Harnessing the 1,3-azadiene-anhydride reaction for the regioselective and stereocontrolled synthesis of lactam-fused bromotetrahydropyrans by bromoetherification of lactam-tethered trisubstituted tertiary alkenols
Ifeyinwa S. Anosike,
Timothy K. Beng
Abstract:The bromoetherification of readily affordable lactam-tethered trisubstituted tertiary alkenols has facilitated the site-selective, efficient, and stereocontrolled synthesis of halogenated fused lactam-tetrahydropyrans.
Two cascade approaches featuring bromocycloetherification-elimination or dehydrogenative cycloetherification-isomerization of lactam-tethered alkenols have facilitated the stereocontrolled synthesis of lactam-fused 3-methylenetetrahydropyrans.
Two cascade approaches featuring bromocycloetherification-elimination or dehydrogenative cycloetherification-isomerization of lactam-tethered alkenols have facilitated the stereocontrolled synthesis of lactam-fused 3-methylenetetrahydropyrans.
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