Effective Synthesis of Nucleosides Utilizing O-Acetyl-Glycosyl Chlorides as Glycosyl Donors in the Absence of Catalyst: Mechanism Revision and Application to Silyl-Hilbert-Johnson Reaction-Reference-Cited by-同舟云学术

Effective Synthesis of Nucleosides Utilizing O-Acetyl-Glycosyl Chlorides as Glycosyl Donors in the Absence of Catalyst: Mechanism Revision and Application to Silyl-Hilbert-Johnson Reaction

Published:2017-01-05 Issue:1 Volume:22 Page:84
ISSN:1420-3049
Container-title:Molecules
language:en
Short-container-title:Molecules

Author:

Liang Chengyuan,Ju Weihui,Ding Shunjun,Sun Han,Mao Gennian

Funder

National Natural Science Foundation of China

China Postdoctoral Science Foundation

Publisher

MDPI AG

Subject

Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science

Link

http://www.mdpi.com/1420-3049/22/1/84/pdf

Reference41 articles.

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2. Current Status of Older and New Purine Nucleoside Analogues in the Treatment of Lymphoproliferative Diseases

3. Synthesis of Novel Homo-N-Nucleoside Analogs Composed of a Homo-1,4-Dioxane Sugar Analog and Substituted 1,3,5-Triazine Base Equivalents

4. Enantioselective Synthesis of Homo-N-Nucleosides Containing a 1,4-Dioxane Sugar Analog

5. Perspectives in Nucleoside and Nucleic Acid Chemistry;Lin;Molecules,2001

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