6533b86efe1ef96bd12cc9c6
RESEARCH PRODUCT
A novel and selective fluoride opening of aziridines by XtalFluor-E. synthesis of fluorinated diamino acid derivatives.
Loránd KissSantos FusteroFerenc FülöpMatti HaukkaMelinda Nonnsubject
chemistry.chemical_classificationTetrafluoroborateBicyclic moleculesynthesisOrganic ChemistryRegioselectivitycarboxylatesAziridineBiochemistryMedicinal chemistrySulfonamidechemistry.chemical_compoundchemistryaziridinesfluorineLactamMoietyOrganic chemistryPhysical and Theoretical ChemistryFluorideta116description
The selective introduction of fluorine onto the skeleton of an aminocyclopentane or cyclohexane carboxylate has been developed through a novel and efficient fluoride opening of an activated aziridine ring with XtalFluor-E. The reaction proceeded through a stereoselective aziridination of the olefinic bond of a bicyclic lactam and regioselective aziridine ring opening with difluorosulfiliminium tetrafluoroborate with the neighboring group assistance of the sulfonamide moiety to yield fluorinated diamino acid derivatives. The method based on the selective aziridine opening by fluoride has been generalized to afford access to mono- or bicyclic fluorinated substances.
| year | journal | country | edition | language |
|---|---|---|---|---|
| 2015-01-01 | Organic letters |