Various chiral oxazolidinones (Evans' oxazolidinones) have been employed as effective
chiral auxiliaries in the asymmetric alkylation of different enolates. This strategy has been …

Asymmetric aldol reactions of oxazolidinones as chiral auxiliaries have been achieved and
attracted significant consideration as one of the most powerful synthetic tools for the carbon …

Cheap transition metal Ni-catalyzed asymmetric hydrogenation of 2-oxazolones was
successfully developed, which provided an efficient synthetic strategy to prepare various …

We report a tandem asymmetric aldehyde–alkyne–amine (A3) coupling-carboxylative
cyclization sequence for the highly enantioselective synthesis of chiral N-aryl 2 …

C-5-substituted triazole-oxazolidinones were synthesized using a bromide catalyzed
cycloaddition between aryl isocyanates and epibromohydrin followed by a three-component …

It has been found for the first time at room temperature that the reaction of an unactivated 2-
alkyl or 2-aryl aziridine with carbon dioxide to generate the corresponding oxazolidinone …

The use of bismuth (III) salts in organic synthesis has attracted an increasing interest over
the last years. Systems comprising of bismuth (III) salts are generally catalytic and involve a …

Although the asymmetric catalysis has made a spurt of progress, the use of chiral auxiliaries
remains crucial in asymmetric synthesis due to both the reliability and versatility of the …

An electrostatically enhanced phenol is utilized as a straightforward, sustainable, and potent
one-component organocatalyst for the atom-economic transformation of epoxides to …

N-Mesyloxycarbamates undergo intramolecular C–H amination reactions to afford
oxazolidinones in good to excellent yields in the presence of rhodium (II) carboxylate …