Table 2. Enantioselective α-Trifluoromethylation: Aldehyde Scope.
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---|---|---|---|---|---|
entry | producta | yield,b eec | entry | producta | yield,b eec |
1 |
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79% yield 99% ee | 7 |
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73% yieldd 90% ee |
2 |
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72% yield 95% ee | 8 |
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61% yield 93% ee |
3 |
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86% yield 97% ee | 9 |
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75% yield 97% ee |
4 |
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78% yield 98% ee | 10 |
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68% yield >20:1 dr 99% ee |
5 |
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X = CH2 70% yield 99% ee | 11 |
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62% yield >20:1 dr 99% ee |
6 | X = NBoc 70% yield 98% ee |
Stereochemistry assigned by chemical correlation or by analogy.
Isolated yields of the corresponding alcohol.
Enantiomeric excess determined by chiral SFC or HPLC analysis.
Using catalyst 11; ref 20.