Density functional (BHandH) calculations, using 6-31G** basis set, have been employed to study the reaction mechanism of the enantioselectivity in a chiral 1,3,2-oxazaphospholidine-borane cata- lyzed reduction of acetophenone.

Synthesis and Antibacterial Activity of(S)-5-Acetamidomethyl-3-[(3-chloro-4-substituted aminomethyl)phenyl]-2-oxazolidinones;

Linezolid is a new class of oxazolidinones antibacterial agents that has been first used in clinical,it inhibits bacterial protein synthesis by blocking the formation of initiation complex.

The oxazolidinones are a new class of totally synthetic antibacterials that inhibit protein synthesis via binding to a distinct region of 23S RNA of the 50S ribosomal subunit in prokaryotes.

Analysis of (4S)-4-benzyl-3-(2′(E)-butenyl)-2-oxazolidinone by nuclear magnetic resonance;

Studies on synthesis of NCPS supported oxazolidinone chiral auxiliary;

Preparation of (S)-(+)-4-Phenyl-2-oxazolidinone;

Dimeric Catechin-oxazolidine Tannage and Histological Modality of Fore-and-aft Leather Shrinkage;

Resorcin-oxazolidine Combination Tannage;

THP-oxazolidine-fish Oil Tanning Leather

The asymmetric reduction of ketosulfone with borane catalyzed by oxazaborolidine is computed by means of the semi-empirical MNDO method.

Asymmetric reduction of prochiral ketones using oxazaborolidines has become one of the standard tools for the synthetic chemist, allowing access to enantiomerically enriched secondary alcohols with excellent enantiomeric excess that may seve as the chiral ligands for enantionselectivity synthesis and highly useful intermediates in the sy.