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Inside Back Cover: Suzuki–Miyaura Diversification of Amino Acids and Dipeptides in Aqueous Media (ChemCatChem 14/2015)
Author(s) -
Willemse Tom,
Van Imp Karolien,
Goss Rebecca J. M.,
Van Vlijmen Herman W. T.,
Schepens Wim,
Maes Bert U. W.,
Ballet Steven
Publication year - 2015
Publication title -
chemcatchem
Language(s) - English
Resource type - Reports
SCImago Journal Rank - 1.497
H-Index - 106
eISSN - 1867-3899
pISSN - 1867-3880
DOI - 10.1002/cctc.201500742
Subject(s) - dipeptide , aqueous medium , chemistry , palladium , peptide , combinatorial chemistry , phenylalanine , catalysis , amino acid , aqueous solution , cover (algebra) , organic chemistry , biochemistry , engineering , mechanical engineering
The Inside Back Cover picture shows palladium‐catalyzed derivatisations of halogenated phenylalanine and tryptophan and dipeptide substrates containing these entities in view of the optimization of lead peptide ligands for improved receptor interactions. A wide scope of substrates is presented to highlight the tolerated peptide functionality during the application of the Suzuki‐Miyaura reaction in aqueous media. In their Full Paper, T. Willemse et al. investigate the influence of unprotected peptide functionalities on the progress of the Pd‐catalyzed reaction. In the background, the collaboration between the Maes and Ballet laboratories is emphasized by the skylines of Antwerp and Brussels. The article highlighted by this cover can be found on p. 2055 ff. of Issue 14, 2015.