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Authordc.contributor.authorPessoa Mahana, Hernán es_CL
Authordc.contributor.authorAstudillo, C. I. es_CL
Authordc.contributor.authorAraya Maturana, Ramiro 
Admission datedc.date.accessioned2010-06-01T20:03:35Z
Available datedc.date.available2010-06-01T20:03:35Z
Publication datedc.date.issued2002
Cita de ítemdc.identifier.citationSYNTHETIC COMMUNICATIONS 32(9): 1437-1445en_US
Identifierdc.identifier.issn0039-7911
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/120950
Abstractdc.description.abstractSyntheses of new morpholinomethylbenzamides 6 bearing both electron-withdrawing and electron-releasing groups at the aromatic ring are described. The strategy involved synthesis of hippuric acid ethyl esters 3, their hydrolysis to hippuric acids 4, subsequent oxidative decarboxylation to acetate 5 and morpholine addition to provide 6.en_US
Lenguagedc.language.isoenen_US
Publisherdc.publisherMARCEL DEKKER INCen_US
Keywordsdc.subjectMoclobemide analogsen_US
Títulodc.titleSynthesis of N-(morpholinomethyl) benzamides as moclobemide analogsen_US
Document typedc.typeArtículo de revista


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