Radicals in natural product synthesis.

Chem Soc Rev

Department of Chemistry, University of Michigan, 930 N. University Ave, Ann Arbor, MI 48109, USA.

Published: October 2018

Free radical intermediates have intrigued chemists since their discovery, and an ever-increasing appreciation for their unique reactivity has resulted in the widespread utilization of these species throughout the field of chemical synthesis. This is most evident from the recent surge in the application of intermolecular radical reactions that feature in complex molecule syntheses. This tutorial review will discuss the diverse methods utilized for radical generation and reactivity to form critical bonds in natural product total synthesis. In particular, stabilized (e.g. benzyl) and persistent (e.g. TEMPO) radicals will be the primary focus.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6205920PMC
http://dx.doi.org/10.1039/c8cs00379cDOI Listing

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