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- W2517646245 abstract "Screenings of peptide libraries with N‐terminal l ‐ or d ‐proline were performed under aqueous conditions to obtain capable catalysts for the asymmetric Michael addition of a malonate. From a d ‐prolyl peptide library, a consensus sequence, d ‐Pro‐ d ‐Pro‐X‐Trp‐X 3 , was found, and the peptide possessing lysine in this framework showed good reactivity and enantioselectivity. The presence of the tryptophan residue at the fourth position was essential and replacing it with a pyrenylalanine residue further improved the catalytic ability. With an optimum peptide, the reaction could be promoted efficiently in aqueous media at a low catalyst loading." @default.
- W2517646245 created "2016-09-16" @default.
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- W2517646245 date "2016-08-30" @default.
- W2517646245 modified "2023-10-01" @default.
- W2517646245 title "Library Screening in Aqueous Media To Develop a Highly Active Peptide Catalyst for Enantioselective Michael Addition of a Malonate" @default.
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- W2517646245 doi "https://doi.org/10.1002/ejoc.201600828" @default.
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