Palladium(II) pincer complexes of α-amino acids: towards the synthesis of catalytically active artificial peptides
✍ Scribed by Gabriela Guillena; Gema Rodrı́guez; Gerard van Koten
- Book ID
- 104251074
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- French
- Weight
- 72 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
NCN palladium(II) complexes have been covalently attached to the N-and C-termini of L-valine and to the N-terminus of the dipeptide L-Phe-L-Val-OMe. Remarkably, the hydrolysis of the NCN-Pd(II) L-Val-OMe compound afforded the corresponding palladated, free amino acid without affecting the metal site. This deprotected amino acid could be coupled to any protein, enzyme or peptidic chain by simple peptide chemistry. These bioorganometallic systems were active as catalysts in the aldol reaction between methyl isocyanate and benzaldehyde.
📜 SIMILAR VOLUMES
## Abstract The synthesis and catalytic applications of a new aryl‐based unsymmetrical PCS‐pincer complex are reported. Preparation of the robust air‐ and moisture‐stable PCS‐pincer palladium complex 5[X] started from the symmetrical α,α′‐dibromo‐__meta__‐xylene and involved the selective substitut