Abstract
Ruthenium-catalyzed hydroamidations of alkynes allow a concise
synthetic entry to both E - and Z -configured enamide natural products.
This was demonstrated by the synthesis of botryllamides C and E,
lansiumamides A and B, and lansamide I in 1-3 steps and
57-98% yield from simple, commercially available
precursors.
Key words
alkyne - botryllamide - hydroamidation - lansamide - lansiumamide - ruthenium
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