129397-84-8Relevant academic research and scientific papers
Arg-Gly thiomethylene dipeptide surrogates: Synthesis and incorporation into Arg-Gly-Asp pseudotripeptides
Harn, Nancy K.,Cripps, Stephan J.,Rishton, Gilbert M.
, p. 1389 - 1392 (1994)
A synthesis of Arg-Gly thiomethylene dipeptide surrogates and the incorporation of these surrogates into Arg-Gly-Asp type pseudotripeptides are described. These compounds are potentially useful for the preparation of small nonpeptide Arg-Gly-Asp peptidomimetics and may find general utility in the fields of peptide chemistry and protein engineering.
PREPARATION OF N-PROTECTED α-AMINO ALCOHOLS BY ACETOXYBOROHYDRIDE REDUCTION OF N-PROTECTED α-AMINO ACID ESTERS
Soucek, Milan,Urban, Jan,Saman, David
, p. 761 - 765 (2007/10/02)
N-Protected α-amino alcohols were prepared by reduction of N-protected α-amino acid esters by sodium acetoxyborohydride in dioxane at elevated temperature.The reductions proceed with excellent yields and without racemisation.Reduction of the carbamate protecting groups was not observed.
