SYNTHESIS OF 2-ARYL-1,3-PROPANEDIAMINES USING A ONE-POT KNOEVENAGEL-MICHAEL SEQUENCE

A simple synthetic route for the preparation of 2-phenyl-1,3-propanediamines, based on a Knoevenagel-Michael double condensation followed by reduction, was developed using nitromethane as reagent and solvent, and sodium bicarbonate as base in the first step, followed by catalytic hydrogenation over...

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Autores principales:	ITURRIAGA-VÁSQUEZ,PATRICIO, LÜHR-SIERRA,SUSAN, CAROLI REZENDE,MARCOS, CASSELS,BRUCE K
Lenguaje:	English
Publicado:	Sociedad Chilena de Química 2006
Materias:	Knoevenagel-Michael double condensation 2-phenyl-1,3-propanediamines catalytic hydrogenation Adams catalyst
Acceso en línea:	http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072006000100006
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spelling	oai:scielo:S0717-970720060001000062006-06-08SYNTHESIS OF 2-ARYL-1,3-PROPANEDIAMINES USING A ONE-POT KNOEVENAGEL-MICHAEL SEQUENCEITURRIAGA-VÁSQUEZ,PATRICIOLÜHR-SIERRA,SUSANCAROLI REZENDE,MARCOSCASSELS,BRUCE K Knoevenagel-Michael double condensation 2-phenyl-1,3-propanediamines catalytic hydrogenation Adams catalyst A simple synthetic route for the preparation of 2-phenyl-1,3-propanediamines, based on a Knoevenagel-Michael double condensation followed by reduction, was developed using nitromethane as reagent and solvent, and sodium bicarbonate as base in the first step, followed by catalytic hydrogenation over Adams catalystinfo:eu-repo/semantics/openAccessSociedad Chilena de QuímicaJournal of the Chilean Chemical Society v.51 n.1 20062006-03-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072006000100006en10.4067/S0717-97072006000100006
institution	Scielo Chile
collection	Scielo Chile
language	English
topic	Knoevenagel-Michael double condensation 2-phenyl-1,3-propanediamines catalytic hydrogenation Adams catalyst
spellingShingle	Knoevenagel-Michael double condensation 2-phenyl-1,3-propanediamines catalytic hydrogenation Adams catalyst ITURRIAGA-VÁSQUEZ,PATRICIO LÜHR-SIERRA,SUSAN CAROLI REZENDE,MARCOS CASSELS,BRUCE K SYNTHESIS OF 2-ARYL-1,3-PROPANEDIAMINES USING A ONE-POT KNOEVENAGEL-MICHAEL SEQUENCE
description	A simple synthetic route for the preparation of 2-phenyl-1,3-propanediamines, based on a Knoevenagel-Michael double condensation followed by reduction, was developed using nitromethane as reagent and solvent, and sodium bicarbonate as base in the first step, followed by catalytic hydrogenation over Adams catalyst
author	ITURRIAGA-VÁSQUEZ,PATRICIO LÜHR-SIERRA,SUSAN CAROLI REZENDE,MARCOS CASSELS,BRUCE K
author_facet	ITURRIAGA-VÁSQUEZ,PATRICIO LÜHR-SIERRA,SUSAN CAROLI REZENDE,MARCOS CASSELS,BRUCE K
author_sort	ITURRIAGA-VÁSQUEZ,PATRICIO
title	SYNTHESIS OF 2-ARYL-1,3-PROPANEDIAMINES USING A ONE-POT KNOEVENAGEL-MICHAEL SEQUENCE
title_short	SYNTHESIS OF 2-ARYL-1,3-PROPANEDIAMINES USING A ONE-POT KNOEVENAGEL-MICHAEL SEQUENCE
title_full	SYNTHESIS OF 2-ARYL-1,3-PROPANEDIAMINES USING A ONE-POT KNOEVENAGEL-MICHAEL SEQUENCE
title_fullStr	SYNTHESIS OF 2-ARYL-1,3-PROPANEDIAMINES USING A ONE-POT KNOEVENAGEL-MICHAEL SEQUENCE
title_full_unstemmed	SYNTHESIS OF 2-ARYL-1,3-PROPANEDIAMINES USING A ONE-POT KNOEVENAGEL-MICHAEL SEQUENCE
title_sort	synthesis of 2-aryl-1,3-propanediamines using a one-pot knoevenagel-michael sequence
publisher	Sociedad Chilena de Química
publishDate	2006
url	http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072006000100006
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SYNTHESIS OF 2-ARYL-1,3-PROPANEDIAMINES USING A ONE-POT KNOEVENAGEL-MICHAEL SEQUENCE

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