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Synthesis of benzo-fused medium ring cyclic ethers via a Michael addition–ring closing metathesis strategy involving nitroaliphatic compounds

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Title Synthesis of benzo-fused medium ring cyclic ethers via a Michael addition–ring closing metathesis strategy involving nitroaliphatic compounds
 
Creator DEB, INDUBHUSAN
JOHN, SUMOD
NAMBOOTHIRI, IRISHI NN
 
Subject michael addition
nitroaliphatic compounds
ring closing metathesis
 
Description Nitroalkenes derived from O-protected salicylaldehyde undergo facile Michael-type addition of nucleophiles possessing unsaturated tether. Ring closing metathesis of the Michael adducts provides benzo-fused medium ring cyclic ethers possessing a nitroalkyl functionality.
 
Publisher Elsevier
 
Date 2007-12-20T09:11:22Z
2011-11-25T12:19:42Z
2011-12-26T13:08:33Z
2011-12-27T05:56:29Z
2007-12-20T09:11:22Z
2011-11-25T12:19:42Z
2011-12-26T13:08:33Z
2011-12-27T05:56:29Z
2007
 
Type Article
 
Identifier Tetrahedron 63(48), 11991–997
0040-4020
http://dx.doi.org/10.1016/j.tet.2007.09.009
http://hdl.handle.net/10054/60
http://dspace.library.iitb.ac.in/xmlui/handle/10054/60
 
Language en