Reaction of Glycosyl Halides with Benzyl Grignard Reagents: Unexpected o-Tolyl Alkylation of Tetra-O-acetylglucopyranosyl Bromide and Direct Synthesis of (B-Glycosyl)phenylmethanes-Reference-Cited by-同舟云学术

Reaction of Glycosyl Halides with Benzyl Grignard Reagents: Unexpected o-Tolyl Alkylation of Tetra-O-acetylglucopyranosyl Bromide and Direct Synthesis of (B-Glycosyl)phenylmethanes

Published:1994-03 Issue:2 Volume:13 Page:293-302
ISSN:0732-8303
Container-title:Journal of Carbohydrate Chemistry
language:en
Short-container-title:Journal of Carbohydrate Chemistry

Author:

Panigot J.¹,Curley W.¹

Affiliation:

1. a Division of Medicinal Chemistry and Pharmacognosy College of Pharmacy , The Ohio State University , Columbus , Ohio , 43210

Publisher

Informa UK Limited

Subject

Organic Chemistry,Biochemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/07328309408009194

Reference31 articles.

1. Synthesis of Naturally Occurring C-Nucleosides, Their Analogs, and Functionalized C-Glycosyl Precursors

2. 1 The Chemistry and Biochemistry of C-Nucleosides and C-Arylglycosides

3. The preparation of C-arylglycals. The palladium-catalyzed coupling of 3,4,6-tri-O-(tert-butyldimethylsilyl)-1-(tributylstannyl)-D-glucal and aryl bromides

4. Preparation of C-aryl glucals via the palladium catalyzed coupling of metalated aromatics with 1-iodo-3,4,6-tri-O-(triisopropylsilyl)-D-glucal

5. C-glycoside synthesis II: Henry condensations of 4,6-O-alkylidene pyranoses with a 1,3-proton transfer catalyst- a route to blocked aminomethyl-C-glycosides.

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