Asymmetric Access to Chiral Sulfinyl Compounds as Bioisosteres of Carbonyl Compounds

Synthesis Pub Date : 2024-06-18 DOI:10.1055/a-2335-8452
Chenxin Wang, Xinyu Wu, Jiapian Huang, Gang Liu, Jie Wu
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Abstract

The sulfinyl group, as one of the bioisosteres of carbonyl groups, attracts considerable attention in the field of synthetic chemistry. In particular, the asymmetric construction of chiral sulfinyl compounds and their derivatives remains in the early stages of development. Sulfinyl compounds mainly include sulfoxides, sulfinate esters and sulfinamides, according to the different functional groups connected to the sulfur atom. This Review summarizes the fascinating recent progress made over the past decade on the asymmetric synthesis of enantiopure sulfinyl derivatives.

1 Introduction

2 Asymmetric Synthesis of Chiral Sulfoxides

3 Asymmetric Synthesis of Chiral Sulfinate Esters

4 Asymmetric Synthesis of Chiral Sulfinamides

5 Conclusion and Outlook

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不对称获取手性亚磺酰化合物作为羰基化合物的生物异养生物
亚磺酰基作为羰基的生物异构体之一,在合成化学领域备受关注。特别是手性亚砜基化合物及其衍生物的不对称结构仍处于早期开发阶段。根据与硫原子相连的不同官能团,亚磺酰化合物主要包括亚砜、亚砜酯和亚磺酰胺。本综述总结了过去十年中在不对称合成对映体纯亚磺酰衍生物方面取得的最新进展。1 引言 2 手性硫醚的不对称合成 3 手性硫酸酯的不对称合成 4 手性亚磺酰胺的不对称合成 5 结论与展望
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