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Minimising conformational bias in fluoroprolines through vicinal difluorination†‡
Emile Ottoy,Mark E. Light,Bruno Kieffer,Ilya Kuprov,Jose C. Martins,Davy Sinnaeve,Bruno Linclau
Chemical Communications Pub Date : 04/16/2018 00:00:00 , DOI:10.1039/C8CC01493K
Abstract

Monofluorination at the proline 4-position results in conformational effects, which is exploited for a range of applications. However, this conformational distortion is a hindrance when the natural proline conformation is important. Here we introduce (3S,4R)-3,4-difluoroproline, in which the individual fluorine atoms instil opposite conformational effects, as a suitable probe for fluorine NMR studies.

Graphical abstract: Minimising conformational bias in fluoroprolines through vicinal difluorination
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