Issue 36, 2024

Asymmetric synthesis of chiral tricyclic 3,4-dihydropyrimidin-2-thione derivatives catalyzed by chiral imidodiphosphoric acid

Abstract

The asymmetric synthesis of 3,4-dihydropyrimidin-2-(1H)-one thioacetals was achieved for the first time using a chiral imidodiphosphoric acid catalyst. The Biginelli reaction involving aromatic aldehydes, thiourea, and 1,3-cyclohexanedione as a multi-component reaction was conducted in ethyl acetate at 40 °C with a chiral imidodiphosphoric acid catalyst. Under mild conditions, a series of chiral polycyclic 3,4-dihydropyrimidin-2-(1H)-one thioacetals were obtained with high yields and excellent enantioselectivity (up to 99% ee).

Graphical abstract: Asymmetric synthesis of chiral tricyclic 3,4-dihydropyrimidin-2-thione derivatives catalyzed by chiral imidodiphosphoric acid

Supplementary files

Article information

Article type
Paper
Submitted
05 Jul 2024
Accepted
16 Aug 2024
First published
22 Aug 2024

New J. Chem., 2024,48, 15943-15947

Asymmetric synthesis of chiral tricyclic 3,4-dihydropyrimidin-2-thione derivatives catalyzed by chiral imidodiphosphoric acid

L. Kong, P. Wang, C. Ju, G. Zhang and S. Zhang, New J. Chem., 2024, 48, 15943 DOI: 10.1039/D4NJ03039G

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