Using the reaction between phenylacetaldehyde and nitrostyrene catalyzed by pyrrolidine as a simple model, we have studied the diastereochemical outcome of the organocatalytic Michael reactions between benzylic aldehydes and nitrostyrenes. We found that the anti adduct was obtained in high yield and diastereoselection as was demonstrated by the X-ray structure of the product. In situ NMR studies showed a different reaction pathway when compared to aliphatic aldehydes that yield the syn adduct as major isomer.
Donadío, L.G., Galetti, M.A., Giorgi, G., Rasparini, M., Comin, M.J. (2016). Anti-Selective Organocatalytic Michael Addition between Phenylacetaldehyde and Nitrostyrene. JOURNAL OF ORGANIC CHEMISTRY, 81(17), 7952-7957 [10.1021/acs.joc.6b01061].
Anti-Selective Organocatalytic Michael Addition between Phenylacetaldehyde and Nitrostyrene
GIORGI, GIANLUCA;
2016-01-01
Abstract
Using the reaction between phenylacetaldehyde and nitrostyrene catalyzed by pyrrolidine as a simple model, we have studied the diastereochemical outcome of the organocatalytic Michael reactions between benzylic aldehydes and nitrostyrenes. We found that the anti adduct was obtained in high yield and diastereoselection as was demonstrated by the X-ray structure of the product. In situ NMR studies showed a different reaction pathway when compared to aliphatic aldehydes that yield the syn adduct as major isomer.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
https://hdl.handle.net/11365/1001758
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