Pd-Catalyzed Cross-Coupling of Cyclopropanols with 2-Br-p-Quinone Methides/2-Br-Cinnamate Esters Followed by a 1,6- and 1,4-Conjugate Addition Reaction

Organic Letters, Journal Year: 2025, Volume and Issue: unknown

Published: March 10, 2025

A novel cascade Pd-catalyzed cross-coupling reaction of cyclopropyl alcohol-derived ketone homoenolate with 2-Br-p-quinone methides and 2-Br-cinnamate esters followed by a 1,6- 1,4-conjugate addition is disclosed. This protocol converts various alcohols into homoenolate, which undergoes C-C bond formation 2-Br p-quinone esters. The salient features this methodology include its operational simplicity, mild conditions, an environmentally benign protocol, high efficiency, good to excellent yields, wide substrate scope.

Language: Английский

Transition-metal-free regioselective synthesis of spiro-oxazolidines through [3 + 2] annulation reactions of azadienes with haloalcohols

RSC Advances, Journal Year: 2025, Volume and Issue: 15(14), P. 10634 - 10638

Published: Jan. 1, 2025

The transition-metal-free regioselective [3 + 2] annulation of azadienes with haloalcohols for the preparation highly functionalized spiro-oxazolidines is experimentally simple, broad substrate scope, good yields, and excellent regioselectivity.

Language: Английский