Facile synthesis of (polyfluoro)alkanesulfinyl 4-isoxazolines: a stepwise solvent- and catalyst-free approach or a one-pot process in water

被引:10
作者
Liao, Tian-Ming [1 ]
Ma, Wen-Jiang [1 ]
Gao, Yu-Ning [1 ]
Bian, Ming [1 ]
Jiang, Min [2 ]
Liu, Jin-Tao [2 ]
Chen, Hui-Yu [1 ]
Liu, Zhen-Jiang [1 ,2 ]
机构
[1] Shanghai Inst Technol, Sch Chem & Environm Engn, 100 Haiquan Rd, Shanghai 201418, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Organ Chem, Key Lab Organofluorine Chem, 345 Lingling Rd, Shanghai 200032, Peoples R China
基金
中国国家自然科学基金;
关键词
3+2 CYCLOADDITION; 1,3-DIPOLAR CYCLOADDITION; NITRONES; REACTIVITY; TRIFLUOROMETHYLTHIOLATION; HYDROXYLAMINES; DIPOLAROPHILES; CYCLIZATION; PYRROLES; ALLENES;
D O I
10.1039/d3gc00557g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
4-Isoxazolines are important motifs in various biologically interesting molecules and versatile synthons for the preparation of various cyclic and acyclic compounds. Herein, two green and facile protocols were reported for the synthesis of a wide range of polyfluoroalkanesulfinyl or alkylsulfinyl 4-isoxazolines. A variety of aldehyde and ketone derived nitrones reacted with alpha-alkynyl sulfoxides under catalyst- and solvent-free conditions at room temperature to provide a series of polyfluoroalkanesulfinyl or alkylsulfinyl 4-isoxazolines with high efficiency. The synthesis of these sulfinyl 4-isoxazolines was further improved to a one-pot process in aqueous medium starting from aldehydes and hydroxylamine hydrochlorides without the need for isolating the nitrones. The reactions developed in this work are easy to perform and demonstrate significant ecological advantages.
引用
收藏
页码:5233 / 5239
页数:7
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