Issue 23, 1996

Asymmetric aziridine synthesis via aza-Darzens reaction of bromoacylcamphorsultam

Abstract

The aza-Darzens reaction of the chiral enolate derived from bromoacetylcamphorsultam 1 with N-(diphenyl-phosphinyl)aryl- and tert-butyl-methanimines proceeds in good yield to give cis-N-(diphenylphosphinyl)aziridinylcarbonyl sultams with high de. Monochiral cis-aziridinecarboxylates may be obtained in acceptable yield by hydrolysis of these sultams.

Article information

Article type
Paper

Chem. Commun., 1996, 2631-2632

Asymmetric aziridine synthesis via aza-Darzens reaction of bromoacylcamphorsultam

A. A. Cantrill, L. D. Hall, A. N. Jarvis, H. M. I. Osborn, J. Raphy and J. B. Sweeney, Chem. Commun., 1996, 2631 DOI: 10.1039/CC9960002631

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