Intermolecular tandem-Michael/Michael addition reactions of alkyne acceptors and CH-acidic compounds such as 1,3-cyclohexanedione (2a) and dimedone (2b) under L-proline catalysis furnished four new products 1a-d with C 2 axial chirality. © Wiley-VCH Verlag GmbH & Co. KGaA, 2008.
CITATION STYLE
Luna, L. E., Seoane, G., & Cravero, R. M. (2008). Synthesis and characterization of atropisomers arising from 1,3-cyclohexanediones by intermolecular tandem-Michael/Michael additions. European Journal of Organic Chemistry, (7), 1271–1277. https://doi.org/10.1002/ejoc.200700803
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