Synthesis of derivatives of methyl β-maltotrioside
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference15 articles.
1. Chemical modification of the nonreducing, terminal group of maltotriose
2. Synthesis of methyl α- and β-maltotriosides and aryl β-maltotriosides
3. Synthesis of 1,6-anhydro-1(6)-thio-β-maltotriose
4. Chemical modification of trehalose. Part VI. The synthesis of analogues containing 2,2′-dideoxy-functions
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1. Efficient regioselective chemical modifications of maltotriose: an easy access to oligosaccharidic scaffold;Carbohydrate Research;2008-11
2. A simple preparation of α- and β-nigerose octaacetate and β-nigerotriose hendecaacetate by the acetolysis of an alkali-soluble d-glucan from the fruit body of Laetiporus sulphureus;Carbohydrate Research;1983-03
3. A convenient synthesis of laminarabiose and some of its glycosides;Carbohydrate Research;1979-12
4. The koenigs-knorr reaction of methyl 4,6-O-benzylidene-β-D-glucopyranoside with 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide;Carbohydrate Research;1979-12
5. Partial benzoylation of methyl α-sophoroside and methyl α-laminarabioside;Carbohydrate Research;1979-03
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