Synthesis of novel 3′-C-methyl-4′-thio apionucleosides via highly enantioselective elaboration of quaternary carbon by [3,3]-sigmatropic rearrangement-Reference-Cited by-同舟云学术

Synthesis of novel 3′-C-methyl-4′-thio apionucleosides via highly enantioselective elaboration of quaternary carbon by [3,3]-sigmatropic rearrangement

Published:1999-01 Issue:2 Volume:40 Page:231-234
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Hong Joon H.,Gao Mu-Yun,Chu Chung K.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference28 articles.

1. In search of a selective antiviral chemotherapy

2. Current status of anti-HBV chemotherapy

3. Effects of antiviral nucleoside analogs on human DNA polymerases and mitochondrial DNA synthesis

4. Asymmetric synthesis of 1,3-dioxolane-pyrimidine nucleosides and their anti-HIV activity.

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