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The pH of the reaction controls the stereoselectivity of organocatalyzed direct aldol reactions in water
Authors:Swapandeep Singh Chimni  Sarbjit Singh  Akshay Kumar
Institution:aDepartment of Chemistry, Guru Nanak Dev University, Amritsar 143 005, India
Abstract:The direct aldol reaction of 4-nitrobenzaldehyde and cyclohexanone, catalyzed by a protonated prolinamide catalyst in water, proceeds with the formation of aldol product that has high diastereoselectivity and enantioselectivity in an optimal pH range of 4–5.
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