Abstract
Ynamide, is an understudied but attractive class of alkynes, activated by the donating ability of the nitrogen adjacent to alkynes. With the nucleophilicity on β- carbon and the electrophilicity on α-carbon of ynamides, this review summarizes the syntheses of ynamides and miscellaneous reactions - oxidation, rearrangement, cyclization, and cycloaddition to construct complicated heterocyclic rings. The synthetic methodologies were further applied into natural products synthesis, e.g. marinoquinolines A and C, aplidiopsamine A, rigidin A, and 7-azaserotonin derivative.
Keywords: Dipolar Cycloaddition, Haloenamide, Keteniminium, Polycyclic Alkaloids, Thioenamide, Ullmann Coupling, Witulski Rearrangment, α- Ketoimide, Ynamide, Yndiamide.
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