Publication | Closed Access
Stereoselective approaches to 2,3,6-trisubstituted piperidines. An enantiospecific synthesis of quinolizidine (−)-217A
34
Citations
31
References
2011
Year
BiosynthesisEngineeringNatural Product SynthesisStereoselective Approaches2,3,6-Trisubstituted PiperidinesTotal SynthesisOrganic ChemistryEnantiospecific SynthesisStereoselective SynthesisChemistryHeterocycle ChemistryPharmacologyAsymmetric CatalysisEnantioselective SynthesisBiomolecular EngineeringKey Steps
The enantiospecific and diastereocontrolled total synthesis of alkaloid (-)-217A is described that employs a stepwise [3+3] annelation strategy and a piperidine 2,3-cyclopropanation-ring opening reaction as the key steps.
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