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Proline-Catalysed Amination Reactions in Cyclic Carbonate Solvents
School of Chemistry, Research Centre in Catalysis and Intensified Processing, Bedson Building, University of Newcastle, Newcastle upon Tyne, NE1 7RU, UK
* Author to whom correspondence should be addressed.
Received: 6 April 2011; in revised form: 19 April 2011 / Accepted: 20 April 2011 / Published: 21 April 2011
Abstract: Propylene carbonate is shown to be an environmentally friendly and sustainable replacement for dichloromethane and acetonitrile in proline-catalysed a-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.
Keywords: proline; amination; cyclic-carbonate
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MDPI and ACS Style
Beattie, C.; North, M.; Villuendas, P. Proline-Catalysed Amination Reactions in Cyclic Carbonate Solvents. Molecules 2011, 16, 3420-3432.
Beattie C, North M, Villuendas P. Proline-Catalysed Amination Reactions in Cyclic Carbonate Solvents. Molecules. 2011; 16(4):3420-3432.
Beattie, Christopher; North, Michael; Villuendas, Pedro. 2011. "Proline-Catalysed Amination Reactions in Cyclic Carbonate Solvents." Molecules 16, no. 4: 3420-3432.