硫酰胺与亚氨基碘烷的反应:1,2-噻嗪、噻吩和磺酰基异噻唑啉的研究

IF 3.6 2区 化学 Q1 CHEMISTRY, ORGANIC
Vladimir G. Ilkin*, Ilya D. Gridnev, Mikhail S. Novikov, Pavel S. Silaichev, Tetyana V. Beryozkina, Pavel A. Slepukhin, Wim Dehaen and Vasiliy A. Bakulev*, 
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引用次数: 0

摘要

介绍了过渡金属催化和非催化的丙烯酸硫酰胺与N-磺酰氨基碘烷的反应,在温和条件下选择性合成了一系列全修饰S和含N,S的杂环。硫酰胺结构的微调允许选择性制备收率高的邻熔噻吩、1,2-噻嗪和螺熔异噻唑啉。发现了一锅热诱导的磺基异噻唑啉重排作为噻吩的补充途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Reactions of Thioamides with Iminoiodinanes: An Approach toward 1,2-Thiazines, Thiophenes, and Sulfonylisothiazolines

Reactions of Thioamides with Iminoiodinanes: An Approach toward 1,2-Thiazines, Thiophenes, and Sulfonylisothiazolines

Transition metal-catalyzed and noncatalytic reactions of acrylic thioamides with N-sulfonyliminoiodinanes enabling the selective synthesis under mild conditions of a series of fully decorated S- and N,S-containing heterocycles are described. Fine-tuning of the thioamide structure allows selective preparation in good yields of ortho-fused thiophenes, 1,2-thiazines, and spiro-fused isothiazolines. A one-pot thermally induced rearrangement of sulfonylisothiazolines was discovered as a complementary route to thiophenes.

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来源期刊
Journal of Organic Chemistry
Journal of Organic Chemistry 化学-有机化学
CiteScore
6.20
自引率
11.10%
发文量
1467
审稿时长
2 months
期刊介绍: Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.
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