期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 86, 期 17, 页码 11698-11707出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.1c01200
关键词
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A new method for the annulation of a thiopyrane ring to an indole core under mild conditions has been developed. The reaction mechanism involves a stepwise addition through ion-pair formation, with the essential role of the Li atom at all stages of the process being revealed by AIM calculations.
A new approach for the annulation of a thiopyrane ring to an indole core under mild conditions was developed. Treating 2-methyl-3-acylindoles with lithium diisopropyl amide leads to the elimination of a proton from the 2-methyl group. The lithium indole-2,3-dienolates obtained were found to react with CS2 to give the corresponding thiopyrano[4,3-b]indole-3(5H)-thiones. The mechanism represents a stepwise addition through ion-pair formation, according to PCM/B3LYP/6-311++G**, PBE1PBE/6-311++G**, and MP2//HF/6-311++G** quantum chemical calculations. AIM calculations revealed the essential role of the Li atom at all stages of the process.
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