumar, C. S. and Sandhya, N. C. and Kumara, M. N. and Mantelingu, K. and Rangappa, K. S. (2016) Tandem approach for the synthesis of 3-sulfenylimidazo1{,}5-apyridines from dithioesters. RSC Advance, 6. pp. 48375-48378.

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Abstract

Iodine-mediated synthesis of 3-sulfenylimidazo1{,}5-apyridines via C–H functionalization has been achieved using dithioesters{,} 2-methylaminopyridines and sulfonyl hydrazides. A library of 3-sulfanylimidazopyridines and imidazopyridines with broad functionalities are synthesized under metal-free reaction conditions.

Item Type:	Article
Subjects:	C Chemical Science > Chemistry
Divisions:	Department of > Chemistry
Depositing User:	Manjula P Library Assistant
Date Deposited:	01 Jul 2019 06:03
Last Modified:	19 Dec 2020 06:39
URI:	http://eprints.uni-mysore.ac.in/id/eprint/4184

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