1403953-59-2Relevant academic research and scientific papers
Stereoselective synthesis of both enantiomers of trans-2- (diphenylmethylideneamino)cyclopropanecarboxylic acid using a chiral pool approach and their incorporation in dipeptides
Meiresonne, Tamara,Mangelinckx, Sven,De Kimpe, Norbert
, p. 9566 - 9571,6 (2020/08/20)
The stereoselective synthesis of (1R,2R)- and (1S,2S)-trans-2- (diphenylmethylideneamino)cyclopropanecarboxylic acid has been accomplished in six steps starting from (2S)- and (2R)-β-benzyl N-(tert-butoxycarbonyl) aspartate, respectively. The key-step in
