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Phenol Oxidative Dearomatization of Modified Nucleoside Templates: A Simple Access to the C7-Spiroannulated Octosyl Acid Framework
Synthesis ( IF 2.2 ) Pub Date : 2017-08-28 , DOI: 10.1055/s-0036-1588543
Chepuri Ramana 1 , Venkannababu Mullapudi 1 , Ravindra Bhogade 1 , Mukund Deshpande 2
Affiliation  

Published as part of the Special Topic Modern Cyclization Strategies in Synthesis

Abstract

Phenol oxidative dearomatization and cyclization has been executed successfully on nucleoside templates to synthesize C7-spiroannulated perhydrofuropyran nucleosides and C6-spiroannulated perhydrofurofuran nucleosides as novel analogues of octosyl acid and related peptidyl nucleosides.

Phenol oxidative dearomatization and cyclization has been executed successfully on nucleoside templates to synthesize C7-spiroannulated perhydrofuropyran nucleosides and C6-spiroannulated perhydrofurofuran nucleosides as novel analogues of octosyl acid and related peptidyl nucleosides.



中文翻译:

修饰的核苷模板的苯酚氧化脱芳香化作用:一个简单的访问C7-Spiroannulated辛基酸框架

作为专题“现代合成中的环化策略”的一部分发布

抽象的

已成功地在核苷模板上进行了酚氧化脱芳香化和环化反应,以合成C7-螺环化的全氢呋喃呋喃核苷和C6-螺环化的全氢呋喃呋喃核苷,作为辛基酸和相关肽基核苷的新型类似物。

已成功地在核苷模板上进行了酚氧化脱芳香化和环化反应,以合成C7-螺环化的全氢呋喃呋喃核苷和C6-螺环化的全氢呋喃呋喃核苷,作为辛基酸和相关肽基核苷的新型类似物。

更新日期:2017-08-28
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