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Enantioselective synthesis of non-proteinogenic 2-arylallyl-α-amino acids via Pd/In catalytic cascades

By R. Grigg, S. McCaffrey, V. Sridharan, C.W.G. Fishwick, C. Kilner, S. Korn, K. Bailey and J. Blacker

Abstract

An efficient synthesis of both R- and S-enantiomers of 2-arylallyl-α-amino acids via a diastereoselective Pd/In mediated catalytic allylation of chiral N-sulfinyl-α-imino esters is described. The potential for further enhancement of molecular complexity and creating contiguous chiral centres by interfacing these processes with catalytic cyclisation–anion capture methodology is demonstrated. \ud \u

Publisher: Elsevier
Year: 2006
OAI identifier: oai:eprints.whiterose.ac.uk:1939

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