Selective halocyclization and iodosulfonylation of <i>N</i>-benzothiazol-2-yl alkynamides under mild conditions-Reference-Cited by-同舟云学术

Selective halocyclization and iodosulfonylation of N-benzothiazol-2-yl alkynamides under mild conditions

Published:2022 Issue:33 Volume:20 Page:6550-6553
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Fang Yu¹,Ren Shangfeng¹,He Chen²,Han Huiqi²,Liu Jin-Biao¹^ORCID,Liao Fumin¹,Yang Min²^ORCID

Affiliation:

1. Jiangxi Provincial Key Laboratory of Functional Molecular Materials Chemistry, Jiangxi University of Science and Technology, Ganzhou 341000, China

2. Key Laboratory of Biomaterials and Biofabrication in Tissue Engineering of Jiangxi Province, Key Laboratory of Biomedical Sensors of Ganzhou, School of Pharmacy, School of Basic Medicine, Gannan Medical University, Ganzhou, 341000, China

Abstract

The selective halocyclization and iodosulfonylation of N-benzothiazol-2-yl alkynamides under mild conditions is described, affording pyrimidobenzothiazoles and multisubstituted α,β-enones respectively.

Funder

Science Fund for Distinguished Young Scholars of Jiangxi Province

Education Department of Jiangxi Province

Gannan Medical University

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/OB/D2OB01165D

Reference43 articles.