Rhodium-catalyzed asymmetric intramolecular hydroamination of unactivated alkenes

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Abstract

(Figure Presented) One for the Rh(oad): The first rhodiumcatalyzed asymmetric intramolecular hydroamination of unactivated olefins was developed by using dialkylbiaryl phosphine ligands (see scheme; cod = 1,5-cyclooctadiene, Cy = cyclohexyl). A variety of 2-methylpyrrolidines have been synthesized with high enantioselectivities. © 2010 Wiley-VCH Verlag GmbH & Co. KGaA.

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Shen, X., & Buchwald, S. L. (2010). Rhodium-catalyzed asymmetric intramolecular hydroamination of unactivated alkenes. Angewandte Chemie - International Edition, 49(3), 564–567. https://doi.org/10.1002/anie.200905402

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