Asymmetric Access to Chiral Sulfinyl Compounds as Bioisosteres of Carbonyl Compounds

被引:0
|
作者
Wang, Chenxin [1 ]
Wu, Xinyu [2 ]
Huang, Jiapian [2 ]
Liu, Gang [1 ]
Wu, Jie [2 ,3 ,4 ]
机构
[1] Jiangxi Sci & Technol Normal Univ, Jiangxi Key Lab Organ Chem, Nanchang 330013, Peoples R China
[2] Taizhou Univ, Inst Adv Studies, 1139 Shifu Ave, Taizhou 318000, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organomet Chem, 345 Lingling Rd, Shanghai 200032, Peoples R China
[4] Henan Normal Univ, Sch Chem & Chem Engn, Xinxiang 453007, Peoples R China
来源
SYNTHESIS-STUTTGART | 2024年 / 56卷 / 17期
基金
中国国家自然科学基金;
关键词
sulfinyl; bioisostere; asymmetric synthesis; sulfoxide; sulfinate ester; sulfinamide; PARALLEL KINETIC RESOLUTION; C-H ACTIVATION; CATALYZED ENANTIOSELECTIVE ARYLATION; TERT-BUTYL SULFOXIDES; SULFENATE ANIONS; GAMMA-SULTINES; BOND FORMATION; REGIODIVERGENT; SULFINAMIDES; OXIDATION;
D O I
10.1055/a-2335-8452
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
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.
引用
收藏
页码:2648 / 2654
页数:7
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