98737-45-2Relevant academic research and scientific papers
Asymmetric dihydroxylation route to a dipeptide isostere of a protease inhibitor: Enantioselective synthesis of the core unit of ritonavir
Ghosh, Arun K.,Shin, Dongwoo,Mathivanan, Packiarajan
, p. 1025 - 1026 (2007/10/03)
An enantioselective synthesis of the dipeptide isostere of ritonavir has been accomplished utilizing Sharpless asymmetric hydroxylation as the key step.
Peptide inhibitors of aspartic proteinases with hydroxyethylene isostere replacement of peptide bond. II. Preparation of pseudotetrapeptides derived from diastereoisomeric 5-amino-2-benzyl-4-hydroxy-6-phenylhexanoic acids
Litera, Jaroslav,Weber, Jan,Krizova, Ivana,Pichova, Iva,Konvalinka, Jan,Fusek, Martin,Soucek, Milan
, p. 541 - 548 (2007/10/03)
Twelve pseudotetrapeptides, Boc-NHCH(CH2Ph)CH(OH)CH2CH(CH2Ph) CO-Xaa-Phe-NH2 9-11, were prepared by [(benzotriazol-1-yl)oxy]tris(dimethylamino)phosphonium hexafluorophosphatemediated couplings of diastereoisomer
