A tandem oxidative dearomatization/intramolecular Diels–Alder reaction: a short and efficient entry into tricyclic system of maoecrystal V
摘要:
A short and efficient route to tricyclic ring system containing bridged bicyclo[2.2.2]octanone annulated with a lactone ring present in the maoecrystal is described. In-situ generation of spiroepoxycyclohexa-2,4-dienone and intramolecular cycloaddition are the key features of our approach. (C) 2010 Elsevier Ltd. All rights reserved.
A tandem oxidative dearomatization/intramolecular Diels–Alder reaction: a short and efficient entry into tricyclic system of maoecrystal V
摘要:
A short and efficient route to tricyclic ring system containing bridged bicyclo[2.2.2]octanone annulated with a lactone ring present in the maoecrystal is described. In-situ generation of spiroepoxycyclohexa-2,4-dienone and intramolecular cycloaddition are the key features of our approach. (C) 2010 Elsevier Ltd. All rights reserved.
A tandem oxidative dearomatization/intramolecular Diels–Alder reaction: a short and efficient entry into tricyclic system of maoecrystal V
作者:Vishwakarma Singh、Pravin Bhalerao、Shaikh M. Mobin
DOI:10.1016/j.tetlet.2010.04.082
日期:2010.6
A short and efficient route to tricyclic ring system containing bridged bicyclo[2.2.2]octanone annulated with a lactone ring present in the maoecrystal is described. In-situ generation of spiroepoxycyclohexa-2,4-dienone and intramolecular cycloaddition are the key features of our approach. (C) 2010 Elsevier Ltd. All rights reserved.