This article describes synthetic studies that culminated in the first total synthesis of the Lycopodium alkaloid sieboldine A. During this study, a number of pinacol-terminated cationic cyclizations were examined to form the cis-hydrindanone core of sieboldine A. Of these, a mild Au (I)-promoted 1, 6-enyne cyclization that was terminated by a semipinacol rearrangement proved to be most efficient. Fashioning the unprecedented N- ...
[Sebesta, David P.; O'Rourke, Sarah S.; Martinez, Rogelio L.; Pieken, Wolfgang A.; McGee, Danny P. C. Tetrahedron, 1996 , vol. 52, # 46 p. 14385 - 14402]