4.4 Article

Diastereoselective synthesis of beta-amino ketone and acid derivatives by palladium-catalyzed conjugate addition

Journal

TETRAHEDRON LETTERS
Volume 59, Issue 28, Pages 2736-2740

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2018.05.080

Keywords

Diastereoselective synthesis; beta-Amino ketone; beta-Amino acid; Palladium-catalyzed

Funding

  1. National Natural Science Foundation of China [21172200, 21702191]

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The first diastereoselective synthesis of beta-amino ketone and beta-amino acid derivatives by palladium-catalyzed conjugate addition of arylboronic acids to chiral beta-enamino ketones and beta-enamino esters is reported. The catalytic system employing (S)-4-(tert-butyl)oxazolidin-2-one as the chiral auxiliary in water under an air atmosphere provides beta-amino ketone and beta-amino acid derivatives in high yields with excellent diastereoselectivity. (C) 2018 Elsevier Ltd. All rights reserved.

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