177723-39-6Relevant articles and documents
STEREOSELECTIVE SYNTHESIS OF N-BOC-O-BENZYL-(4S,5S)-5-AMINO-4-HYDROXY-6-PHENYLHEXANOIC ACID, THE HYDROXYETHYLENE ISOSTERIC MOIETY OF POTENT HIV-1 PROTEASE INHIBITOR
Chakraborty, T. K.,Gangakhedkar, Kiran Kumar
, p. 1897 - 1898 (1991)
N-Boc-O-benzyl-(4S,5S)-5-amino-4-hydroxy-6-phenylhexanoic acid is synthesized in a highly stereoselective way involving, as a key step, regioselective opening of carbohydrate-based aziridine ring.
Total synthesis of enantiomerically pure (-)-Balanol
Barbier, Pierre,Stadlwieser, Josef
, p. 530 - 532 (2007/10/03)
The total synthesis of enantiomerically pure (-)-Balanol (1), using tri-O-acetyl-D-glucal as a chiral template for the central azepane fragment is described.