Stereoselective arylation of pyranoid glycals, using bromomagnesium phenolates: An entry to 2,3-unsaturated C-α-glycopyranosylarenes-Reference-Cited by-同舟云学术

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Stereoselective arylation of pyranoid glycals, using bromomagnesium phenolates: An entry to 2,3-unsaturated C-α-glycopyranosylarenes

Published:1989-08 Issue:2 Volume:191 Page:243-251
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Casiraghi Giovanni,Cornia Mara,Rassu Gloria,Zetta Lucia,Gasparri Fava Giovanna,Ferrari Belicchi Marisa

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference39 articles.

1. 1038. Unsaturated carbohydrates. Part II. Three reactions leading to unsaturated glycopyranosides

2. Unsaturated carbohydrates. Part IX. Synthesis of 2,3-dideoxy-α-D-erythro-hex-2-enopyranosides from tri-O-acetyl-D-glucal

3. A concise and stereoselective route to the predominant stereochemical pattern of the tetrahydropyranoid antibiotics: an application to indanomycin

4. Model studies directed toward the avermectins: A route to the spiroketal subunit

5. Synthesis of a marine polyether toxin, okadaic acid (2) — synthesis of segment b

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3. Newer Synthetic Methods;Green Chemistry and Engineering;2007

4. Strategies towards C-Glycosides;The Organic Chemistry of Sugars;2005-09-21

5. Structure, activity, synthesis and biosynthesis of aryl-C-glycosides;Natural Product Reports;2005

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