Nucleophilic displacements of methyl 2,3-O-isopropylidene-4-O-toluene-p-sulphonyl-α-d-lyxo- and -β-l-ribo-pyranosides, and deamination of the corresponding 4-amino sugars-Reference-Cited by-同舟云学术

Nucleophilic displacements of methyl 2,3-O-isopropylidene-4-O-toluene-p-sulphonyl-α-d-lyxo- and -β-l-ribo-pyranosides, and deamination of the corresponding 4-amino sugars

Published:1976-12 Issue:1 Volume:52 Page:31-47
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Brimacombe John S.,Minshall Jonathan,Tucker Leslie C.N.

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference29 articles.

1. Identification and synthesis of vinelose

2. Nucleophilic displacement reactions in carbohydrates. Part XXII. Formation of 1,4-anhydropyranoses from 1-O-acetyl-6-deoxy-2,3-O-isopropylidene-4-O-methylsulphonyl-α-L-manno- and -talo-pyranose with sodium azide

3. The deamination of methyl 4-amino-4,6-dideoxy-2,3-O-isopropylidene-α-L-talo- and -manno-pyranosides with nitrous acid

4. Mechanism in carbohydrate chemistry

5. New Rearrangements of Hexose 4- and 5-O-Sulfonates

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