ω-Aldehydo Sugars Prepared by Ninhydrin Oxidation
Author(s) -
Alan R. Gibson,
Laurence D. Melton,
Keith N. Slessor
Publication year - 1974
Publication title -
canadian journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.323
H-Index - 68
eISSN - 1480-3291
pISSN - 0008-4042
DOI - 10.1139/v74-583
Subject(s) - chemistry , ninhydrin , pyranose , oxidative deamination , organic chemistry , deamination , oxime , medicinal chemistry , amino acid , biochemistry , enzyme
The reaction of ninhydrin with 6-amino-6-deoxy-hexopyranosyl sugars has been investigated. 6-Aldehydocyclohexaamylose and 1,2:3,4-di-O-isopropylidene-α-D-galacto-hexodialdo-1,5-pyranose have been prepared by oxidative deamination of 6-amino-deoxycyclohexaamylose and 6-amino-6-deoxy-1,2:3,4-di-O-isopropylidene-α-D-galactopyranose, respectively, using ninhydrin. The preparation of the two aldehydes by the ninhydrin reaction is compared with the method of photolysis of the corresponding azido sugars. The mass spectra of the perdimethylsilyl derivatives of cyclohexaamylose and O-methyl oxime of 6-aldehydocyclohexaamylose have been recorded.
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