Stereoselective preparations of ribofuranosyl chlorides and ribofuranosyl acetates.Solvent effects and stereoselectivity in the reaction of ribofuranosyl acetates with trimethylallylsilane-Reference-Cited by-同舟云学术

Stereoselective preparations of ribofuranosyl chlorides and ribofuranosyl acetates.Solvent effects and stereoselectivity in the reaction of ribofuranosyl acetates with trimethylallylsilane

Published:1986-01 Issue:9 Volume:27 Page:1011-1014
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Wilcox Craig S.,Otoski Renee M.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference12 articles.

1. A new approach to c-glycoside congeners: Metal carbene mediated methylenation of aldonolactones.

2. Syntheses of γ,δ-unsaturated alcohols from allylsilanes and carbonyl compounds in the presence of titanium tetrachloride

3. Trimethylsilyl trifluoromethanesulfonate as a catalyst of the reaction of allyltrimethylsilane and acetals

4. Electrophilic Substitution of Organosilicon Compounds- Applications to Organic Synthesis

5. Highly stereoselective approaches to .alpha.- and .beta.-C-glycopyranosides

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