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DOI: 10.1055/s-0028-1087719
Structure of Reactive Intermediates of Organocatalysis
D. Seebach*, U. Groelj, D. M. Badine, W. B. Schweizer, A. K. Beck
ETH Zürich, Switzerland
Publikationsverlauf
Publikationsdatum:
19. Februar 2009 (online)

Significance
The present work of the Seebach group addresses the isolation and characterization of reactive intermediates in organocatalysis. In this regard, enamine 1 and iminium tetrafluoroborates 2-4 were prepared through conventional methods from 2-phenyl acetaldehyde or cinnamaldehyde, respectively, and the corresponding secondary amine (salt) catalyst. Single crystals of enamine 1 and iminium ions 2 and 3 were subjected to Röntgen structure analysis. The structure of iminium ion 4 was elucidated by 2D NMR spectroscopy. Moreover, the Röntgen and NMR structures were extensively discussed in connection with other, structurally related compounds.