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Catalytic alkylation reactions of weakly acidic carbonyl and related compounds using alkenes as electrophiles†
Yasuhiro Yamashita,Ryo Igarashi,Hirotsugu Suzuki,Shū Kobayashi
Organic & Biomolecular Chemistry Pub Date : 06/08/2018 00:00:00 , DOI:10.1039/C8OB00941D
Abstract

Catalytic alkylation reactions of weakly acidic carbonyl and related pronucleophiles such as amides, esters, and sulfonamides with substituted alkenes have been reported. In the presence of a strong Brønsted base catalyst system, potassium hexamethyldisilazide and 18-crown-6 ether, the desired reactions proceeded in high yields at ambient temperature with a wide substrate scope. These are atom-economical catalytic alkylation reactions of carbonyl and related compounds.

Graphical abstract: Catalytic alkylation reactions of weakly acidic carbonyl and related compounds using alkenes as electrophiles
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