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

Authordc.contributor.authorPessoa Mahana, Hernán es_CL
Authordc.contributor.authorGonzález, Marcos es_CL
Authordc.contributor.authorGonzález, Marcelo es_CL
Authordc.contributor.authorPessoa, D. es_CL
Authordc.contributor.authorAraya Maturana, Ramiro es_CL
Authordc.contributor.authorRon Higuera, Nadia Betsabé es_CL
Authordc.contributor.authorSaitz Barría, Claudio 
Admission datedc.date.accessioned2010-06-01T18:57:05Z
Available datedc.date.available2010-06-01T18:57:05Z
Publication datedc.date.issued2009
Cita de ítemdc.identifier.citationARKIVOC Pages: 316-325 Part: 11en_US
Identifierdc.identifier.issn1424-6376
Identifierdc.identifier.urihttp://repositorio.uchile.cl/handle/2250/120943
Abstractdc.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.en_US
Lenguagedc.language.isoenen_US
Publisherdc.publisherARKAT USA INCen_US
Keywordsdc.subjectAza-nucleophilesen_US
Títulodc.titleSolvent-free microwave-promoted Michael addition of aza-nucleophiles to benzo[b] thiophen-2-yl-2-propenoneen_US
Document typedc.typeArtículo de revistaen_US


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