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Please use this identifier to cite or link to this item: http://dspace.library.iitb.ac.in/jspui/handle/10054/12398

Title: Cycloaddition of cyclohexa-2,4-dienones with nitroolefins: An unusual regioselectivity and expeditious entry into nitro-bicyclo[2.2.2]octenones
Authors: SINGH, V
SINGH, RB
TOSH, DK
MOBIN, SM
Keywords: diels-alder reactions
masked o-benzoquinones
organic-synthesis
route
Issue Date: 2008
Publisher: TAYLOR & FRANCIS INC
Citation: SYNTHETIC COMMUNICATIONS, 38(18), 3112-3120
Abstract: Cycloaddition of electron-deficient cyclohexa-2,4-dienones with nitroolefins leading to functionalized bicyclo[2.2.2]octenones with nitro groups is reported. A highly unusual regioselectivity was observed. Crystal structure of one of adducts has also been reported.
URI: http://dx.doi.org/10.1080/00397910802054263
http://dspace.library.iitb.ac.in/xmlui/handle/10054/12398
http://hdl.handle.net/10054/12398
ISSN: 0039-7911
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