Molecular complexity from aromatics: Synthesis and photoreaction of endo-tricyclo[5.2.2.0(2,6)]undecane - A stereoselective route to tricyclic framework of protoilludanes
DSpace at IIT Bombay
View Archive InfoField | Value | |
Title |
Molecular complexity from aromatics: Synthesis and photoreaction of endo-tricyclo[5.2.2.0(2,6)]undecane - A stereoselective route to tricyclic framework of protoilludanes
|
|
Creator |
SINGH, V
LAHIRI, S PAL, S |
|
Subject |
natural sesquiterpenoids
laurilia-tsugicola metabolites illudol cycloaddition photochemical 1,3-acyl shift |
|
Description |
A stereoselective route towards protoilludanoids from simple aromatic precursor is described. The methodology involves in situ generation of spiroepoxycyclohexadienone and cycloaddition with cyclopentadiene and photochemical 1,3-acyl shift. (c) 2005
|
|
Publisher |
PERGAMON-ELSEVIER SCIENCE LTD
|
|
Date |
2011-08-25T14:38:39Z
2011-12-26T12:57:07Z 2011-12-27T05:46:55Z 2011-08-25T14:38:39Z 2011-12-26T12:57:07Z 2011-12-27T05:46:55Z 2005 |
|
Type |
Article
|
|
Identifier |
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 15(19), 4367-4369
0960-894X http://dx.doi.org/10.1016/j.bmcl.2005.06.030 http://dspace.library.iitb.ac.in/xmlui/handle/10054/11051 http://hdl.handle.net/10054/11051 |
|
Language |
en
|
|