201230-92-4Relevant academic research and scientific papers
A highly diastereoselective synthesis of trans-3,4-(difluoromethano)glutamic acid
Shibuya,Kurishita,Ago,Taguchi
, p. 271 - 278 (2007/10/02)
Reaction of enantiomerically pure N-(4'-bromo-4',4'-difluorocrotonoyl)oxazolidinone 5 with lithium enolate of N-diphenylmethylideneglycinate 6 in DMF proceeded in highly diastereoselective manner to give trans-disubstituted gem-difluorocyclopropane 7, which was readily converted to the 3,4-(difluoromethano)glutamic acid 4.
