Diversity-oriented enantioselective synthesis of highly functionalized cyclic and bicyclic alcohols

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Abstract

The copper-catalyzed hetero-allylic asymmetric alkylation (h-AAA) of functionalized Grignard reagents that contain alkene or alkyne moieties has been achieved with excellent regio- and enantioselectivity. The corresponding alkylation products were further transformed into a variety of highly functionalized cyclic and bicyclic alcohols with excellent control over the chemo-, regio-, and stereoselectivity. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Mao, B., Fañanás-Mastral, M., Lutz, M., & Feringa, B. L. (2013). Diversity-oriented enantioselective synthesis of highly functionalized cyclic and bicyclic alcohols. Chemistry - A European Journal, 19(2), 761–770. https://doi.org/10.1002/chem.201202859

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