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Solid-phase peptide synthesis in 384-well plates

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Solid-phase peptide synthesis in 384-well plates

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Methods for high-throughput synthesis and screening of peptide libraries

Improved microfluidic transcriptome based screening methods

Development of methods for the synthesis of large combinatorial libraries of macrocyclic compounds

Peptide-Hypervalent Iodine Reagent Chimeras: Enabling Peptide Functionalization and Macrocyclization

Synthesis of Trifluoromethylated Alkenes: Hypervalent Iodine Meets High-Valent Copper

Development of cyclic peptides that can be administered orally to inhibit disease targets

Generating macrocyclic inhibitors of protein-protein interactions

De novo developed small cyclic peptides that are orally available

Solid-phase peptide synthesis on disulfide-linker resin followed by reductive release affords pure thiol-functionalized peptides

Go to the Board: A Journey through the Life of Professor David A. Evans