Synthesis of Thietanes from Saturated Three-membered Heterocycles

被引:14
|
作者
Xu, Jiaxi [1 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Coll Chem, Dept Organ Chem, 15 Northern 3rd Ring Rd East, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
aziridine; epoxide; oxirane; thiirane; thietane; RING-OPENING REACTIONS; DIMETHYLOXOSULFONIUM METHYLIDE; ACYL ISOTHIOCYANATES; SUBSTITUTED TAURINES; MODIFIED TAXOIDS; FACILE SYNTHESIS; ANAL GLAND; DERIVATIVES; ALPHA; SEMISYNTHESIS;
D O I
10.1002/ajoc.202000219
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Thietanes are important structural motifs of some biological compounds and useful intermediates in organic synthesis. Various synthetic methods of thietanes have been developed recently with readily available saturated three-membered heterocycles as starting materials or key intermediates. Both saturated three membered heterocycle-2-methyl halides and sulfonates and thiiranes are widely utilized materials. Both nucleophilic and electrophilic ring expansions of thiiranes are efficient methods for synthesis of thietanes. In this Focus Review, we have described various strategies for the synthesis of strained four-membered thiaheterocyclic thietanes from readily available strained and saturated three-membered heterocycles.
引用
收藏
页码:1008 / 1017
页数:10
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