Tandem approach for the synthesis of 3-sulfenylimidazo[1,5-a]pyridines from dithioesters-Reference-Cited by-同舟云学术

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

Published:2016 Issue:54 Volume:6 Page:48375-48378
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Ramesha Ajjahalli. B.¹²³⁴⁵,Pavan Kumar Chottanahalli. S.¹²³⁴⁵,Sandhya Nagarakere. C.⁶⁷⁸,Kumara Manikyanahalli. N.⁹¹⁰³¹¹⁸,Mantelingu Kempegowda¹²³⁴⁵,Rangappa Kanchugarakoppal. S.¹²³⁴⁵

Affiliation:

1. Synthetic Laboratory

2. DOS in Chemistry

3. University of Mysore

4. Manasagangotri

5. Mysuru-570006

6. Sharada Vilas College

7. Mysuru

8. India

9. Department of Chemistry

10. Yuvaraja's College

11. Mysuru 570005

Abstract

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

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/RA/C6RA03771B

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5. Investigations on the 4-Quinolone-3-carboxylic Acid Motif. 1. Synthesis and Structure−Activity Relationship of a Class of Human Immunodeficiency Virus type 1 Integrase Inhibitors

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