Improved conditions for the proline-catalyzed aldol reaction of acetone with aliphatic aldehydes

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Abstract

The proline-catalyzed asymmetric aldol reaction between aliphatic aldehydes and acetone has, to date, remained underdeveloped. Challenges in controlling this reaction include avoiding undesired side reactions such as aldol condensation and self-aldolization. In recent years we have developed optimized conditions, which enable high yields and good to excellent enantioselectivities, and which are presented in this communication. © Georg Thieme Verlag Stuttgart New York.

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Martínez, A., Zumbansen, K., Döhring, A., Van Gemmeren, M., & List, B. (2014). Improved conditions for the proline-catalyzed aldol reaction of acetone with aliphatic aldehydes. Synlett, 25(7), 932–934. https://doi.org/10.1055/s-0033-1340919

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