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Org Biomol Chem ; 11(40): 6967-74, 2013 Sep 25.
Artículo en Inglés | MEDLINE | ID: mdl-24057265

RESUMEN

A series of trans- or cis-stilbenes have been synthesized in good to excellent yields via a functional group-dependent decarboxylation process from the corresponding 2,3-diaryl acrylic acids in a neutral CuI/1,10-phen/PEG-400 system under microwave conditions. The in situ generation of the recyclable catalytic complex, the use of environmentally benign solvent PEG-400, the operational simplicity, the short reaction times, as well as the functional group-dependent chemo- and stereo-selectivity have made the decarboxylation process a highly efficient and applicable protocol.


Asunto(s)
Acrilatos/química , Cobre/química , Yoduros/química , Microondas , Fenantrolinas/química , Polietilenglicoles/química , Estilbenos/síntesis química , Catálisis , Descarboxilación , Estructura Molecular , Compuestos Organometálicos/química , Estereoisomerismo , Estilbenos/química
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