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Structural diversity through intramolecular cycloaddition and modulation of chemical reactivity in excited state. Synthesis and photoreactions of 3-oxa-tricyclo[5.2.2.01,5]undecenones: novel stereoselective route to oxa-triquinanes and oxa-sterpuranes

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Title Structural diversity through intramolecular cycloaddition and modulation of chemical reactivity in excited state. Synthesis and photoreactions of 3-oxa-tricyclo[5.2.2.01,5]undecenones: novel stereoselective route to oxa-triquinanes and oxa-sterpuranes
 
Creator SINGH, VISHWAKARMA
ALAM, SQ
 
Subject oxa-triquinanes
oxa-sterpuranes
spiroepoxycyclohexa-2,4-dienones
 
Description Synthesis of 11-methyl-3-oxa-tricyclo[5.2.2.01,5]undecenones by intramolecular Diels–Alder reaction of highly labile spiroepoxycyclohexa-2,4-dienones and its photochemical reactions upon triplet (3T) and singlet (1S) excitation leading to a stereoselective route to oxa-triquinane and oxa-sterpurane, respectively, is described.
 
Publisher Elsevier
 
Date 2009-02-20T05:25:50Z
2011-11-25T17:35:00Z
2011-12-26T13:06:29Z
2011-12-27T05:54:19Z
2009-02-20T05:25:50Z
2011-11-25T17:35:00Z
2011-12-26T13:06:29Z
2011-12-27T05:54:19Z
2000
 
Type Article
 
Identifier Bioorganic & Medicinal Chemistry Letters 10(22), 2517-2519
0960-894X
http://dx.doi.org/10.1016/S0960-894X(00)00503-5
http://hdl.handle.net/10054/716
http://dspace.library.iitb.ac.in/xmlui/handle/10054/716
 
Language en