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Synfacts 2006(4): 0388-0388
DOI: 10.1055/s-2006-932105
DOI: 10.1055/s-2006-932105
Bioorganic Chemistry and Organocatalysis
© Georg Thieme Verlag Stuttgart · New York
Microwave-Assisted Proline-Catalyzed Direct Asymmetric Mannich Reaction
B. Rodriguez, C. Bolm*
RWTH Aachen, Germany
Further Information
Publication History
Publication Date:
24 March 2006 (online)

Significance
The authors describe a screening of conditions leading to an optimized microwave-assisted protocol for the direct asymmetric (S)-proline-catalyzed Mannich reaction employing cyclohexanone (1), formaldehyde (2) and substituted anilines 3 as substrates. Catalyst loadings of less than 1% have been realized under optimized conditions. The reaction time could be decreased from 30 hours to a maximum of 4 hours, still yielding 44-96% of amines 4 after a reduction step, and the enantioselectivity (94-98% ee) is not diminished under these conditions.