Advances in allylic and benzylic C–H bond functionalization enabled by metallaphotoredox catalysis
Type
ArticleKAUST Department
KAUST Catalysis Center (KCC)Chemical Science Program
Physical Science and Engineering (PSE) Division
KAUST Grant Number
URF/1/4384Date
2022Online Publication Date
2021-12-06Permanent link to this record
http://hdl.handle.net/10754/673992
Metadata
Show full item recordAbstract
Metallaphoto-catalysis has been established as a robust platform for efficient construction of a range of chemical bonds. Moreover, transformation of native functionalities such as C(sp3)–H bonds to produce functional molecules represents one of the most attractive strategies in organic synthesis. Merging two powerful methodologies, metallaphoto-catalyzed benzylic and allylic C(sp3)–H bond functionalizations provide a series of general and mild approaches for diversification of alkylbenzenes and alkenes.Citation
Yue, H., Zhu, C., Huang, L., Dewanji, A., & Rueping, M. (2022). Advances in allylic and benzylic C–H bond functionalization enabled by metallaphotoredox catalysis. Chemical Communications. doi:10.1039/d1cc06285aSponsors
This work was financially supported by the King Abdullah University of Science and Technology (KAUST), Saudi Arabia, Office of Sponsored Research (URF/1/4384).Publisher
Royal Society of Chemistry (RSC)Journal
Chemical CommunicationsAdditional Links
http://xlink.rsc.org/?DOI=D1CC06285Aae974a485f413a2113503eed53cd6c53
10.1039/d1cc06285a