Epimerization during the acetolysis of 3-O-acetyl-5-O-benzoyl-1,2-O-isopropylidene-3-C-methyl-α-d-ribofuranose. Synthesis of 3′-C-methylnucleosides with the β-d-ribo- and α-d-arabino configurations-Reference-Cited by-同舟云学术

Epimerization during the acetolysis of 3-O-acetyl-5-O-benzoyl-1,2-O-isopropylidene-3-C-methyl-α-d-ribofuranose. Synthesis of 3′-C-methylnucleosides with the β-d-ribo- and α-d-arabino configurations

Published:1988-10 Issue: Volume:181 Page:77-88
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Beigelman Leon N.,Gurskaya Galina V.,Tsapkina Elena N.,Mikhailov Sergey N.

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference22 articles.

1. Branched-chain sugar nucleosides. Synthesis of 3′-C-ethyl (and 3′-C-butyl)uridine

2. Synthesis and properties of 3′-C-methylnucleosides and their phosphoric esters

3. Branched-chain sugar nucleosides. III. 3'-C-methyladenosine

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