Continuous flow strategies for using fluorinated greenhouse gases in fluoroalkylations

被引:53
作者
Fu, Wai Chung [1 ,2 ]
MacQueen, Preston M. [1 ,3 ]
Jamison, Timothy F. [1 ]
机构
[1] MIT, Dept Chem, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[2] Hong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Hung Hom, Kowloon, Hong Kong, Peoples R China
[3] MilliporeSigma, Dept Res & Dev, 6000 N Teutonia Ave, Milwaukee, WI 53209 USA
基金
加拿大自然科学与工程研究理事会;
关键词
PHOTOCATALYTIC TRIFLUOROMETHYLATION; DIRECT CUPRATION; PHOTOREDOX CATALYSIS; FLUOROFORM; DIFLUOROMETHYLATION; DIFLUOROCARBENE; PERFLUOROALKYLATION; PHASE; BATCH; MILD;
D O I
10.1039/d0cs00670j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Large quantities of fluorinated gases are generated as intermediates or byproducts from fluorinated polymer production annually, and they are effective ozone depleting substances or greenhouse gases. On the other hand, the incorporation of fluoroalkyl groups into drug molecules or bioactive compounds has been shown to enhance biological properties such as the bioavailability, binding selectivity, and metabolic stability. Extraction of fluoroalkyl sources, including trifluoromethyl and difluoromethyl groups, from the fluorinated gases is highly desirable, yet challenging under regular batch reaction conditions. Flow chemistry is an emerging and promising technique to address long-standing challenges in gas-liquid batch reactions such as insufficient interfacial contact and scalability issues. In this review, we highlight recent advances in continuous flow strategies toward enabling the use of fluorinated greenhouse gases in organic synthesis.
引用
收藏
页码:7378 / 7394
页数:17
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