A thiourea-oxazoline library with axial chirality: Ligand synthesis and studies of the palladium-catalyzed enantioselective bis(methoxycarbonylation) of terminal olefins

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Abstract

We report herein the synthesis of novel chiral S,N-heterobidentate thiourea-oxazoline ligands and their application to palladium-catalyzed enantioselective bis(methoxycarbonylation)s of terminal olefins under mild conditions. Copper salts were found to play multiple roles in this reaction. Substituted 2- phenylsuccinates were obtained in >90% yield and up to 84% ee under optimized conditions. © 2010 Wiley-VCH Verlag GmbH&Co. KGaA, Weinheim.

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Gao, Y. X., Chang, L., Shi, H., Liang, B., Wongkhan, K., Chaiyaveij, D., … Huanga, Y. (2010). A thiourea-oxazoline library with axial chirality: Ligand synthesis and studies of the palladium-catalyzed enantioselective bis(methoxycarbonylation) of terminal olefins. Advanced Synthesis and Catalysis, 352(11–12), 1955–1966. https://doi.org/10.1002/adsc.201000070

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