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Curr Top Med Chem ; 13(17): 2099-103, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-23978131

RESUMO

A four-step approach for the synthesis of dihydroxylated piperidine, quinolizidine and indolizidine systems is described employing α,ß-unsaturated diazoketones as versatile building blocks. Unsaturated diazoketones were readily prepared from a Horner-Wadsworth-Emmons reaction between a diazophosphonate and amino-aldehydes. The strategy employs an asymmetric dihydroxylation reaction as the key step and is simple and straightforward enough to be extended to other nitrogen heterocycles.


Assuntos
Compostos de Diazônio/química , Indolizidinas/química , Piperidinas/química , Quinolizidinas/química , Estrutura Molecular , Estereoisomerismo
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