A synthetic approach to a novel class of enantiopure cyclopentyl carbocyclic nucleosides and related compounds

Miguel Díaz; Rosa M. Ortuño

doi:10.1016/S0957-4166(97)00401-1

A synthetic approach to a novel class of enantiopure cyclopentyl carbocyclic nucleosides and related compounds

Miguel Díaz, Rosa M. Ortuño

Department of Chemistry

Research output: Contribution to journal › Article › Research › peer-review

5 Citations (Scopus)

Abstract

A Synthetic entry to a novel class of cyclopentyl carbocyclic nucleusides and other functional derivatives, in enantiopure form, is presented. As a structural feature of these compounds, the base-moiety is separated from the carbocyclic ring by a C2-chain containing a quaternary stereogenic center and additional chemical functions.

Original language	English
Pages (from-to)	3421-3430
Journal	Tetrahedron Asymmetry
Volume	8
Issue number	20
DOIs	https://doi.org/10.1016/S0957-4166(97)00401-1
Publication status	Published - 23 Oct 1997

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title = "A synthetic approach to a novel class of enantiopure cyclopentyl carbocyclic nucleosides and related compounds",

abstract = "A Synthetic entry to a novel class of cyclopentyl carbocyclic nucleusides and other functional derivatives, in enantiopure form, is presented. As a structural feature of these compounds, the base-moiety is separated from the carbocyclic ring by a C2-chain containing a quaternary stereogenic center and additional chemical functions.",

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T1 - A synthetic approach to a novel class of enantiopure cyclopentyl carbocyclic nucleosides and related compounds

AU - Díaz, Miguel

AU - Ortuño, Rosa M.

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N2 - A Synthetic entry to a novel class of cyclopentyl carbocyclic nucleusides and other functional derivatives, in enantiopure form, is presented. As a structural feature of these compounds, the base-moiety is separated from the carbocyclic ring by a C2-chain containing a quaternary stereogenic center and additional chemical functions.

AB - A Synthetic entry to a novel class of cyclopentyl carbocyclic nucleusides and other functional derivatives, in enantiopure form, is presented. As a structural feature of these compounds, the base-moiety is separated from the carbocyclic ring by a C2-chain containing a quaternary stereogenic center and additional chemical functions.

U2 - 10.1016/S0957-4166(97)00401-1

DO - 10.1016/S0957-4166(97)00401-1

M3 - Article

VL - 8

SP - 3421

EP - 3430

IS - 20

ER -

A synthetic approach to a novel class of enantiopure cyclopentyl carbocyclic nucleosides and related compounds

Abstract

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