Journal2025دسترسی آزاد
Regioselective Cu( i )-catalyzed intramolecular hydroacylation and dimerization of propargylarylaldehydes
RSC Advances Vol. 15, No. 52, 44254–44259
چکیده
O salt could promote regioselective intramolecular hydroacylation and head-to-head additive dimerization of propargyl aryl aldehydes in the presence of a catalytic amount of ascorbic acid. The transformations do not require any bases during the course of the reaction. In both transformations, substrates bearing electron-donating groups on the aryl ring are more compatible with the reaction conditions, providing the corresponding coupling products with good yields. In addition, the presented catalytic system shows high regioselectivity control for different substituents regardless of their polarity.
موضوعات و کلیدواژهها
Catalytic Alkyne ReactionsCatalytic C–H Functionalization MethodsSynthesis and Characterization of PyrrolesRegioselectivityHydroacylationIntramolecular forcePropargylArylRing (chemistry)
ارجاع علمی
Zahra Tanbakouchian, Mohammad Ali Zolfigol, Maryam-Sadat Tonekaboni, Anna Kozakiewicz, Rahman Bikas. “Regioselective Cu( i )-catalyzed intramolecular hydroacylation and dimerization of propargylarylaldehydes.” RSC Advances, 2025. https://doi.org/10.1039/d5ra07533e