Diarylprolinol in an asymmetric aldol reaction of an -alkyl--oxo aldehyde as an electrophileThis article is part of the joint ChemCommOrganic & Biomolecular Chemistry Organocatalysis web themed issue.Electronic supplementary information (ESI) available. See DOI: 10.1039/c2cc31230a
The direct aldol reaction of an -alkyl--oxo aldehyde was catalyzed by trifluoromethyl-substituted diarylprolinol 1 to afford a -oxo--hydroxy--substituted aldehyde in good yield with excellent anti -selectivity and excellent enantioselectivity. The direct aldol reaction of an -alkyl--oxo aldehyde was...
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Sprache: | eng |
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Zusammenfassung: | The direct aldol reaction of an -alkyl--oxo aldehyde was catalyzed by trifluoromethyl-substituted diarylprolinol
1
to afford a -oxo--hydroxy--substituted aldehyde in good yield with excellent
anti
-selectivity and excellent enantioselectivity.
The direct aldol reaction of an -alkyl--oxo aldehyde was catalyzed by trifluoromethyl-substituted diarylprolinol to afford a -oxo--hydroxy--substituted aldehyde in good yield with excellent
anti
-selectivity and excellent enantioselectivity. |
---|---|
ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/c2cc31230a |