A 13c-n.m.r. study of a di- and a tri-saccharide containing the α-d-galactopyranosyl group
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference21 articles.
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3. Use of positively charged, leaving groups in the synthesis of α-D-linked galactosides. Attempted synthesis of 3-O-α-(D-(galactopyranosyl)-D-galactose
4. Derivatives of 4-Amino-4-deoxy-D-glucose1a
5. Selective acylation of pyranoside—I.
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1. 4,4-(Ethylenedithio)pentanoyl: A masked levulinoyl protective group in the synthesis of oligosaccharides;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
2. Application of levulinic acid ester as a protective group in the synthesis of oligosaccharides;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
3. Iridoid glycosides from Penstemon confertus;Phytochemistry;1987
4. Structure of the d-galacto-d-mannan isolated from the seeds of Melilotus indica All;Carbohydrate Research;1986-09
5. Structural studies on a glycopeptide from the tree fungus Cyttaria harioti Fischer;Carbohydrate Research;1985-05
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