Proline-catalysed amination reactions in cyclic carbonate solvents

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Abstract

Propylene carbonate is shown to be an environmentally friendly and sustainable replacement for dichloromethane and acetonitrile in proline-catalysed α-hydrazinations of aldehydes and ketones. Enantioselectivities comparable to those obtained in conventional solvents or ionic liquids can be obtained, even when using a lower catalyst loading. © 2011 by the authors.

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Beattie, C., North, M., & Villuendas, P. (2011). Proline-catalysed amination reactions in cyclic carbonate solvents. Molecules, 16(4), 3420–3432. https://doi.org/10.3390/molecules16043420

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