Issue 19, 1974

Absolute configurations of some tartaric acid derivatives determined by a key–lock complexation method

Abstract

Absolute configurations of the enantiomers of threo-2-methyltartaric acid and 2,3-dimethyltartaric acid have been determined from stereoselective differences observed in the extent of binding at a chiral vanadyl(IV) site; the method can also rapidly distinguish between erythro and threo isomers and is applicable to other substituted tartaric acids.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1974, 791-792

Absolute configurations of some tartaric acid derivatives determined by a key–lock complexation method

S. K. Hahs and R. E. Tapscott, J. Chem. Soc., Chem. Commun., 1974, 791 DOI: 10.1039/C39740000791

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