An asymmetric tandem reaction of dicyanoalkenes with conjugated sulfinyl imino esters

Abstract

An asymmetric tandem reaction of α,α-dicyanoalkenes and enantiomerically pure α,β-unsaturated N-sulfinyl imino esters is reported herein. It involves a four-step protocol that ends up in the generation of a new family of tetracyclic products in a diastereoselective fashion. The overall process takes place with good yields and moderate to good enantioselectivities, and entails the formation of three bonds and four stereocenters. A plausible reaction mechanism has also been proposed.

Graphical abstract: An asymmetric tandem reaction of dicyanoalkenes with conjugated sulfinyl imino esters

Supplementary files

Article information

Article type
Paper
Submitted
15 Feb 2026
Accepted
16 Mar 2026
First published
16 Mar 2026
This article is Open Access
Creative Commons BY license

Org. Biomol. Chem., 2026, Advance Article

An asymmetric tandem reaction of dicyanoalkenes with conjugated sulfinyl imino esters

F. Ferrer-Pérez, M. Escolano, D. Gaviña, S. Díaz-Oltra, A. Sanz-Marco, M. Sánchez-Roselló and C. del Pozo, Org. Biomol. Chem., 2026, Advance Article , DOI: 10.1039/D6OB00277C

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