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Jerome Waser

Full Professor

EPFL

Switzerland

Research Interests

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Professors in Switzerland Professors in Organic Chemistry Organic Chemistry professors in Switzerland

About

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.

Articles (33)

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Collaborators (10)

Alexandre Schoepfer

University of Utah

UNITED STATES

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Javier Pérez-Ramírez

Professor

ETH Zurich

SWITZERLAND

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Stefano Nicolai

Scientist

EPFL (École Polytechnique Fédérale de Lausanne)

SWITZERLAND

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Sharon Mitchell

Permanent lecturer

Swiss Federal Institute of Technology in Zurich

SWITZERLAND

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Oleksandr O. Grygorenko

Head of Organic Chemistry Department

UKRAINE

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Luca Chiapperino

Full Professor UAS

University of Lausanne

SWITZERLAND

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Eva Hevia

Professor

University of Bern

SWITZERLAND

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Matthew Wodrich

Research Scientist

EPFL (École Polytechnique Fédérale de Lausanne)

SWITZERLAND

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Francesco Panese

Full Professor

University of Lausanne

SWITZERLAND

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Géraldine Masson

Deputy Director of ICSN

Université Paris-Saclay

FRANCE

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Jerome Waser

Research Interests

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About

Articles (33)

6 Synthesis and Applications of Alkynylbenziodoxol(on)es

Navigating sustainability transitions in the chemical sciences: insights from an instant qualitative survey

Feature Selection in Multivariate Linear Regression Models for Data-Efficient Reaction Optimization

Alcohol‐Directed Carboamination of Conjugated Enynes

From Complex Targets to General Methods: Celebrating Jieping Zhu's 60th Birthday

Diastereoselective Synthesis of Housanes via the Carbocupration of Cyclopropenes

Formal Synthesis of the Akuammiline Alkaloid (±)‐Strictamine via a (4 + 2) Annulation Reaction With a Donor–Acceptor Cyclobutane

Accessing CF3-Cyclopropenes ─ A Platform for the Synthesis of Trifluoromethylated Building Blocks

Synthesis of Csp3 Chlorinated Compounds from Cyclopropanes, Olefins, and C–H Bonds via Photolysis of Willgerodt-Type Reagents

1 Introduction

Stereoselective palladium-catalyzed carboetherification of cyclopropenes via a tethering strategy

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

Ligand-Directed Site-Selective Cysteine Bioconjugation of the KELCH Domain of KEAP1 with Hypervalent Iodine Reagents

Cycloaddition and Annulation Reactions with Donor‐Acceptor Cyclobutanes

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 (10)

Alexandre Schoepfer

Javier Pérez-Ramírez

Stefano Nicolai

Sharon Mitchell

Oleksandr O. Grygorenko

Luca Chiapperino

Eva Hevia

Matthew Wodrich

Francesco Panese

Géraldine Masson

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