Jerome Waser

Full Professor

EPFL

Switzerland

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Jerome Waser is a Full Professor at EPFL, Switzerland. His research areas include peptide and protein functionalization, alkyne umpolung strategies, and photoredox catalysis. He has recently contributed to significant advancements in the azidofunctionalization of alkenes and cyclopropenium cation transfer reactions. Additionally, he serves as an Editor-in-Chief for Helvetica Chimica Acta.

Jerome Waser

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Articles (20)

The Azidofunctionalization of Alkenes

Peptide/Protein Functionalization and Macrocyclization via Alkyne Umpolung with Hypervalent Iodine Reagents

Unlocking σ-Type Cyclopropenium Cation Transfer Reactions by an Iodine(III)-Based Umpolung Strategy

Peptide‐Carbazolyl Cyanobenzene Conjugates: Enabling Biomolecule Functionalization via Photoredox and Energy Transfer Catalysis

Peptide‐Carbazolyl Cyanobenzene Conjugates: Enabling Biomolecule Functionalization via Photoredox and Energy Transfer Catalysis

Synthesis of Bicyclo[1.1.1]Pentane Z‐Substituted Enamides, Enol Ethers, and Vinyl Sulfides Using Iodine (III) Reagents

Synthesis of Bicyclo[1.1.1]Pentane Z‐Substituted Enamides, Enol Ethers, and Vinyl Sulfides Using Iodine (III) Reagents

Beginning of Second Mandate as Editors‐in‐Chief for Helvetica Chimica Acta

Photomediated aliphatic C–H functionalization

Photocatalyzed Azidofunctionalization of Alkenes via Radical‐Polar Crossover

Semipinacol Rearrangement of Cyclopropenylcarbinols for the Synthesis of Highly Substituted Cyclopropanes

Photochemical [2+2] Cycloaddition of Alkynyl Boronates

Peptide‐Hypervalent Iodine Reagent Chimeras: Enabling Peptide Functionalization and Macrocyclization**

Peptide‐Hypervalent Iodine Reagent Chimeras: Enabling Peptide Functionalization and Macrocyclization**

Synthese von Trifluormethylierten Alkenen: hypervalentes Iod trifft hochvalentes Kupfer

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

Copper (I)‐BOX Catalyzed Asymmetric 3‐Component Reaction for the Synthesis of Trifluoromethylated Propargylic Ethers and Anilines**

Copper (I)‐BOX Catalyzed Asymmetric 3‐Component Reaction for the Synthesis of Trifluoromethylated Propargylic Ethers and Anilines**

Donor‐Acceptor Aminocyclobutane Monoesters: Synthesis and Silylium‐Catalyzed (4+2) Annulation with Indoles

Donor‐Acceptor Aminocyclobutane Monoesters: Synthesis and Silylium‐Catalyzed (4+2) Annulation with Indoles

Collaborators (1)

Oleksandr O. Grygorenko

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