Issue 3, 2024

Organocatalytic enantioselective Mannich and retro-Mannich reactions and combinations of these reactions to afford tetrasubstituted α-amino acid derivatives

Abstract

Organocatalytic asymmetric Mannich reactions and kinetic resolutions of the products via retro-Mannich reactions that afford enantiomerically enriched tetrasubstituted α-amino acid derivatives (α,α-disubstituted-α-amino acid derivatives) were developed. Furthermore, the combination of the Mannich reaction and the retro-Mannich reaction allowed access to products with almost perfect enantiopurities.

Graphical abstract: Organocatalytic enantioselective Mannich and retro-Mannich reactions and combinations of these reactions to afford tetrasubstituted α-amino acid derivatives

Supplementary files

Article information

Article type
Communication
Submitted
15 Nov 2023
Accepted
30 Nov 2023
First published
15 Dec 2023
This article is Open Access
Creative Commons BY-NC license

Org. Biomol. Chem., 2024,22, 477-481

Organocatalytic enantioselective Mannich and retro-Mannich reactions and combinations of these reactions to afford tetrasubstituted α-amino acid derivatives

K. Chen and F. Tanaka, Org. Biomol. Chem., 2024, 22, 477 DOI: 10.1039/D3OB01855E

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