Publication | Closed Access
The chemistry of small‐ring compounds. Part 40. Protonated and methylated methyleneaziridines
14
Citations
5
References
1978
Year
Chemical Engineering/Sbf 5EngineeringBiochemistryHeterocyclicNatural SciencesSpectra-structure CorrelationOrganic ChemistryChemistryMethyleneaziridines 1A‐cMolecular ChemistryHeterocycle ChemistrySynthetic ChemistryNuclear Magnetic Resonance SpectroscopyHfso 3
Abstract The N ‐substituted methyleneaziridines 1a‐c are protonated on nitrogen without ring rupture by HFSO 3 /SbF 5 in SO 2 at − 78°C. NMR spectra remain unchanged up to + 50°C. Methylation of la does not take place with ordinary methylating agents but can be achieved with (CH 3 ) 2 Cl ⊕ SbF 5 Cl ⊖ .
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