Specific isotopic labeling of sugars. Specific c-deuteration of 1,6-anhydro-2,3-O-isopropylidene-β-D-talopyranose through enolization of an aldosulose derivative: n.m.r. spectral studies
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference20 articles.
1. Specific labeling of sugars through enolization of aldosulose derivatives. Synthesis of 1,6-anhydro-β-D-talopyranose
2. Enolization of aldosulose derivatives. 4-O-acetyl-1,6-anhydro-2-3-O-isopropylidene-β-D-threo-hex-3-enopyranose, the 3,4-enediol acetate of a fused-ring keto sugar, and formation of a branched-chain sugar derivative
3. 1,6-anhydro-2,3-O-isopropylidene-β-D-lyxo-hexopyranos-4-ulose
4. 1,6-Anhydro-4-deoxy-4-diazo-2,3-O-isopropylidene-β-D-lyxo-hexopyranose, a stable diazo-sugar from a keto-sugar precursor
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2. Intra- and Intermolecular 1,3-Dipolar Cycloaddition of Sugar Ketonitrones with Mono-, Di-, and Trisubstituted Dipolarophiles;The Journal of Organic Chemistry;2003-05-10
3. 4-Amino-4-cyano-4,6-dideoxy sugar derivatives from methyl 6-deoxy-2,3-O-isopropylidene-α-l-lyxo-hexopyranosid-4-ulose via Strecker-type reaction;Carbohydrate Research;1998-09
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5. Synthesis of 1- and 1,2,2'-deuteriated deoxyribose and incorporation into deoxyribonucleosides;The Journal of Organic Chemistry;1991-02
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