Synthesis of chiral carbocyclic ribonucleotides.

V D Antle, C A Caperelli
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引用次数: 3

Abstract

The carbocyclic analogs of CMP, UMP, GMP, IMP, and ribo-TMP, of the same absolute configuration as the naturally occurring beta-D-ribofuranose-based ribonucleoside monophosphates, have been synthesized. The synthetic route employed Mitsunobu coupling of the heterocycles, appropriately protected where necessary, with a differentially protected, chiral carbocyclic core.

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手性碳环核糖核苷酸的合成。
已经合成了CMP、UMP、GMP、IMP和核糖- tmp的碳环类似物,它们与天然存在的β - d -核呋喃糖基核糖核苷单磷酸具有相同的绝对构型。该合成路线采用杂环的Mitsunobu偶联,在必要时适当地保护,与差异保护的手性碳环核心。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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