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Angewandte Chemie International Edition, ISSN 1433-7851, 01/2018, Volume 57, Issue 1, pp. 203 - 207
Secondary C(sp 3 )−H arylations were accomplished by palladium catalysis with triazoles as peptide bond isosteres. The unique power of this approach is... 
triazoles | palladium | peptides | amino acids | arylation | DIRECTING GROUP | ALPHA-AMINO-ACIDS | UNACTIVATED C(SP)-H | CARBON-HYDROGEN BONDS | DIRECT ARYLATIONS | C-H ACTIVATION | CHEMISTRY, MULTIDISCIPLINARY | FUNCTIONALIZATION | PEPTIDOMIMETICS | COUPLING REACTIONS | Amino acids | Palladium | Catalysis | Peptides | Triazoles
Journal Article
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 | CATALYSIS | COMPLEXES | C-H FUNCTIONALIZATION | CHEMISTRY, MULTIDISCIPLINARY | PICOLINAMIDE | C-H activation | LIGANDS | COUPLING REACTIONS | ALIPHATIC-AMINES | Palladium | Buttresses | Amines | Hydrogen bonds
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 08/2018, Volume 57, Issue 33, pp. 10554 - 10558
Late‐stage BODIPY diversification of structurally complex amino acids and peptides was accomplished by racemization‐free palladium‐catalyzed C(sp 3 )−H... 
triazoles | H activation | peptides | BODIPY | C(sp | labeling | TRYPTOPHAN | PALLADIUM | DYES | DIVERSIFICATION | ALPHA-AMINO-ACIDS | CARBON-HYDROGEN BONDS | C-H ACTIVATION | CHEMISTRY, MULTIDISCIPLINARY | CATALYZED ARYLATION | ALKYL-HALIDES | FUNCTIONALIZATION | C(sp)-H activation | Chemotherapy | Peptides | Triazoles | Fluorescence | Amino acids | Palladium | Labeling | Cancer | Racemization | Activation
Journal Article
Angewandte Chemie - International Edition, ISSN 1433-7851, 02/2013, Volume 52, Issue 9, pp. 2593 - 2598
The other side of the mountain: Changing the framework of diyne systems opens up new cyclization modes for dual gold catalysis. Instead of a 5-endo cyclization... 
gold | C-H activation | dual catalysis | computational chemistry | alkynes | C-H BOND | ORGANIC-REACTIONS | COMPLEXES | PLATINUM | TERMINAL ALKYNES | CASCADE | AROMATIZATION | CHEMISTRY, MULTIDISCIPLINARY | FUNCTIONALIZATION | CH activation | CYCLOISOMERIZATION | DERIVATIVES | Antirheumatic agents | Catalysis | Mountains | Gold | Pathways | Switches | Insertion | Activation | Carbenes
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
Advanced Synthesis & Catalysis, ISSN 1615-4150, 05/2014, Volume 356, Issue 7, pp. 1461 - 1479
Journal Article