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Total diastereofacial selective iodofunctionalization of terpene derivatives based on Ipy2BF4.

The Journal of organic chemistry (2003-08-16)
José Barluenga, Mónica Alvarez-Pérez, Félix Rodríguez, Fracisco J Fañanás, José A Cuesta, Santiago García-Granda
RESUMEN

Acetonides 1, easily obtained from simple terpenes, react with bispyridine iodonium (I) tetrafluoroborate (Ipy(2)BF(4)) and tetrafluoroboric acid in the presence of nucleophiles to give the corresponding adducts 2 with complete regio and diastereofacial control. Acetonides 1 containing a properly located phenyl or benzyloxy group easily undergo iodocyclization to furnish compounds 3 and 4.

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Sigma-Aldrich
Bis(pyridine)iodonium tetrafluoroborate