Chiral synthons for CARBA-β-D-ribonucleosides. Synthesis of CARBA-4- deoxypyrazofurin and isomeric CARBA-4-deaza-oxoformycin analogues

Article abstract of DOI:10.1080/15257779908043088

Multi-step transformation of enantiomerically pure synthons, (1S,2S,3R,4R)-(4-hydroxymethyl-2,3-isopropylidenedioxy-1-cyclopentyl) methyl butyrate {(-)-5} and (1R,5R,6R,7S)-6,7-(isopropylidenedioxy)-3- oxabicyclo[3.2.1]octane-2-one {(+)-11} into carba-4-deoxypyrazofurin 1 and isomeric carba-4-deaza-oxoformycin 2 analogues is presented.

Full text of DOI:10.1080/15257779908043088

Nucleosides and Nucleotides
ISSN: 0732-8311 (Print) (Online) Journal homepage: http://www.tandfonline.com/loi/lncn19
Chiral Synthons for CARBA-β-D-Ribonucleosides.
Synthesis of CARBA-4-Deoxypyrazofurin and
Isomeric CARBA-4-Deaza-oxoformycin Analogues
Barbara Mohar & Jože Kobe
To cite this article: Barbara Mohar & Jože Kobe (1999) Chiral Synthons for CARBA-β-
D-Ribonucleosides. Synthesis of CARBA-4-Deoxypyrazofurin and Isomeric CARBA-4-
Deaza-oxoformycin Analogues, Nucleosides and Nucleotides, 18:3, 443-456, DOI:
10.1080/15257779908043088
To link to this article: http://dx.doi.org/10.1080/15257779908043088
Published online: 04 Oct 2006.
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Date: 27 March 2016, At: 23:43