Issue 13, 2022

Enantioselective reaction of N-cyano imines: decarboxylative Mannich-type reaction with malonic acid half thioesters

Abstract

The enantioselective reaction of imines bearing a cyano group as an activating group with malonic acid half thioesters gave chiral cyanamide derivatives with high enantioselectivity. The density functional theory (DFT) calculation clarified the stereochemical outcome and importance of the N-cyano group for imines.

Graphical abstract: Enantioselective reaction of N-cyano imines: decarboxylative Mannich-type reaction with malonic acid half thioesters

Supplementary files

Article information

Article type
Communication
Submitted
23 Dec 2021
Accepted
18 Jan 2022
First published
18 Jan 2022

Chem. Commun., 2022,58, 2172-2175

Enantioselective reaction of N-cyano imines: decarboxylative Mannich-type reaction with malonic acid half thioesters

Y. Oyamada, K. Inaba, T. Sasamori and S. Nakamura, Chem. Commun., 2022, 58, 2172 DOI: 10.1039/D1CC07191B

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