Expeditious preparation of aristeromycin analogues.: Synthesis of 2′,3′-dideoxyaristeromycin

被引：0

作者：

Comin, MJ ^{[1
]}

Rodriguez, JB ^{[1
]}

机构：

[1] Univ Buenos Aires, Fac Ciencias Exactas & Nat, Dept Quim Organ, RA-1428 Buenos Aires, DF, Argentina

来源：

ANALES DE LA ASOCIACION QUIMICA ARGENTINA | 1998年 / 86卷 / 3-6期

关键词：

D O I：

暂无

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The preparation of the carbocyclic nucleoside 2',3'dideoxyaristeromycin was carried out in ten steps starting from the readily available cyclohex-2-enone. A convergent approach was envisioned using a Mitsunobu metholology as key step to incorporate the heterocyclic base onto the carbocyclic ring.

引用

页码：131 / 138

页数：8

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