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铑催化的涉及二硫键和硫的 S-S 键断裂的有机硫化合物的合成。

Rhodium-Catalyzed Synthesis of Organosulfur Compounds Involving S-S Bond Cleavage of Disulfides and Sulfur.

机构信息

Department of Organic Chemistry, Graduate School of Pharmaceutical Sciences, Tohoku University, Aoba, Sendai 980-8578, Japan.

出版信息

Molecules. 2020 Aug 7;25(16):3595. doi: 10.3390/molecules25163595.

Abstract

Organosulfur compounds are widely used for the manufacture of drugs and materials, and their synthesis in general conventionally employs nucleophilic substitution reactions of thiolate anions formed from thiols and bases. To synthesize advanced functional organosulfur compounds, development of novel synthetic methods is an important task. We have been studying the synthesis of organosulfur compounds by transition-metal catalysis using disulfides and sulfur, which are easier to handle and less odiferous than thiols. In this article, we describe our development that rhodium complexes efficiently catalyze the cleavage of S-S bonds and transfer organothio groups to organic compounds, which provide diverse organosulfur compounds. The synthesis does not require use of bases or organometallic reagents; furthermore, it is reversible, involving chemical equilibria and interconversion reactions.

摘要

有机硫化合物被广泛用于药物和材料的制造,其合成通常采用巯基和碱形成的硫负离子的亲核取代反应。为了合成先进的功能性有机硫化合物,开发新的合成方法是一项重要任务。我们一直在研究使用二硫化物和硫作为过渡金属催化剂合成有机硫化合物,它们比巯基更容易处理,气味也更小。在本文中,我们描述了我们的研究进展,即铑配合物有效地催化 S-S 键的断裂,并将有机硫基团转移到有机化合物上,从而提供了多种有机硫化合物。该合成不需要使用碱或有机金属试剂;此外,它是可逆的,涉及化学平衡和相互转化反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8c5/7464046/96df76a9adf7/molecules-25-03595-g001.jpg

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