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Molecular complexity from aromatics: synthesis and photoreaction of endo-tricyclo[5.2.2.02,6]undecane—A stereoselective route to tricyclic framework of protoilludanes

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Title Molecular complexity from aromatics: synthesis and photoreaction of endo-tricyclo[5.2.2.02,6]undecane—A stereoselective route to tricyclic framework of protoilludanes
 
Creator SINGH, VISHWAKARMA
LAHIRI, SANJOY
PAL, SHANTANU
 
Subject 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.
 
Publisher Elsevier
 
Date 2009-02-20T05:25:35Z
2011-11-25T17:34:30Z
2011-12-26T13:06:22Z
2011-12-27T05:54:11Z
2009-02-20T05:25:35Z
2011-11-25T17:34:30Z
2011-12-26T13:06:22Z
2011-12-27T05:54:11Z
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://hdl.handle.net/10054/715
http://dspace.library.iitb.ac.in/xmlui/handle/10054/715
 
Language en