Enantioselective synthesis of (-)-meroquinene through tandem Michael reaction methodology

Article abstract of DOI:10.1016/S0040-4020(01)86974-X

An enantioselective approach to the synthesis of non natural (-)-meroquinene 1 based on sequential inter- and intra-molecular Michael reaction between (L)-menthyl N-benzyl-5-amino-2E-pentenoate 3 and 1-acetyloxy-4-methoxymethyloxy-2-nitrobutane 10b, acting as surrogate of 2-nitro-1,3-butadiene 4, is described. The heterocyclization process led to the formation of the piperidine ring system 12, obtained as an unseparable 80:20 mixture of diastereomers at the newly created chiral centres at C-3 and C-4, which became easily separable by column chromatography after transformation of the nitrogen protective benzyl group into the corresponding carbamates 14 and 15. Both compounds, after elaboration of the chain geminal to the nitro group into a vinyl appendage, underwent regio- and stereo-selective removal of the nitro group by palladium-catalyzed displacement with hydride generated by formate to give the precursor 19, easily converted by treatment with hydrochloride acid to 1, isolated as hydrochloride.