Tetrahedron p. 2583 - 2590 (1994)
Update date:2022-08-03
Topics:
Barco, Achille
Benetti, Simonetta
De Risi, Carmela
Pollini, Gian P.
Romagnoli, Romeo
Spalluto, Giampiero
Zanirato, Vinicio
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.
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Doi:10.1246/cl.1994.63
(1994)Doi:10.1021/jo00088a053
(1994)Doi:10.1039/c3cc49116a
(2014)Doi:10.1016/S0960-894X(97)00199-6
(1997)Doi:10.1002/ejoc.201201075
(2012)Doi:10.1021/jm00037a020
(1994)