Enantioselective Preparation of 2‘,3‘-Dideoxynucleosides and Their Analogues from Ring-Expansion of Cyclobutanones. 2. Synthesis of 2‘,3‘-Dideoxyribosides and (1S,3R)-1- Amino-3-(hydroxymethyl)cyclopentane1-Reference-Cited by-同舟云学术

Enantioselective Preparation of 2‘,3‘-Dideoxynucleosides and Their Analogues from Ring-Expansion of Cyclobutanones. 2. Synthesis of 2‘,3‘-Dideoxyribosides and (1S,3R)-1- Amino-3-(hydroxymethyl)cyclopentane1

Published:1996-01-01 Issue:4 Volume:61 Page:1547-1550
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Lee-Ruff Edward¹,Xi Feng-de¹,Qie Jiang Hua¹

Affiliation:

1. Department of Chemistry, York University, Toronto, Ontario M3J 1P3

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo9517151

Reference29 articles.

1. A Novel Approach toward the Synthesis of Chiral 2,3-Dideoxy Nucleosides and Their Carbocyclic Analogs

2. Synthesis of 2-deoxy-2,2-difluoro-D-ribose and 2-deoxy-2,2'-difluoro-D-ribofuranosyl nucleosides

3. Stereospecific Synthesis of 2-Deoxy-2,2-difluororibonolactone and Its Use in the Preparation of 2′-Deoxy-2′,2′-difluoro-β-D-ribofuranosyl Pyrimidine Nucleosides: The Key Role of Selective Crystallization

4. Robins, R. K.; Revankar, G. R. inAntiviral Drug Development; De Clercq, E., Walker, R. T., Eds.; Plenum Press: New York, 1988; p 11.

5. Molecular Targets for AIDS Therapy

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