Full Text Available
Note: Clicking the button above will open the full text document at the original institutional repository in a new window.
Hemiaminals : a new chemotype for organocatalysis
Jorgensen and List introduced enantioselective α-amination of an aldehyde with an azodicarboxylate as the electrophile using L -proline enamine catalysis in 2002. Following borohydride reduction, the α-hydrazino alcohol was obtained in high yield (93-99%) and enantioselectivity (86-97%). Application...
Saved in:
| Main Author: | |
|---|---|
| Other Authors: | |
| Format: | Thesis |
| Language: | English |
| Published: |
Department of Chemistry
2015
|
| Subjects: | |
| Tags: |
No Tags, Be the first to tag this record!
|
Similar Items: Hemiaminals : a new chemotype for organocatalysis
- Synthesis of 1,4 Dihydropyridines as potential antimalarial chemotype
- Sceletium tortuosum (L.) N.E. Br.: mesembrine alkaloid chemotype signatures in wild type, cultivated and in vitro tissues
- The structure and reactivity of N-Acyl phosphoric amides and related systems
- ASH: a new protein domain on the horizon
- ASH: a new protein domain on the horizon
- New CO₂ chemistry for fine chemical synthesis