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Monday, 07 February 2011

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Journal Publications

Enantiospecific Formation of 3,6-Dihydro-1H-pyridin-2-ones: Low Pressure Palladium-Catalysed Decarboxylative Carbonylation of 3-Tosyl-5-vinyloxazolidin-2-ones.

Julian G. Knight, Iain M. Lawson and Christopher N. Johnson, Synthesis, 2006, 227.

Abstract: Palladium-catalysed decarboxylative carbonylation of 3-tosyl-5-vinyloxazolidin-2-ones 5 occurs at atmospheric pressure to give 1-tosyl-3,6-dihydro-1H-pyridin-2-ones 6. The reaction proceeds with no loss of enantiopurity and detosylation with sodium naphthalenide gives the title compounds in good yields.

 
 

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