Alkene Oxyamination Using Malonoyl Peroxides: Preparation of Pyrrolidines and Isoxazolidines
journal contributionposted on 29.05.2018, 19:18 by Carla Alamillo-Ferrer, Jonathan M. Curle, Stuart C. Davidson, Simon C. C. Lucas, Stephen J. Atkinson, Matthew Campbell, Alan R. Kennedy, Nicholas C. O. Tomkinson
Treatment of homoallylic N-tosyl amines or allylic N-tosyl hydroxylamines with 1.5 equiv of a malonoyl peroxide provides a stereoselective method to access functionalized pyrrolidines and isoxazolidines. This metal free alkene oxyamination proceeds in 50–85% yield and up to 13:1 trans-selectivity. In addition, the relative stereochemistry of the oxygen and nitrogen substituents can be inverted through an oxidation/reduction sequence or inverting the stereochemistry of the starting alkene. Mechanistic investigations show a higher reactivity for hydroxyl nucleophiles over sulfonamide nucleophiles revealing a preference for dioxygenation over oxyamination.
Read the peer-reviewed publication
homoallylic NMechanistic investigations showPyrrolidine1.5 equivmalonoyl peroxidestereoselective methodselectivityaccess functionalized pyrrolidinessequencesulfonamide nucleophilesreactivityallylic Ntosyl hydroxylaminesdioxygenationoxidationnitrogen substituentsalkene oxyamination proceedsisoxazolidinePreparationhydroxyl nucleophilesstereochemistrytosyl aminesIsoxazolidines TreatmenttranpreferenceMalonoyl PeroxidesAlkene Oxyaminationinverting