6533b872fe1ef96bd12d306d
RESEARCH PRODUCT
A five-step synthesis of (±)-tylophorine via a nitrile-stabilized ammonium ylide.
Günther LahmTill OpatzAlexander Stoyesubject
chemistry.chemical_classificationNitrileMolecular StructureStereochemistryOrganic ChemistryIndolizinesPhenanthrenesQuaternary Ammonium Compoundschemistry.chemical_compoundAlkaloidschemistryStevens rearrangementYlideNitrilesOrganic chemistryAmmoniumProtecting groupdescription
The Stevens rearrangement of a nitrile-stabilized ammonium ylide is the key step of a very short and practical synthesis of the phenanthroindolizine alkaloid (±)-tylophorine. The method requires only five linear steps and is devoid of any protecting group manipulations.
year | journal | country | edition | language |
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2012-07-19 | The Journal of organic chemistry |