摘要:
A method for separation of enantiomers of a lactam represented by formula (I): where n and m are each, independently, 0, 1, 2, or 3; P is H or an N-protecting group; and the dotted line represents an optional double bond, by liquid chromatographing the mixture on a chiral stationary phase, where said stationary phase is derivitized with at least one sugar derivative, with an eluent which comprises acetonitrile.
摘要:
Chiral selectors having α-unsubstituted β-amino acid derivatives of the structure: a stationary phase for separating substance mixtures containing the chiral selector, and processes for separating mixtures of chiral substances, including enantiomers, and especially enantiomers of substances selected from β-amino acids and derivatives thereof, α-amino acids and α-hydroxy acids are provided.
摘要:
Chiral selectors having α-unsubstituted β-amino acid derivatives of the structure: a stationary phase for separating substance mixtures containing the chiral selector, and processes for separating mixtures of chiral substances, including enantiomers, and especially enantiomers of substances selected from β-amino acids and derivatives thereof, α-amino acids and α-hydroxy acids are provided.
摘要:
Chiral selectors having α-unsubstituted β-amino acid derivatives of the structure: a stationary phase for separating substance mixtures containing the chiral selector, and processes for separating mixtures of chiral substances, including enantiomers, and especially enantiomers of substances selected from β-amino acids and derivatives thereof, α-amino acids and α-hydroxy acids are provided.
摘要:
Chiral selectors having α-unsubstituted β-amino acid derivatives of the structure: a stationary phase for separating substance mixtures containing the chiral selector, and processes for separating mixtures of chiral substances, including enantiomers, and especially enantiomers of substances selected from β-amino acids and derivatives thereof, α-amino acids and α-hydroxy acids are provided.
摘要:
Method for the conversion of the enantiomers of .alpha.-lipoic acid into the corresponding racemic mixture by racemizing the .alpha.-lipoic acid (pure optical isomers of .alpha.-lipoic acid or mixtures of optical isomers of .alpha.-lipoic acid wherein one of the optical isomers is present in excess) at temperatures of between 110.degree. C. and 200.degree. C. at pressures of from normal pressure up to 50 bar for a reaction time of 10 to 48 hours.