Description
This detailed book highlights several emerging areas in the implementation of green chemistry in medicinal chemistry drug discovery with a specific focus on their application to the expeditious discovery of new biologically active entities. Divided into three sections, the collection explores greener approaches to chemical transformations that are both prevalent and have been highlighted as challenging within the pharmaceutical industry, overall synthetic strategy, as well as the implementation and impact of a range of enabling technologies within medicinal chemistry. As a volume of the Methods in Pharmacology and Toxicology series, chapters provide the kind of key insight that can guide researchers toward greater success in the lab.
Table of Contents
Green Synthesis of Common Heterocycles.- Greener Methods for Amide Bond Synthesis.- Mitsunobu Reactions in Medicinal Chemistry and Development of Practical Modifications.- Direct Nucleophilic Substitution of Alcohols by Brønsted or Lewis Acids Activation: An Update.- Friedel-Crafts Reactions.- Ionic Liquids: Design and Applications.- Designing Efficient Cascade Reactions in Drug Discovery.- Multicomponent Synthesis: Cohesive Integration of Green Chemistry Principles.- Direct C–H Functionalization Approaches to Pharmaceutically Relevant Molecules.- C–H Activation with Photoredox Catalysis.- In Situ Protecting Groups for Chemoselective Transformations.- Expanding the Biocatalysis Toolbox.- New Directions in Coupling Chemistry.- Flow Chemistry as an Enabling Technology for Synthetic Organic Chemistry.- Reaction Optimization: A High-Throughput Experimentation Approach.- Radiopharmaceutical Discovery with 11CO2-Fixation Methods Inspired by Green Chemistry.
