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2000
Volume 13, Issue 17
  • ISSN: 1568-0266
  • E-ISSN: 1873-4294

Abstract

A four-step approach for the synthesis of dihydroxylated piperidine, quinolizidine and indolizidine systems is described employing α,β-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.

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/content/journals/ctmc/10.2174/15680266113139990145
2013-09-01
2025-07-06
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