72015-61-3Relevant articles and documents
PREPARATION OF ALL THE FOUR DIASTEREOMERS OF β-PHENYLCYSTEINE METHYL ESTER THROUGH CHROMATOGRAPHIC OPTICAL RESOLUTION OF THE 2,2-DIMETHYLTHIAZOLIDINE DERIVATIVES
Nagai, Ukon,Pavone, Vincenzo
, p. 589 - 592 (2007/10/02)
cis- And trans-2,2-dimethyl-4-carbomethoxy-5-phenylthiazolidines prepared from the corresponding erythro- and threo-β-phenylcysteines were resolved into the enantiomers by use of a chiral HPLC column, from which all of the four chiral β-phenylcysteine met
N--ΔE-phenylalanine Ethyl Ester
Nitz, Theodore J.,Holt, Elizabeth M.,Rubin, Byron,Stammer, Charles H.
, p. 2667 - 2671 (2007/10/02)
The synthesis of the title compound (1a) has been accomplished by rearrangement of a vinylic isocyanate, and its configuration was confirmed by X-ray crystallography.The configurational stability of 1a to both acids and bases was investigated, and the NMR
Dehydrooligopeptides. I. The facile coupling of α-amino acids with α-dehydroamino acids to dehydrodipeptides
Yonezawa,Shin,Ono,Yoshimura
, p. 2905 - 2909 (2007/10/02)
-