Abstract
This chapter focuses on the exploration and application of cascade reactions in the total synthesis of both biologically active natural products and their analogues and synthetic substances for drug discovery. The high synthetic efficiency of such processes enables the facile and rapid construction of bioactive molecules and furthermore streamlines the study of structure-activity relationships to accelerate the identification of potential drug-like compounds for further biological evaluation. In addition, the power of cascade strategies is also demonstrated in the pilot plant-scale synthesis of highly valued, structurally complex drugs and drug candidates.
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The financial support from the NSF (CHE-1057569) is gratefully acknowledged.
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Yu, C., Huang, H., Sheng, C., Wang, W. (2022). Designing Efficient Cascade Reactions in Drug Discovery. In: Richardson, P.F. (eds) Green Chemistry in Drug Discovery. Methods in Pharmacology and Toxicology. Humana, New York, NY. https://doi.org/10.1007/978-1-0716-1579-9_7
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