4.4 Article

Asymmetric Synthesis of Chiral Oxazolines by Organocatalytic Cyclization of α-Aryl Isocyanoesters with Aldehydes

Journal

SYNLETT
Volume -, Issue 13, Pages 2191-2197

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0029-1217549

Keywords

cinchona alkaloid; formal [3+2] cycloaddition; alpha-aryl isocyanoester; aldehydes; chiral oxazolines

Funding

  1. NSFC [20732006]

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A cinchona alkaloid derivative catalyzed the asymmetric formal [3+2] cycloaddition of alpha-aryl isocyanoesters with aldehydes, affording highly substituted 2-oxazolines with good stereoselectivities of up to 18:1 dr and 90% ee.

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