Chemical modification of the nonreducing, terminal group of maltotriose
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference12 articles.
1. Synthesis of 1,6-anhydro-1(6)-thio-β-maltotriose
2. Synthesis of methyl α- and β-maltotriosides and aryl β-maltotriosides
3. Chemical Modification of Maltotriose
4. Chemical modification of trehalose. Part II. Synthesis of the galacto-analogue of trehalose
5. The synthesis of 6-O-(2-acetamido-2-deoxy-β-D-galactopyranosyl)-D-galactose by inversion of configuration
Cited by 17 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. D;Dictionary of Carbohydrates;1998
2. Synthesis of [6″-3H]-, (6″-2H)- and (2-2H)-maltotriose;Carbohydrate Research;1996-01
3. Molecular and crystal structures of two 1,6-anhydro-β-maltotriose derivatives;Carbohydrate Research;1995-12
4. Chemoenzymatic synthesis of 6ω-S-α-d-glucopyranosyl-6ω-thiomaltooligosaccharides: their binding to Aspergillus niger glucoamylase G1 and its starch-binding domain;Carbohydrate Research;1995-11
5. Cyclic dimerization of 1,2-unsaturated maltotriose derivatives with iodinium addition; one-pot preparation of a fully methylated 2 A ,2 D -dideoxy-2 A ,2 D -diiodocyclohexasaccharide;Journal of the Chemical Society, Chemical Communications;1993
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