The elusive enamine intermediate in proline-catalyzed aldol reactions: NMR detection, formation pathway, and stabilization trends.
Schmid, M. B., Zeitler, K. and Gschwind, R. M.
(2010)
The elusive enamine intermediate in proline-catalyzed aldol reactions: NMR detection, formation pathway, and stabilization trends.
Angew. Chem. Int. Ed. 49 (29), pp. 4997-5003.
Date of publication of this fulltext: 24 Sep 2010 07:54
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| Item type | Article | ||||
| Journal or Publication Title | Angew. Chem. Int. Ed. | ||||
| Publisher: | WILEY-BLACKWELL | ||||
|---|---|---|---|---|---|
| Place of Publication: | MALDEN | ||||
| Volume: | 49 | ||||
| Number of Issue or Book Chapter: | 29 | ||||
| Page Range: | pp. 4997-5003 | ||||
| Date | 2010 | ||||
| Institutions | Chemistry and Pharmacy > Institut für Organische Chemie > Arbeitskreis Prof. Dr. Ruth Gschwind Chemistry and Pharmacy > Institut für Organische Chemie > Alumni or Retired Professors > Arbeitskreis Dr. Kirsten Zeitler | ||||
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| Keywords | ASYMMETRIC ORGANOCATALYSIS; ALDEHYDES; IMIDAZOLIDINONES; 3-HYDROXYFLAVONE; AMINOCATALYSIS; OXAZOLIDINONES; AMINATION; MECHANISM; SOLVENTS; ACIDS; aldol reaction; enamines; NMR spectroscopy; organocatalysis; proline catalysis | ||||
| Dewey Decimal Classification | 500 Science > 540 Chemistry & allied sciences | ||||
| Status | Published | ||||
| Refereed | Yes, this version has been refereed | ||||
| Created at the University of Regensburg | Yes | ||||
| Item ID | 16402 |
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