期刊
CHEMICAL SOCIETY REVIEWS
卷 47, 期 21, 页码 7851-7866出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c8cs00379c
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资金
- NIH-NIGMS [GM121656]
- Camille Dreyfus Teacher-Scholar Award Program
- University of Michigan
- National Science Foundation Graduate Research Fellowship [DGE 1256260]
- NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM121656] Funding Source: NIH RePORTER
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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