Abstract
A new class of organocatalysts involving a primary amine as the only functional group is developed for catalytic asymmetric aldol reaction of cyclohexanone/cyclopentanone with various aryl aldehydes in the presence of benzoic acid as an additive at −10∘C. In an unexpected observation, the primary amine catalyzed reactions gave excellent yield and good to excellent stereoselectivity, while secondary amines were found to have little or no reactivity under similar reaction conditions.[Figure not available: see fulltext.]
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Vanlaldinpuia, K., Bora, P., & Bez, G. (2017). Monofunctional primary amine: A new class of organocatalyst for asymmetric Aldol reaction. Journal of Chemical Sciences, 129(3), 301–312. https://doi.org/10.1007/s12039-017-1237-y
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