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J Org Chem ; 84(2): 1111-1116, 2019 01 18.
Article in English | MEDLINE | ID: mdl-30562463

ABSTRACT

The first total synthesis of paucidirinine (1d), a highly congested aspidofractinine alkaloid containing a special contracted five-membered lactam ring, was achieved in 10 steps with 8% overall yield from commercially available materials. Several key maneuvers, including tandem enamination/[4 + 2] cycloaddition reaction and SmI2-promoted radical cyclization, were featured in this potentially scalable strategy.

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