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Merck

Total synthesis of kopsinine.

Organic letters (2013-02-09)
Jian Xie, Amanda L Wolfe, Dale L Boger
RESUMEN

The use of a powerful intramolecular [4 + 2]/[3 + 2] cycloaddition cascade of an 1,3,4-oxadiazole in the divergent total synthesis of kopsinine (1), featuring an additional unique SmI(2)-promoted transannular cyclization reaction for formation of the bicyclo[2.2.2]octane central to its hexacyclic ring system, is detailed.

MATERIALES
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Sigma-Aldrich
Octane, reagent grade, 98%
Sigma-Aldrich
Octane, anhydrous, ≥99%
Sigma-Aldrich
Octane, electronic grade, ≥99.999% metals basis, ≥99% (CP)
Supelco
Octane, analytical standard