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Model studies towards the challenging angularly-oxygenated core of several angucyclinones from an oxidative dearomatization strategy†
Silvia Vila-Gisbert,Antonio Urbano,M. Carmen Carreño
Chemical Communications Pub Date : 03/13/2013 00:00:00 , DOI:10.1039/C3CC41221K
Abstract

Up to six differently substituted highly challenging angularly-oxygenated tricyclic core models of natural angucyclinones were stereoselectively synthesized from a common p-quinol intermediate obtained from Oxone-mediated oxidative dearomatization of the corresponding tricyclic phenol.

Graphical abstract: Model studies towards the challenging angularly-oxygenated core of several angucyclinones from an oxidative dearomatization strategy
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