Issue 21, 2021

Palladium-catalyzed asymmetric allylic alkylation of 3-aminooxindoles to access chiral homoallylic aminooxindoles

Abstract

An organometal catalytic conversion of 3-aminooxindoles for the diastereo- and enantioselective synthesis of homoallylic aminooxindoles has been described. The asymmetric allylic alkylation of 3-aminooxindoles with allyl carboxylates proceeded smoothly to afford a series of chiral 3-allyl-3-aminooxindoles. This work offers an alternative route to build these scaffolds. The application of this protocol is also highlighted by a significant conversion of products to the potential applicable spiro[indoline-3,2′-pyrrolidin]-2-one derivatives.

Graphical abstract: Palladium-catalyzed asymmetric allylic alkylation of 3-aminooxindoles to access chiral homoallylic aminooxindoles

Supplementary files

Article information

Article type
Paper
Submitted
21 Mar 2021
Accepted
04 May 2021
First published
04 May 2021

Org. Biomol. Chem., 2021,19, 4720-4725

Palladium-catalyzed asymmetric allylic alkylation of 3-aminooxindoles to access chiral homoallylic aminooxindoles

C. Zhang, Y. Wu, B. Cui, L. Li, W. Han, N. Wan and Y. Chen, Org. Biomol. Chem., 2021, 19, 4720 DOI: 10.1039/D1OB00550B

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