Asymmetric Michael-initiated ring closing reactions promoted by hydrogen bonding organocatalysis and the synthesis of cannabinoid metabolites
Hydrogen bonding organocatalysis has been used to develop two novel asymmetric Michael-initiated ring-closing reactions, reported herein. A reaction between vinyl cyanosulfones and bromomalonates, promoted by a novel cupreine organocatalyst, yielded highly substituted cyciopropanes as single diaster...
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University of Reading
2018
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| Online Access: | https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.741110 |