Synthesis of substituted 8-aminoquinolines and phenanthrolines through a Povarov approach
Data(s) |
2011
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Resumo |
The synthesis of 8-aminoquinolines and 1,10-phenanthrolines with substituents in alpha of the nitrogen has been performed through an inverse-demanding aza-Diels-Alder (Povarov reaction) in the fluoroalcohols TFE or HFIP. This path involves simple starting materials: 1,2-phenylenediamines, enol ethers and aldehydes. |
Formato |
application/pdf |
Identificador |
http://eprints.iisc.ernet.in/35795/1/Amino.pdf De, Kavita and Legros, Julien and Crousse, Benoit and Chandrasekaran, Srinivasan and Bonnet-Delpona, Daniele (2011) Synthesis of substituted 8-aminoquinolines and phenanthrolines through a Povarov approach. In: Organic and Biomolecular Chemistry, 9 (2). pp. 347-350. |
Publicador |
Royal Society of Chemistry |
Relação |
http://pubs.rsc.org/en/Content/ArticleLanding/2011/OB/c0ob00496k http://eprints.iisc.ernet.in/35795/ |
Palavras-Chave | #Organic Chemistry |
Tipo |
Journal Article PeerReviewed |