Authentic standards for the reductive-cleavage method. The positional isomers of partially methylated and acetylated or benzoylated 1,4-anhydro-d-xylitol

Abstract Described herein is a general method for the synthesis of all positional isomers of methylated and acetylated or benzoylated 1,4-anhydro- d -xylitol. The benzoates are generated simultaneously from 1,4-anhydro- d -xylitol by sequential partial methylation and benzoylation or sequential partial benzoylation and methylation. The individual isomers are obtained in pure form by high-performance liquid chromatography. Debenzoylation and acetylation provided the corresponding acetates. The 1 H NMR spectra of the benzoates and the electron ionization mass spectra of the acetates and the tri- O -methyl derivative are reported herein as are the linear temperature programmed gas-liquid chromatography retention indices of the acetates and the tri- O -methyl derivative on three different capillary columns.