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Please use this identifier to cite or link to this item: http://dspace.library.iitb.ac.in/jspui/handle/10054/10688

Title: Cycloaddition of annulated cyclohexa-2,4-dienones and novel reduction of halogen at bridgehead: an expedient route to tetracyclo[6.5.2.0(2,7).0(9,13)]pentadec-2(7),11-dien-14-one and framework of conidiogenol and conidiogenone
Authors: SINGH, V
SINGH, RB
MOBIN, SM
Keywords: lycopodium alkaloids
organic-synthesis
(+)-magellaninone
(-)-magellanine
magellanine
diterpenes
phenols
Issue Date: 2009
Publisher: PERGAMON-ELSEVIER SCIENCE LTD
Citation: TETRAHEDRON, 65(38), 7969-7974
Abstract: An expedient route to tetracyclo[6.5.2.0(2,7).0(9,13)]pentadec-2(7),11-dien-14-one and tetracyclic framework of conidiogenol have been reported. Cycloaddition of annulated cyclohexa-2,4-dienone with cyclopentadiene, photochemical oxa-di-pi-methane reaction and a highly unusual dehalogenation of bridgehead halogen are the key features of our methodology. (C) 2009
URI: http://dx.doi.org/10.1016/j.tet.2009.07.051
http://dspace.library.iitb.ac.in/xmlui/handle/10054/10688
http://hdl.handle.net/10054/10688
ISSN: 0040-4020
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