The medicinal chemist's toolbox for late stage functionalization of drug-like molecules
Merck & Co., Inc., Rahway, NJ, USA (United States) · Merck Institute for Science Education
Abstract
The advent of modern C-H functionalization chemistries has enabled medicinal chemists to consider a synthetic strategy, late stage functionalization (LSF), which utilizes the C-H bonds of drug leads as points of diversification for generating new analogs. LSF approaches offer the promise of rapid exploration of structure activity relationships (SAR), the generation of oxidized metabolites, the blocking of metabolic hot spots and the preparation of biological probes. This review details a toolbox of intermolecular C-H functionalization chemistries with proven applicability to drug-like molecules, classified by regioselectivity patterns, and gives guidance on how to systematically develop LSF strategies using…
Citation impact
- FWCI
- 52.82
- Percentile
- 100%
- References
- 277
Authors
5- TCTim CernakCorresponding
Merck & Co., Inc., Rahway, NJ, USA (United States)
- KDKevin D. Dykstra
Merck & Co., Inc., Rahway, NJ, USA (United States), Merck Institute for Science Education
- STSriram Tyagarajan
Merck & Co., Inc., Rahway, NJ, USA (United States), Merck Institute for Science Education
- PVPetr Váchal
Merck & Co., Inc., Rahway, NJ, USA (United States), Merck Institute for Science Education
- SWShane W. Krska
Merck & Co., Inc., Rahway, NJ, USA (United States), Merck Institute for Science Education
Topics & keywords
- Surface modification
- Toolbox
- Chemist
- Chemistry
- Combinatorial chemistry
- Nanotechnology
- Computer science
- Organic chemistry