On the regioselectivity of the Hanessian–Hullar reaction in 4,6-O-benzylidene protected galactopyranosides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference22 articles.
1. The reaction of O-benzylidene sugars with N-bromosuccinimide
2. Reaction of O-benzylidene sugars with N-bromosuccinimide. II. Scope and synthetic utility in the methyl 4,6-0-benzylidenehexopyranoside series
3. Reaction of O-benzylidene sugars with N-bromosuccinimide. III. Applications to the synthesis of aminodeoxy and deoxy sugars of biological importance
4. Facile bromination by N-bromosuccinimide of benzylidene acetals of carbohydrates. Application to the synthesis of 2,6-imino carbohydrates (substituted 2,5-oxazabicyclo[2.2.2] octanes)
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2. Hanessian-Hullar reaction in the synthesis of highly substituted trans-3,4-dihydroxypyrrolidines: Rhamnulose iminosugar mimics inhibit α-glucosidase;Tetrahedron;2020-01
3. Synthesis of D-FucNAc-D-ManNAcA Disaccharides Based On the Capsular Polysaccharides Staphylococcus aureus Type 5 and 8;The Journal of Organic Chemistry;2018-12-14
4. Regioselective Ring Opening of 1,3-Dioxane-Type Acetals in Carbohydrates;European Journal of Organic Chemistry;2018-11-27
5. “One-Pot” Protection, Glycosylation, and Protection–Glycosylation Strategies of Carbohydrates;Chemical Reviews;2018-06-05
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