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Sterisch gehinderte Pyrrolidine. Umsetzung von 2,5,5‐Trimethyl‐1‐pyrrolin‐1‐oxid mit α‐Chloracrylnitril
19
Citations
3
References
1982
Year
Diversity Oriented SynthesisBioorganic ChemistryDerivativesAbstract ReactionHeterocyclicNatural SciencesCompound 2ASterisch Gehinderte PyrrolidineOrganic ChemistryNitrone 1ChemistryHeterocycle ChemistryPharmacologyPharmaceutical ChemistrySynthetic Chemistry
Abstract Reaction of the nitrone 1 with α‐chloroacrylonitrile ( 4 ) as ketene equivalent yields the 5‐isoxazolidinone 2a and the α‐chloroimine 5 . The mechanism of the reaction is discussed. The compound 2a is useful for the synthesis of hindered pyrrolidines 3 .
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