Studies on the reactivities of the secondary hydroxyl groups in 1,6-anhydro-4′,6′-o-benzylidene-β-lactose by selective benzoylation
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference18 articles.
1. Synthesis of 1,6-anhydro-6-thio-β-lactose (6-thiolactosan)
2. Syntheses of 6-Acetamido-6-deoxy-lactose Derivatives
3. Chemical modification of lactose. V. Synthesis of 6'-acetamido-6'-deoxy-.ALPHA.-lactose.
4. Chemical Modification of Lactose. IV. Syntheses of Disaccharide Derivatives Predominantly Modified at the C-6 Position in Lactose
5. Chemical Modification of Lactose. III. Syntheses of 4'-Acetamido-4'-deoxy-α-lactose and 6'-Acetamido-6'-deoxy-α-cellobiose
Cited by 12 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. L;Dictionary of Carbohydrates;1998
2. Synthetic glycoconjugates. 3. An efficient synthesis of a glycoprotein model having a Lex-type trisaccharide sequence of tumor-associated carbohydrate antigen;Macromolecules;1994-01
3. Novel 1,6-Anhydro-β-lactose Derivatives for Rapid and Efficient Syntheses of Oligosaccharide Sequences Containing N-Acetyllactosamine;Chemistry Letters;1992-08
4. Novel Partial Protections of 1, 6–Anhtdro–β-Lactose;Journal of Carbohydrate Chemistry;1990-01
5. Carbohydrates;Carbohydrates;1987
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