The direct route: Iridium-catalyzed direct conversion of branched allylic alcohols into enantioenriched branched primary allylic amines is highly regio- and enantioselective (see scheme; coe=cyclooctene). Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
CITATION STYLE
Lafrance, M., Roggen, M., & Carreira, E. M. (2012). Direct, enantioselective iridium-catalyzed allylic amination of racemic allylic alcohols. Angewandte Chemie - International Edition, 51(14), 3470–3473. https://doi.org/10.1002/anie.201108287
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