THE CHEMISTRY OF D-APIOSE: PART II. THE CONFIGURATION OF D-APIOSE IN APIIN

Abstract
The tri-O-methyl-D-apiose derivative obtained from the hydrolysis products of methylated apiin was found to be identical with 2,3,4-tri-O-methyl-D-apio-D-furanose prepared synthetically. Periodate oxidation studies support the suggested cis relationship of the hydroxyl groups at C2 and C3 of the apiose moiety in apiin, and consideration of optical rotation data suggest that a β-type linkage unites the D-apiosyl unit to C2 of the D-glucopyranose residue in apiin.

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