Abstract
The article summarizes our research devoted to the development of peptidic catalysts for aldol reactions. Using the combinatorial method of 'catalyst-substrate coimmobilization' the peptides H-Pro-Pro-Asp-NH2 and H-Pro-D-Ala-D-Asp-NH2 were identified as highly active and selective catalysts for direct aldol reactions. The results demonstrate that the higher complexity of peptides in comparison to rigid small organocatalysts can be a good trade-off for higher activity. © Schweizerische Chemische Gesellschaft.
Author supplied keywords
Cite
CITATION STYLE
Wennemers, H. (2007). Peptides as asymmetric catalysts for aldol reactions. Chimia, 61(5), 276–278. https://doi.org/10.2533/chimia.2007.276
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.