Publication | Open Access
Asymmetric Synthesis of All Stereoisomers of Isofagomine Using [2,3]-Wittig Rearrangement
23
Citations
38
References
2007
Year
Asymmetric CatalysisEngineeringAsymmetric SynthesisOrganic ChemistryO-alkylstannylmethyl Compound 5Stereoselective SynthesisChemistryNatural Product Synthesis5-Hydroxymethyl-3-piperidene 6Synthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
The asymmetric synthesis of all stereoisomers of isofagomine from 5-hydroxymethyl-3-piperidene 6, which was prepared by [2,3]-Wittig rearrangement of O-alkylstannylmethyl compound 5 derived from readily available chiral 3-hydroxypiperidene 4, is described.
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