Volume 24, Issue 32
Natural Products
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ChemInform Abstract: Synthesis of 2′-Deoxy-2′-spirocyclopropyl Cytidine as Potential Inhibitor of Ribonucleotide Diphosphate Reductase.

S. CZERNECKI

S. CZERNECKI

Lab. Chim. Glucides, Univ. Pierre et Marie Curie, F-75005 Paris, Fr.

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L. MULARD

L. MULARD

Lab. Chim. Glucides, Univ. Pierre et Marie Curie, F-75005 Paris, Fr.

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J.-M. VALERY

J.-M. VALERY

Lab. Chim. Glucides, Univ. Pierre et Marie Curie, F-75005 Paris, Fr.

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A. COMMERCON

A. COMMERCON

Lab. Chim. Glucides, Univ. Pierre et Marie Curie, F-75005 Paris, Fr.

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First published: August 10, 1993

Abstract

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ChemInform Abstract

Ribonucleoside diphosphate reductase appears to be a very attractive target for new anticancer agents and research has concentrated on a better understanding of its mechanism of action and the design of selective inhibitors. Based on the mechanism of action of the enzyme, a new class of nucleosides, the title compound (X), which may act as inhibitors is designed. The key step of the synthesis is the condensation with diazomethane giving a (separable) mixture of (VIII) and (IX).

chemical structure image

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