Diels-Alder routes to Prosopis alkaloids
This thesis describes the investigation of the Diels-Alder reaction of the imine (140) with the diene (141) to give four products (142,143,156, 157). At low temperatures the enone (156) is the major product while at ambient temperature the bicyclic compounds (142) and (143) predominate. The reaction...
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University of Cambridge
1987
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| Online Access: | https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.233716 |