143546-63-8Relevant academic research and scientific papers
Cyclopropane amino acids that mimic two χ1-conformations of phenylalanine
Moye-Sherman, Destardi,Jin, Song,Li, Shiming,Welch, Michael B.,Reibenspies, Joe,Burgess, Kevin
, p. 2730 - 2739 (1999)
A highly constrained analogue of phenylalanine was prepared in optically pure form. This disubstituted cyclopropane amino acid, DiFi, realises two χ1 values of the phenylalanine side chain. Unlike monosubstituted analogues, amino acids of this
(S)-ABOC: A rigid bicyclic β-amino acid as turn inducer
Andre, Christophe,Legrand, Baptiste,Deng, Cheng,Didierjean, Claude,Pickaert, Guillaume,Martinez, Jean,Averlant-Petit, Marie Christine,Amblard, Muriel,Calmes, Monique
supporting information; body text, p. 960 - 963 (2012/03/27)
In order to investigate the ability of the (S)-aminobicyclo[2.2.2]octane-2- carboxylic acid 1 (H-(S)-ABOC-OH) to induce reverse turns into peptides, two model tripeptides, in which this bicyclic unit was incorporated into the second position, were synthes
