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硫(IV)的成键和断键反应:亚砜、锍盐、叶立德和亚磺酸盐。

Bond-Forming and -Breaking Reactions at Sulfur(IV): Sulfoxides, Sulfonium Salts, Sulfur Ylides, and Sulfinate Salts.

机构信息

Institute of Organic Chemistry , University of Vienna , Währinger Strasse 38 , 1090 Vienna , Austria.

出版信息

Chem Rev. 2019 Jul 24;119(14):8701-8780. doi: 10.1021/acs.chemrev.9b00111. Epub 2019 Jun 25.

Abstract

Organosulfur compounds have long played a vital role in organic chemistry and in the development of novel chemical structures and architectures. Prominent among these organosulfur compounds are those involving a sulfur(IV) center, which have been the subject of countless investigations over more than a hundred years. In addition to a long list of textbook sulfur-based reactions, there has been a sustained interest in the chemistry of organosulfur(IV) compounds in recent years. Of particular interest within organosulfur chemistry is the ease with which the synthetic chemist can effect a wide range of transformations through either bond formation or bond cleavage at sulfur. This review aims to cover the developments of the past decade in the chemistry of organic sulfur(IV) molecules and provide insight into both the wide range of reactions which critically rely on this versatile element and the diverse scaffolds that can thereby be synthesized.

摘要

有机硫化合物在有机化学和新型化学结构与架构的发展中一直起着至关重要的作用。在这些有机硫化合物中,最为突出的是那些涉及四价硫中心的化合物,它们在过去一百多年里已经成为无数研究的主题。除了一系列教科书中的基于硫的反应之外,近年来人们对有机硫(IV)化合物的化学也一直保持着浓厚的兴趣。在有机硫化学中特别引人关注的是,合成化学家可以通过在硫原子上形成或断裂键,轻松地实现广泛的转化。本篇综述旨在涵盖过去十年中有机硫(IV)分子化学的发展,并深入了解广泛依赖这种多功能元素的反应以及由此可以合成的各种支架。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c20/6661881/a6e435ef3584/cr-2019-00111k_0001.jpg

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