4.4 Article

Organocatalytic regio- and enantioselective vinylogous aza-Morita-Baylis-Hillman reaction

Journal

TETRAHEDRON LETTERS
Volume 115, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2022.154306

Keywords

Asymmetric organocatalysis; Aza-Morita-Baylis-Hillman reaction; Chiral amine; Regioselectivity; 7-Selectivity

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Asymmetric regioselective vinylogous aza-Morita-Baylis-Hillman reactions were conducted using organocatalysis. The reactions between 3-vinylcyclopentenone and various aldimines, in the presence of chiral pyrrolidinopyridine catalysts, yielded 7-adducts with high regioselectivity and moderate enantioselectivity.
Asymmetric regioselective vinylogous aza-Morita-Baylis-Hillman reactions by organocatalysis were developed. The reactions of 3-vinylcyclopentenone with various aldimines in the presence of chiral pyrrolidinopyridine catalysts gave the 7-adducts in high regioselectivity and moderate enantioselectivity.(c) 2022 Elsevier Ltd. All rights reserved.

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