Asymmetric syntheses of benzaldehyde and o-anisaldehyde methyl isopropyl acetals
Asymmetric syntheses of (+)-(αR)-benzaldehyde and (+)-(αR)-o-anisaldehyde methyl isopropyl acetals in 93 and > 95% ee respectively using methodology based on the stereoselective reactions of enantiopure (ortho-substituted benzaldehyde) chromium tricarbonyl complexes are described.
| Autores principales: | , |
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| Formato: | Journal article |
| Lenguaje: | English |
| Publicado: |
1996
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| Sumario: | Asymmetric syntheses of (+)-(αR)-benzaldehyde and (+)-(αR)-o-anisaldehyde methyl isopropyl acetals in 93 and > 95% ee respectively using methodology based on the stereoselective reactions of enantiopure (ortho-substituted benzaldehyde) chromium tricarbonyl complexes are described. |
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