NHC-catalyzed enantioselective C2-functionalization of 3-hydroxychromenones via α,β-unsaturated acyl azoliums.

Autor: Dzieszkowski, Krzysztof, Słotwiński, Michał, Rafińska, Katarzyna, Muzioł, Tadeusz M., Rafiński, Zbigniew
Předmět:
Zdroj: Chemical Communications; 10/7/2021, Vol. 57 Issue 78, p9999-10002, 4p
Abstrakt: A novel synthetic method for enantioselective C2-functionalization of 3-hydroxychromenones promoted by N-heterocyclic carbenes via the formation of α,β-unsaturated acyl azolium intermediates, which occurs with Coates–Claisen rearrangement is established. This synthetic strategy enabled the rapid assembly of enantiomerically enriched δ-hydroxychromenone-derived esters/amides under mild conditions with good to excellent yields and broad substrate scope. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index