Convenient one-pot access to 2H-3-nitrothiochromenes from 2-bromobenzaldehydes, sodium sulfide and β-nitrostyrenes
Author:
Affiliation:
1. Medicinal Chemistry Laboratory
2. Faculty of Chemistry
3. VNU University of Science
4. Ha Noi
5. Vietnam
6. Institut de Chimie des Substances Naturelles
7. CNRS UPR 2301
8. Université Paris-Sud
9. 91198 Gif-sur-Yvette
10. France
Abstract
2H-Thiochromene derivatives have been synthesized using readily available and inexpensive substrates with high functional group tolerance.
Funder
Japan Student Services Organization
Hiroshima University
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2019/OB/C9OB01060B
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3. The antimicrobial natural product chuangxinmycin and Some synthetic analogues are potent and selective inhibitors of bacterial tryptophanyl tRNA synthetase
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