Issue 13, 1994

A dimethyldioxirane-mediated route to enantiomerically pure tricarbonylchromium(0) complexes of ortho-substituted styrenes

Abstract

Dimethyldioxirane oxidation of tricarbonylchromium(0) complexes of a range of ortho-substituted (S)-α-methylbenzyldimethylamines 3af proceeds smoothly to give enantiomerically pure tricarbonylchromium(0) complexes of ortho-substituted styrenes 4afvia chemoselective oxidation of the tertiary amines to their N-oxides and subsequent Cope reactions.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1994, 1569-1570

A dimethyldioxirane-mediated route to enantiomerically pure tricarbonylchromium(0) complexes of ortho-substituted styrenes

P. W. N. Christian, R. Gil, K. Mu<img border="0" src="https://www.rsc.org/images/entities/char_006e_0304.gif" alt="[n with combining macron]" xmlns="http://www.rsc.org/schema/rscart38" />iz-Fernández, S. E. Thomas and A. T. Wierzchleyski, J. Chem. Soc., Chem. Commun., 1994, 1569 DOI: 10.1039/C39940001569

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