Journal
GREEN CHEMISTRY
Volume 18, Issue 2, Pages 402-405Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c5gc01821h
Keywords
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Funding
- Natural Science Foundation of China [21562025]
- Natural Science Foundation of Jiangxi Province [20151BAB203008]
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The cascade reactions between enaminones and o-aminothiophenols have been implemented to provide unprecedented vicinal diketones containing benzothiazole structures. The construction of the products has been realized under metal-free conditions via carbonylation on the C=C double bond of the enaminone. The tunable synthesis of 2-aroylbenzothiazoles has been achieved by using identical starting materials under modified reaction conditions.
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