Deoxofluorination of Aliphatic Carboxylic Acids: A Route to Trifluoromethyl-Substituted Derivatives

被引:21
|
作者
Bugera, Maksym [1 ,2 ]
Trofymchuk, Serhii [1 ,3 ]
Tarasenko, Karen [1 ,2 ]
Zaporozhets, Olga [4 ]
Pustovit, Yurii [1 ,3 ]
Mykhailiuk, Pavel K. [1 ,4 ]
机构
[1] Enamine Ltd, Chervonotkatska 78, UA-02094 Kiev, Ukraine
[2] Natl Acad Sci Ukraine, VP Kukhar Inst Bioorgan Chem & Petrochem, Murmanska 1, UA-02094 Kiev, Ukraine
[3] NAS Ukraine, Inst Organ Chem, Murmanskaya 5, UA-02094 Kiev, Ukraine
[4] Taras Shevchenko Natl Univ Kyiv, Dept Chem, Volodymyrska 64, UA-01601 Kiev, Ukraine
来源
JOURNAL OF ORGANIC CHEMISTRY | 2019年 / 84卷 / 24期
关键词
SULFUR-TETRAFLUORIDE; BUILDING-BLOCKS; SOLID-STATE; FLUORINATION; CHEMISTRY; ARYL; SF4;
D O I
10.1021/acs.joc.9b02596
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A practical method for the synthesis of functionalized aliphatic trifluoromethyl-substituted derivatives from aliphatic acids is developed. The transformation proceeds with sulfur tetrafluoride in the presence of water as a key additive. Compared to previous methods, the reaction gives products with full retention of stereo- and absolute configuration of chiral centers.
引用
收藏
页码:16105 / 16115
页数:11
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