75179-53-2Relevant academic research and scientific papers
Chiral sulfonated phosphines. VIII. Hydrogenation of dehydropeptides in a two-phase system
Laghmari, M.,Sinou, D.,Masdeu, A.,Claver, C.
, p. 213 - 216 (1992)
Dehydropeptides have been reduced in a two-phase system using 2> associated with chiral water-soluble ligands derived from cyclobutanediop and BDPP.Diastereoselectivities of up to 87percent were obtained with tetrasulfonated BDPP.
ASYMMETRIC SYNTHESIS OF DIPEPTIDES BY MEANS OF HOMOGENEOUS HYDROGENATION CATALYZED BY CHIRAL RHODIUM COMPLEXES
Ojima, Iwao,Suzuki, Tadashi
, p. 1239 - 1242 (2007/10/02)
Asymmetric hydrogenation of dehydrodipeptides, α-acylaminocinnamoyl-(S)-amino esters catalyzed by rhodium complexes with chiral diphosphines gave either (R)-N-acylphenylalanyl-(S)-aminoesters or (S)-N-acylphenylalanyl-(S)-amino esters with high diastereom
