Abstract
(Chemical Equation Presented) A new catalytic activity of iron salts for intramolecular hydroamination is revealed. A number of aminoolefins underwent the reaction under mild conditions to form the corresponding pyrrolidine derivatives in good yield. The reaction displayed good functional-group compatibility and resistance to air and moisture. (Ts = e-toluenesulfonyl). © 2006 Wiley-VCH Verlag GmbH & Co. KGaA.
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Komeyama, K., Morimoto, T., & Takaki, K. (2006). A simple and efficient iron-catalyzed intramolecular hydroamination of unactivated olefins. Angewandte Chemie - International Edition, 45(18), 2938–2941. https://doi.org/10.1002/anie.200503789
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