Peptides as Asymmetric Catalysts for Aldol Reactions
DOI:
https://doi.org/10.2533/chimia.2007.276Keywords:
Aldol reaction, Asymmetric catalysis, Combinatorial chemistry, PeptidesAbstract
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.Downloads
Published
2007-05-30
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Scientific Articles
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Copyright (c) 2007 Swiss Chemical Society
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
How to Cite
[1]
H. Wennemers, Chimia 2007, 61, 276, DOI: 10.2533/chimia.2007.276.