A CAN mediated oxidative coupling of 1,3-dicarbonyl compounds to 2-arylchromenes followed by cyclization affords tetrahydro-benzofuro[3,2-c]chromenones with regio- and diastereoselectivity in high yield.
Abstract
A p...
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A Palladium‐Catalyzed Regioselective [3+2] Annulation Strategy to 1,2,3‐Oxathiazolidine‐2‐oxides
European Journal of Organic Chemistry, März 2024, DOI. Login für Volltextzugriff.
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Palladium-catalyzed [3+2] annulation of N-sulfinylanilines with vinylethylene carbonates and vinyl epoxides has been reported, affording the 1,2,3-oxathiazolidine-2-oxides under mild reaction conditions. Further synthetic applications of 1,2,3-oxathiazolidine-2-oxides in the preparation of sulfoxides, β-amino alcohols and amines have also been demonstrated.
Abstract
A palladium-catalyzed [3+2] annulation reaction of N-sulfinylanilines with vinylethylene carbonates and vinyl epoxides is developed. It affords 1,2,3-oxathiazolidine-2-oxides under mild reaction conditions through allylic palladium intermediates. The versatile synthetic utility of 1,2,3-oxathiazolidine-2-oxides in preparing sulfoxides, β-amino alcohols, and substituted amines has also been demonstrated.
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