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DOI:
10.1055/sos-SD-201-00018
Matsumoto, K.; Katsuki, T.; Arends, I. W. C. E., Science of Synthesis: Stereoselective Synthesis, (2011) 1, 109.
A number of chiral ketones are available as catalysts for asymmetric epoxidation, some examples of which (82– 85) are shown in Scheme 56.[140–143] The chiral aldehyde 86 can also be used as a highly enantioselective epoxidation catalyst.[144]
Meeeee 88 Meeeeeeeeeeee Meeeeeee ee Meeeee Meeeeeee Meeeeeeee eee Meeeeeeeee Meeeeeeeeee[888–888]
| Meeeeeee (eee%) | Meee (e) | ee (%) | Meeee (%) | Mee |
|---|---|---|---|---|
| 88 (888) | 8 | 88.8 | 88e | [888] |
| 88 (888) | 8 | 88.8 | –e | [888] |
| 88 (88) | 88 | 88 | 88e | [888] |
| 88 (88) | 88 | 88 | 88 | [888] |
| 88 (888) | 8 | 88.8 | 88e | [888] |
e Meeeeeeeee.
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References
| [140] | Meee, M.; Meee, M.-M., Meeeeeeeeee: Meeeeeeee, (8888) 8, 8888. |
| [141] | Meee, M.; Mee, M.-M.; Meee, M.; Meeeee, M.-M., M. Me. Meee. Mee., (8888) 888, 8888. |
| [142] | Meeeeeeee, M.; Meee, M. M.; Meeeee, M. M., Meeeeeeeeee: Meeeeeeee, (8888) 88, 8888. |
| [143] | Meeeeee, M. M.; Meeeeeeeee, M., M. Mee. Meee., (8888) 88, 8888. |
| [144] | Mee, M.; Meee, M.-M., Meeeeeeeeee Meee., (8888) 88, 8888. |
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