| Bioactivity | H-Pro-Pro-Asp-NH2 is a potent and selective catalyst for asymmetric aldol reactions. H-Pro-Pro-Asp-NH2 catalyzes aldol reactions between acetone and several aldehydes[1][2]. |
| Name | H-Pro-Pro-Asp-NH2 |
| CAS | 850440-85-6 |
| Sequence | H-Pro-Pro-Asp-NH2 |
| Shortening | PPD |
| Formula | C14H22N4O5 |
| Molar Mass | 326.35 |
| Transport | Room temperature in continental US; may vary elsewhere. |
| Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
| Reference | [1]. Revell JD, et al. Solid-supported and pegylated H-Pro-Pro-Asp-NHR as catalysts for asymmetric aldol reactions. Biopolymers. 2006;84(1):105-13. [2]. Jefferson D. Revell, et al. Investigating Sequence Space: How Important is the Spatial Arrangement of Functional Groups in the Asymmetric Aldol Reaction Catalyst H-Pro-Pro-Asp-NH2? Advanced Synthesis & Catalysis, 2008, 1046-1052. |