Syntheses of L-threose and D-erythrose analogues modified at position 2

C André, J Bolte, C Demuynck

Index: Andre, Corinne; Bolte, Jean; Demuynck, Colette Tetrahedron Asymmetry, 1998 , vol. 9, # 8 p. 1359 - 1367

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Citation Number: 15

Abstract

2-O-Methyl-d-erythrose, 2-O-methyl-l-threose, 2-deoxy-d-and l-erythrose, and the corresponding acetonides have been prepared from the commercially available d- isoascorbic and l-ascorbic acids. The proportion of cyclic (α and β furanoses) and acyclic (aldehyde and hydrate) forms was determined in aqueous (D2O) solution by 1H and 13C NMR spectroscopy.