Table 3.
Diastereoselective reaction by using chiral oxazolyl ferrocene 1b.
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| entry | R | time (h) | product | yield (%) |
| 1 | Ph | 2 | 3a | 43 |
| 2 | 4-MeOC6H4 | 2 | 3b | 24 |
| 3 | 4-ClC6H4 | 2 | 3c | 38 |
| 4 | benzyl | 2 | 3d | 32 |
| 5 | n-butyl | 24 | 3e | 69 |
| 6 | cyclohexyl | 24 | 3f | 38 |
Diastereoselective reaction by using chiral oxazolyl ferrocene 1b.
![]() | ||||
| entry | R | time (h) | product | yield (%) |
| 1 | Ph | 2 | 3a | 43 |
| 2 | 4-MeOC6H4 | 2 | 3b | 24 |
| 3 | 4-ClC6H4 | 2 | 3c | 38 |
| 4 | benzyl | 2 | 3d | 32 |
| 5 | n-butyl | 24 | 3e | 69 |
| 6 | cyclohexyl | 24 | 3f | 38 |