Related Experiment Video
Updated: Feb 3, 2026

Protocol for the Synthesis of Ortho-trifluoromethoxylated Aniline Derivatives
Published on: January 19, 2016
Synthesis of Diverse α-Fluoroalkoxyaryl Derivatives and Their Use for the Generation of Fluorinated Macrocycles
Thomas J Cogswell1, Anders Dahlén1, Laurent Knerr1
1Cardiovascular and Metabolic Disease, Innovative Medicines and Early Development, AstraZeneca R&D, Mölndal, SE-431 89, Sweden.
Abstract:
Introduction of difluorinated functionality has emerged as a powerful means for conformational design with minimal steric footprint. Synthetic approaches for the preparation of aryl difluoromethylene ether containing novel building blocks were established, enabling the inclusion of the aryl difluoromethylene ether system into macrocyclic scaffolds for the first time.
Related Concept Videos
α-Halogenation of Carboxylic Acid Derivatives: Overview
Synthesis of α-Substituted Carbonyl Compounds: The Stork Enamine Reaction
Diversity of Archaea I
Cell Diversity
Multicellular...
Diversity of Archaea II
Diversity of Protists I

