N-[(1R)-1-(Hydroxydiphenylmethyl)-3-methylbutyl]-D-prolinamide
Modify Date: 2024-09-17 12:37:06
![N-[(1R)-1-(Hydroxydiphenylmethyl)-3-methylbutyl]-D-prolinamide Structure](https://image.chemsrc.com/caspic/494/1088110-92-2.png)
N-[(1R)-1-(Hydroxydiphenylmethyl)-3-methylbutyl]-D-prolinamide structure
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Common Name | N-[(1R)-1-(Hydroxydiphenylmethyl)-3-methylbutyl]-D-prolinamide | ||
|---|---|---|---|---|
| CAS Number | 1088110-92-2 | Molecular Weight | 366.5 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C23H30N2O2 | Melting Point | 194°C±3°C | |
| MSDS | Chinese USA | Flash Point | N/A | |
| Symbol |
GHS07 |
Signal Word | Warning | |
| Name | N-[(1R)-1-(Hydroxydiphenylmethyl)-3-methylbutyl]-D-prolinamide |
|---|
| Melting Point | 194°C±3°C |
|---|---|
| Molecular Formula | C23H30N2O2 |
| Molecular Weight | 366.5 |
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Highly enantioselective direct aldol reaction catalyzed by organic molecules.
Org. Lett. 8 , 4097-4099, (2006) We have demonstrated that a new class of l-proline-based organic compounds catalyzed the direct aldol reaction between aldehydes and acetone to provide beta-hydroxy ketones in good yields. The reactio... |
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Direction of Kinetically versus Thermodynamically Controlled Organocatalysis and Its Application in Chemoenzymatic Synthesis Rulli, G., et al.
Angew. Chem. Int. Ed. Engl. 50 , 1-5, (2011)
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