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Angewandte Chemie International Edition, ISSN 1433-7851, 01/2017, Volume 56, Issue 1, pp. 314 - 318
Despite the importance of stapled peptides for drug discovery, only few practical processes to prepare cross‐linked peptides have been described; thus the... 
palladium | peptides | stapled peptides | C−H activation | macrocycles | DIVERSIFICATION | NATURAL-PRODUCTS | ARYLATION | CHEMISTRY, MULTIDISCIPLINARY | FUNCTIONALIZATION | C-H activation | AMINO-ACIDS | RESIDUES | MACROCYCLIZATION | Amino acids | Crosslinked polymers | Palladium | Drug discovery | Peptides | Activation
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 01/2017, Volume 56, Issue 4, pp. 1073 - 1076
A palladium‐catalyzed reaction of primary amines with iodoarenes produces γ‐arylated primary amines. A bulky salicylaldehyde, which is marked as easily... 
amines | reaction mechanisms | palladium | C−H activation | arylation | FUNCTIONALIZATION | PICOLINAMIDE | C-H activation | LIGANDS | COMPLEXES | PRIMARY AMINES | CHEMISTRY, MULTIDISCIPLINARY | Palladium | Buttresses | Amines | Hydrogen bonds
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 08/2018, Volume 57, Issue 33, pp. 10554 - 10558
Journal Article
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 09/2017, Volume 56, Issue 40, pp. 12288 - 12291
Utilizing halogens as traceless directing goups represents an attractive strategy for C−H functionalization. A two C−H alkylation system, initiated by the... 
alkylation | palladium | C−H activation | arenes | cyclization | DOMINO REACTION | INTRAMOLECULAR ARYLATION | BIS-ANNELATED BENZENES | BOND FORMATION | N BOND | CHEMISTRY, MULTIDISCIPLINARY | DIRECTING GROUPS | FUNCTIONALIZATION | C-H activation | ARYL CHLORIDES | PROTON-ABSTRACTION MECHANISM | Palladium | Carbon-carbon composites | Halides | Halogens | Chemical bonds | Biocompatibility | Activation | Alkylation
Journal Article