Issue 18, 1974
From the journal:

Journal of the Chemical Society, Chemical Communications

Synthesis and stereochemical correlation of acyclic sugar nucleoside analogues: X-ray crystal structure of (1R)-2,3,4,5-tetra-O-acetyl-1-S-ethyl-1-(1,6-dihydro-6-thioxopurin-9-yl)-1-thio-D-arabinitol

David C. Baker,   Arnaud Ducruix,   Derek Horton  and  Claudine Pascard-Billy  

Abstract

A crystal structure determination has been used to establish the absolute stereochemistry of a mixed acetal derivative, a nucleoside analogue (1) having purine-6-thione (‘6-mercaptopurine’) attached to an acyclic D-arabinose derivative.

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Article information

DOI
https://doi.org/10.1039/C39740000729
Article type
Paper

J. Chem. Soc., Chem. Commun., 1974, 729-730

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Synthesis and stereochemical correlation of acyclic sugar nucleoside analogues: X-ray crystal structure of (1R)-2,3,4,5-tetra-O-acetyl-1-S-ethyl-1-(1,6-dihydro-6-thioxopurin-9-yl)-1-thio-D-arabinitol

D. C. Baker, A. Ducruix, D. Horton and C. Pascard-Billy, J. Chem. Soc., Chem. Commun., 1974, 729 DOI: 10.1039/C39740000729

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