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Results for ALPHA-LITHIATION-REARRANGEMENT

Publications & Outputs

  1. Unexpected products from the attempted organolithium-mediated conversion of beta-methoxy aziridines into allylic amines

    Coote, S. C. & O'Brien, P., 27/01/2010, In: Tetrahedron Letters. 51, 4, p. 588-590 3 p.

    Research output: Contribution to Journal/MagazineJournal articlepeer-review

  2. Stereoselective aziridination of cyclic allylic alcohols using chloramine-T

    Coote, S. C., O'Brien, P. & Whitwood, A. C., 2008, In: Organic and Biomolecular Chemistry . 6, 23, p. 4299-4314 16 p.

    Research output: Contribution to Journal/MagazineJournal articlepeer-review

  3. New route to azaspirocycles via the organolithium-mediated conversion of beta-alkoxy aziridines into cyclopentenyl amines

    Moore, S. P., Coote, S. C., O'Brien, P. & Gilday, J., 26/10/2006, In: Organic Letters. 8, 22, p. 5145-5148 4 p.

    Research output: Contribution to Journal/MagazineJournal articlepeer-review

  4. Reductive alkylation of beta-alkoxy aziridines: new route to substituted allylic amines

    Rosser, C. M., Coote, S. C., Kirby, J. P., O'Brien, P. & Caine, D., 23/12/2004, In: Organic Letters. 6, 26, p. 4817-4819 3 p.

    Research output: Contribution to Journal/MagazineJournal articlepeer-review