One-pot three component alpha-aminoalkylation of conjugated nitroalkenes and nitrodienes
DSpace at IIT Bombay
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Title |
One-pot three component alpha-aminoalkylation of conjugated nitroalkenes and nitrodienes
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Creator |
RAJESH, K
SHANBHAG, P RAGHAVENDRA, M BHARDWAJ, P NAMBOOTHIRI, INN |
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Subject |
baylis-hillman reaction
methyl vinyl ketone anticancer activity n-sulfinimines cyclic enones lewis base derivatives adducts imidazole aldehydes |
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Description |
Nitroethylenes possessing aryl, heteroaryl, and alkyl substituents at the beta-position as well as delta-substituted nitrobutadienes undergo facile aminoalkylation at the alpha-position upon treatment with formaldehyde and a secondary amine in the presence of imidazole and trifluoroacetic acid to afford alpha-aminoalkylated nitroalkenes and nitrodienes in good to excellent yield and stereoselectivity. (c) 2009
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Publisher |
PERGAMON-ELSEVIER SCIENCE LTD
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Date |
2011-08-25T19:57:36Z
2011-12-26T12:57:12Z 2011-12-27T05:47:08Z 2011-08-25T19:57:36Z 2011-12-26T12:57:12Z 2011-12-27T05:47:08Z 2010 |
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Type |
Article
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Identifier |
TETRAHEDRON LETTERS, 51(5), 846-849
0040-4039 http://dx.doi.org/10.1016/j.tetlet.2009.12.015 http://dspace.library.iitb.ac.in/xmlui/handle/10054/11129 http://hdl.handle.net/10054/11129 |
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Language |
en
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