一种合成螺-1,3,4-噻二唑啉的方法

IF 1.4 4区化学 Q3 CHEMISTRY, ORGANIC

Chemistry of Heterocyclic Compounds Pub Date : 2024-06-28 DOI:10.1007/s10593-024-03316-0

Alexander V. Komkov, Leonid G. Menchikov, Andrey S. Dmitrenok, Natalya G. Kolotyrkina, Igor V. Zavarzin

引用次数: 0

摘要

通过环酮与氨基甲酸硫酰肼反应合成螺-1,3,4-噻二唑啉的方法被开发出来。高产率地获得了一些新的非甾体螺-1,3,4-噻二唑啉类化合物。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

A method for the synthesis of spiro-1,3,4-thiadiazolines

查看原文本刊更多论文

A method for the synthesis of spiro-1,3,4-thiadiazolines

A method for the synthesis of spiro-1,3,4-thiadiazolines by the reaction of cyclic ketones with oxamic acid thiohydrazides was developed. A number of new nonsteroidal spiro-1,3,4-thiadiazolines was obtained in high yields.

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来源期刊

Chemistry of Heterocyclic Compounds 化学-有机化学

CiteScore

2.90

自引率

13.30%

发文量

审稿时长

1 months

期刊介绍： The international journal Chemistry of Heterocyclic Compounds publishes original papers, short communications, reviews, and mini-reviews dealing with problems in the field of heterocyclic chemistry in Russian and English. The Journal also publishes reviews and annotations on new books and brief reports on conferences in the field of heterocyclic chemistry, as well as commemoratives dedicated to prominent heterocyclic chemists.