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
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Creator |
DEB, INDUBHUSAN
JOHN, SUMOD NAMBOOTHIRI, IRISHI NN |
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Subject |
michael addition
nitroaliphatic compounds ring closing metathesis |
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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.
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Publisher |
Elsevier
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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 |
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Type |
Article
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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 |
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Language |
en
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