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An efficient synthetic strategy has been developed for annulation of an azocane ring onto a
bicyclo [2.2. 2] octane scaffold via an intramolecular hydroaminomethylation protocol to …

Abstract Oxidative dearomatization of 2-and 4-substituted phenols to their corresponding
benzoquinone monoketals by catalytic amount of iodobenzene, and m-CPBA as a co …

A synthesis of the complete tetracyclic framework of the structurally unique Lycopodium
alkaloid lycopladine H has been accomplished using a strategy involving a double alkene …

A simple and efficient access to highly functionalized isoindolone derivatives via a [3+ 2]
cycloaddition process between in situ generated azomethine ylides with various stable …

We have discovered a highly diastereoselective Michael reaction of α-substituted, β-
nitrocarbonyl compounds to deliver highly functionalized stereodiads containing fully …

Masked o‐benzoquinones, on reaction with nitrile oxides generated in situ from the
corresponding hydroxamoyl chlorides, provide [3+ 2] cycloaddition products or novel …

In work directed toward a total synthesis of the Lycopodium alkaloid lycopladine H (21),
several strategies have been explored based on key tandem oxidative …