Iridium (I)-Catalyzed Enantioselective Hydroarylation of Alkenes via C-H bond Activation: Experiment and Computation.
Type
ArticleKAUST Department
Chemical Science ProgramKAUST Catalysis Center (KCC)
King Abdullah University of Science and Technology, KAUST Catalysis Center, Landoltweg 1, 23955, Thuwal, SAUDI ARABIA.
Physical Science and Engineering (PSE) Division
Date
2020-06-22Online Publication Date
2020-06-22Print Publication Date
2020-07-02Embargo End Date
2021-04-18Submitted Date
2020-04-15Permanent link to this record
http://hdl.handle.net/10754/662584
Metadata
Show full item recordAbstract
A new catalytic enantioselective hydroarylation of unactivated olefins provides rapid access to functionalized chiral dihydrobenzofurans with good yields and excellent enantio-selectivities. Simple aromatic ketones or amides act as directing group allowing the regioselective reaction at the more hindered ortho position. Tertiary benzylic stereocenters are obtained directly under mild reaction conditions and with complete atom economy from readily available starting materials.Citation
Rueping, M., Shinde, V., Mane, M., & Cavallo, L. (2020). Iridium (I)-Catalyzed Enantioselective Hydroarylation of Alkenes via C–H bond Activation: Experiment and Computation. Chemistry – A European Journal. doi:10.1002/chem.202001793Publisher
WileyJournal
Chemistry – A European JournalPubMed ID
32301132Additional Links
https://onlinelibrary.wiley.com/doi/abs/10.1002/chem.202001793Relations
Is Supplemented By:- [Dataset]
Shinde, Valmik. (2018). CCDC 1877011: Experimental Crystal Structure Determination [Data set]. Cambridge Crystallographic Data Centre. https://doi.org/10.5517/CCDC.CSD.CC2105R0. DOI: 10.5517/ccdc.csd.cc2105r0 Handle: 10754/665102
ae974a485f413a2113503eed53cd6c53
10.1002/chem.202001793
Scopus Count
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