Chemical Communications · 2019 · 13 citations · 26 references
Natural SciencesChemistryMedicinal ChemistryCatalysisOrganic ChemistrySynthetic Medicinal ChemistryHeterocycle SynthesisHeterocyclic ChemistryOrganic SynthesisAmine FunctionalizationEnantioselective SynthesisOrganocatalysisOzonolysisPiperidine ChemistryPiperidine SynthesisStereoselective SynthesisStereospecific Reaction Design
An organocatalytic desymmetrizing intramolecular aza-Michael reaction with vinyl sulfonamides as nucleophilic nitrogen source has been devised for the synthesis of a new family of 2,5,5-trisubstituted piperidines bearing a quaternary sterocenter. The process takes place with excellent levels of enantioselectivity and moderate to good diastereoselectivity. The vinyl sulfonamide moiety can be removed by means of an ozonolysis reaction.
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Maxime G. P. Buffat · Tetrahedron · 2004 · 546 citations
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