Stereoselectivity of cycloglycosylation in mannooligose series depends on carbohydrate chain length: Syntheses of manno isomers of β- and γ- cyclodextrins-Reference-Cited by-同舟云学术

Stereoselectivity of cycloglycosylation in mannooligose series depends on carbohydrate chain length: Syntheses of manno isomers of β- and γ- cyclodextrins

Published:1990-01 Issue:22 Volume:31 Page:3191-3194
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Mori Masato,Ito Yukishige,Uzawa Jun,Ogawa Tomoya

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference16 articles.

1. A highly efficient and stereoselective cycloglycosylation. Synthesis of cyclo???→4)-[α-Man-(1→4)]5-α-Man-(1→???, a manno isomer of α-cyclodextrin

2. A highly stereoselective and practical synthesis of cyclomannohexaose, Cyclo{→4)-[α-d-Manp-(1→4)-]5-α-d-Manp-(1→}, a manno isomer of cyclomaltohexaose

3. Benzeneselenenyl triflate as a promoter of thioglycosides : A new method for O-glycosylation using thioglycosides

4. idem., Carbohydr. Res., in press.

5. Complete proton and carbon-13 assignments of coenzyme B12 through the use of new two-dimensional NMR experiments

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