Regio- and stereo-specific synthesis of cis-(±)-1-acetoxy-4-(acetoxymethyl)cyclopent-2-ene: a key intermediate in the synthesis of carbocyclic nucleosides and pseudo-ribofuranoses-Reference-Cited by-同舟云学术

Regio- and stereo-specific synthesis of cis-(±)-1-acetoxy-4-(acetoxymethyl)cyclopent-2-ene: a key intermediate in the synthesis of carbocyclic nucleosides and pseudo-ribofuranoses

Published:1993 Issue:14 Volume: Page:1543-1544
ISSN:0300-922X
Container-title:J. Chem. Soc., Perkin Trans. 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Hodgson David M.,Witherington Jason,Moloney Brian A.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1993/P1/P19930001543

Reference5 articles.

1. Synthesis of (±)-2′,3′-didehydro-2′,3′-dideoxy nucleosides via a modified Prins reaction and palladium(0) catalysed coupling

2. Potential use of carbocyclic nucleosides for the treatment of AIDS: chemo-enzymatic syntheses of the enantiomers of carbovir

3. Synthesis of pseudo-ribofuranoses by stereocontrolled reactions on 4-hydroxycyclopent-2-enylmethanol derivatives

4. Improved selectivity in the preparation of some 1,1-difunctionalized 3-cyclopentenes. High yield synthesis of 3-cyclopentenecarboxylic acid

5. Novel Bromolactonization Using a Dimethyl Sulfoxide-Trimethylsilyl Bromide-Amine System; Unusual cis-Addition of trans-6-Substituted 3-Cyclohexene-1-carboxylic Acids

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1. ChemInform Abstract: Regio- and Stereospecific Synthesis of cis-(.+-.)-1-Acetoxy-4-( acetoxymethyl)cyclopent-2-ene: A Key Intermediate in the Synthesis of Carbocyclic Nucleosides and pseudo-Ribofuranoses.;ChemInform;2010-08-20

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