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Stereoselective Synthesis of Tri- and Tetrasubstituted Olefins via 1,6-Additions of Diazo Compounds and Their Precursors to p-Quinone Methides
Journal
ACS Organic and Inorganic Au
Date Issued
2021-12-01
Author(s)
Pati, Soumyaranjan
Rayi, Soniya
Namboothiri, Irishi N.N.
Abstract
Reactions of para-quinone methides (p-QMs) with α-diazo-β-ketosulfones and their corresponding esters as well as simple β-dicarbonyl compounds and β-ketosulfones have been carried out under basic conditions. While the reaction of diazosulfone with p-QMs afforded trisubstituted olefins via deacylative 1,6-addition and elimination, α-diazo-β-ketoesters and various active methylene compounds such as 1,3-dicarbonyls and β-ketosulfones afforded tetrasubstituted olefins via 1,6-addition and aerial oxidation. These simple, environmentally benign, and mechanistically diverse protocols provided the products in moderate to excellent yields and selectivities.
Subjects