Diastereospecific arylation and cascade deconstructive amidation/thioesterification of readily available lactam-fused bromolactones
Minh Do,
Stella I. Anosike,
Timothy K. Beng
Abstract:Readily available lactam-bromolactones have been interrogated in several fragment growth protocols including diastereospecific Kumada cross-coupling with Grignard reagents, cascade deconstructive amidation, and contra-thermodynamic thioesterification.
The bromoetherification of readily affordable lactam-tethered trisubstituted tertiary alkenols has facilitated the site-selective, efficient, and stereocontrolled synthesis of halogenated fused lactam-tetrahydropyrans.
The bromoetherification of readily affordable lactam-tethered trisubstituted tertiary alkenols has facilitated the site-selective, efficient, and stereocontrolled synthesis of halogenated fused lactam-tetrahydropyrans.
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