Organic & Biomolecular Chemistry · 2010 · 38 citations · 70 references
Natural SciencesChemistryMedicinal ChemistryCatalysisOrganic ChemistrySynthetic Medicinal ChemistryHeterocycle SynthesisHeterocyclic ChemistryOrganic SynthesisAsymmetric Heterocycle SynthesisEnantioselective SynthesisPiperidine AlkaloidsPiperidine ChemistryPiperidine SynthesisQuinone MethidesTotal Synthesis-derived Analogues
A general and efficient procedure for the preparation of 2,6-disubstituted piperidines bearing one alkene- or alkyne-containing substituent was developed by using non-racemic Betti base as a chiral auxiliary. Many chiral benzylamines are excellent auxiliaries, but they were rarely used for this purpose because of the inefficient removal of the N-benzyl auxiliary residue under non-hydrogenative conditions. We found that N,N-disubstituted Betti base derivative has a typical Mannich structure of o-naphthol. When it carried out a base-catalyzed formation of o-quinone methide, an efficient non-hydrogenative N-debenzylation was achieved, and the alkene and alkyne groups survived. To demonstrate the efficiency of the method and the versatility of the products, asymmetric total syntheses of indolizidine-alkaloids (-)-167B, (-)-195H, (-)-209D and (-)-223AB were accomplished.
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Stereoselective Synthesis of Piperidines
Sabine Laschat, Tim Dickner · Synthesis · 2000 · 377 citations
Asymmetric routes to substituted piperidines
Patrick D. Bailey, Paula A. Millwood, Peter D. Smith · Chemical Communications · 1998 · 328 citations
Indolizidine and quinolizidine alkaloids
Joseph P. Michael · Natural Product Reports · 2007 · 261 citations