Add to ORKG4-(Methyl, phenyl, benzyl, and i-propyl)-5,5-dimethyl-oxazolidin-2-ones, readily available from α-amino acids, are shown to be effective chiral auxiliaries for stereoselective enolate alkylations and conjugate additions of attached N-acyl moieties. © 1995
N-Acyl-oxazolidinones and enantiomerically pure β-amino alcohol derivatives play an increasingly imp...
The incorporation of a gem-dimethyl group at the 5-position of a chiral oxazolidinone biases the con...
The catalytic enantioselective addition of 2-tert-butyl-4-aryl-1,3-oxazol-5-ones to maleimides is re...
4-(Methyl, phenyl, benzyl, and i-propyl)-5,5-dimethyl-oxazolidin-2-ones, readily available from α-am...
Studies on the alkylation of enolates derived from a range of W-acyl-5,5-dimethyloxazolidin-2-ones a...
Various chiral oxazolidinones (Evans’ oxazolidinones) have been employed as effective chiral auxilia...
Homochiral beta-amino esters ( prepared on multigram scale by lithium amide conjugate addition) are ...
Homochiral beta-amino esters (prepared on multigram scale by lithium amide conjugate addition) are r...
Homochiral beta-amino esters (prepared on multigram scale by lithium amide conjugate addition) are r...
A series of three 5,5-diaryl substituted oxazolidin-2-ones (diphenyl, dinaphthyl and ditolyl) have b...
A series of three 5,5-diaryl substituted oxazolidin-2-ones (diphenyl, dinaphthyl and ditolyl) have b...
A series of three 5,5-diaryl substituted oxazolidin-2-ones (diphenyl, dinaphthyl and ditolyl) have b...
Background: The most frequently used chiral auxiliaries, oxazolidinones (Evans’ oxazolidinones) have...
The incorporation of a gem-dimethyl group at the 5-position of a chiral oxazolidinone biases the con...
Nucleophilic addition of the chiral lithium enolates of (S)-(-)-4-benzyl-2-oxazolidinone acetamide w...
N-Acyl-oxazolidinones and enantiomerically pure β-amino alcohol derivatives play an increasingly imp...
The incorporation of a gem-dimethyl group at the 5-position of a chiral oxazolidinone biases the con...
The catalytic enantioselective addition of 2-tert-butyl-4-aryl-1,3-oxazol-5-ones to maleimides is re...
4-(Methyl, phenyl, benzyl, and i-propyl)-5,5-dimethyl-oxazolidin-2-ones, readily available from α-am...
Studies on the alkylation of enolates derived from a range of W-acyl-5,5-dimethyloxazolidin-2-ones a...
Various chiral oxazolidinones (Evans’ oxazolidinones) have been employed as effective chiral auxilia...
Homochiral beta-amino esters ( prepared on multigram scale by lithium amide conjugate addition) are ...
Homochiral beta-amino esters (prepared on multigram scale by lithium amide conjugate addition) are r...
Homochiral beta-amino esters (prepared on multigram scale by lithium amide conjugate addition) are r...
A series of three 5,5-diaryl substituted oxazolidin-2-ones (diphenyl, dinaphthyl and ditolyl) have b...
A series of three 5,5-diaryl substituted oxazolidin-2-ones (diphenyl, dinaphthyl and ditolyl) have b...
A series of three 5,5-diaryl substituted oxazolidin-2-ones (diphenyl, dinaphthyl and ditolyl) have b...
Background: The most frequently used chiral auxiliaries, oxazolidinones (Evans’ oxazolidinones) have...
The incorporation of a gem-dimethyl group at the 5-position of a chiral oxazolidinone biases the con...
Nucleophilic addition of the chiral lithium enolates of (S)-(-)-4-benzyl-2-oxazolidinone acetamide w...
N-Acyl-oxazolidinones and enantiomerically pure β-amino alcohol derivatives play an increasingly imp...
The incorporation of a gem-dimethyl group at the 5-position of a chiral oxazolidinone biases the con...
The catalytic enantioselective addition of 2-tert-butyl-4-aryl-1,3-oxazol-5-ones to maleimides is re...