Litcius/Paper detail

The Chosen Few: Parallel Library Reaction Methodologies for Drug Discovery

Amanda W. Dombrowski, Ana L. Aguirre, Anurupa Shrestha, Kathy Sarris, Ying Wang

2021The Journal of Organic Chemistry92 citationsDOI

Abstract

Parallel library synthesis is an important tool for drug discovery because it enables the synthesis of closely related analogues in parallel via robust and general synthetic transformations. In this perspective, we analyzed the synthetic methodologies used in >5000 parallel libraries representing 15 prevalent synthetic transformations. The library data set contains complex substrates and diverse arrays of building blocks used over the last 14 years at AbbVie. The library synthetic methodologies that have demonstrated robustness and generality with proven success are described along with their substrate scopes. The evolution of the synthetic methodologies for library synthesis over the past decade is discussed. We also highlight that the combination of parallel library synthesis with high-throughput experimentation will continue to facilitate the discovery of library-amenable synthetic methodologies in drug discovery.

Topics & Concepts

Drug discoveryGeneralityComputer scienceRobustness (evolution)Combinatorial chemistryChemistryBiochemistryPsychologyPsychotherapistGeneChemical Synthesis and AnalysisInnovative Microfluidic and Catalytic Techniques InnovationClick Chemistry and Applications
The Chosen Few: Parallel Library Reaction Methodologies for Drug Discovery | Litcius