Solvent-free microwave-promoted Michael addition of aza-nucleophiles to benzo[b] thiophen-2-yl-2-propenone

dc.creatorPessoa Mahana, Hernán
dc.creatorGonzález, Marcos
dc.creatorGonzález, Marcelo
dc.creatorPessoa, D.
dc.creatorAraya Maturana, Ramiro
dc.creatorRon Higuera, Nadia Betsabé
dc.creatorSaitz Barría, Claudio
dc.date.accessioned2010-06-02T15:19:55Z
dc.date.accessioned2019-04-25T23:29:21Z
dc.date.available2010-06-02T15:19:55Z
dc.date.available2019-04-25T23:29:21Z
dc.date.created2010-06-02T15:19:55Z
dc.date.issued2009
dc.identifierARKIVOC Pages: 316-325 Part: 11
dc.identifier1424-6376
dc.identifierhttp://repositorio.uchile.cl/handle/2250/120959
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/2425313
dc.description.abstractA series of Michael adducts (5-11) have been synthesized with good yields under solvent-free microwave conditions. Aliphatic and aromatic amines utilized as Michael donors reacted with 1-(4,7-dimethoxybenzo[b] thiophen-2-yl)-2-propen-1-one (4), to produce beta-aminoketones and azaheterocyclic compounds of potential biological interest.
dc.languageen
dc.publisherARKAT USA INC
dc.subjectAza-nucleophiles
dc.titleSolvent-free microwave-promoted Michael addition of aza-nucleophiles to benzo[b] thiophen-2-yl-2-propenone
dc.typeArtículos de revistas


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