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Synthesis
DOI: 10.1055/a-2335-8452
DOI: 10.1055/a-2335-8452
paper
Bioisosteres
Asymmetric Access to Chiral Sulfinyl Compounds as Bioisosteres of Carbonyl Compounds
Financial support from the National Natural Science Foundation of China (22171206), the Natural Science Foundation of Zhejiang Province (LZ23B020001), the Zhejiang Provincial Ten Thousand Talent Program (2023R5244) and the Open Research Fund of School of Chemistry and Chemical Engineering, Henan Normal University (2020ZD04) is gratefully acknowledged.
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
Publication History
Received: 03 April 2024
Accepted after revision: 29 May 2024
Accepted Manuscript online:
29 May 2024
Article published online:
18 June 2024
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