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Authordc.contributor.authorCassels Niven, Bruce es_CL
Authordc.contributor.authorHerreros, S. es_CL
Authordc.contributor.authorIbáñez, C. es_CL
Authordc.contributor.authorRozende, M. C. es_CL
Authordc.contributor.authorSebastián, C. 
Authordc.contributor.authorSepúlveda, S. es_CL
Admission datedc.date.accessioned2012-08-09T21:32:33Z
Available datedc.date.available2012-08-09T21:32:33Z
Publication datedc.date.issued1981-12
Cita de ítemdc.identifier.citationAnales Asoc. Quím. Argentina , 70, 283-288, 1982.es_CL
Identifierdc.identifier.issn0365-0375
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/119551
Abstractdc.description.abstractl-Aryl-2-nitroalkenes can. ba synthesized mest convéniently by refluxing aromatic aidehydes with nitromethane 01' nitroethane in acetic acid using n-butyla llIineas a catalyst •.{ In this way' seventeen nev cOIIl'PC'lmdosf this type aad seve-raI known ana10gues withalkaxy andhalo ring substituents ware prepared. without the CODcurrent production ol the corref5l'011dingly' substituted benzonitrii_. Moat of thes!! compounds were- tested in theP-J88 murine 1ympbocytic leuk.emia aseay; {QUr of them pc~s_sed reproducible antitumor activity, and another five gav& si~ficantiy increased survival times wtri.ch _re not rept'Oducedes_CL
Patrocinadordc.description.sponsorshipEste trabajo se realizó con el financiamiento de DICYT (USACH).es_CL
Lenguagedc.language.isoeses_CL
Publisherdc.publisherAsoc. Quím. Argentinaes_CL
Títulodc.titleSINTESIS DE 1-ARIL-2-NITROALQUENOS ANTITUMORALESes_CL
Document typedc.typeArtículo de revista


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