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Reichert, Elaine C., Feng, Kaibo, Sather, Aaron C., Buchwald, Stephen L. (2023) Pd-Catalyzed Amination of Base-Sensitive Five-Membered Heteroaryl Halides with Aliphatic Amines. Journal of the American Chemical Society, 145 (6) 3323-3329 doi:10.1021/jacs.2c13520

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Reference TypeJournal (article/letter/editorial)
TitlePd-Catalyzed Amination of Base-Sensitive Five-Membered Heteroaryl Halides with Aliphatic Amines
JournalJournal of the American Chemical Society
AuthorsReichert, Elaine C.Author
Feng, KaiboAuthor
Sather, Aaron C.Author
Buchwald, Stephen L.Author
Year2023 (February 15)Volume145
Issue6
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/jacs.2c13520Search in ResearchGate
Generate Citation Formats
Mindat Ref. ID15706771Long-form Identifiermindat:1:5:15706771:4
GUID0
Full ReferenceReichert, Elaine C., Feng, Kaibo, Sather, Aaron C., Buchwald, Stephen L. (2023) Pd-Catalyzed Amination of Base-Sensitive Five-Membered Heteroaryl Halides with Aliphatic Amines. Journal of the American Chemical Society, 145 (6) 3323-3329 doi:10.1021/jacs.2c13520
Plain TextReichert, Elaine C., Feng, Kaibo, Sather, Aaron C., Buchwald, Stephen L. (2023) Pd-Catalyzed Amination of Base-Sensitive Five-Membered Heteroaryl Halides with Aliphatic Amines. Journal of the American Chemical Society, 145 (6) 3323-3329 doi:10.1021/jacs.2c13520
In(2023, February) Journal Of The American Chemical Society Vol. 145 (6) American Chemical Society (ACS)

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Raguram, Elaine Reichert, Dahl, Jakob C., Jensen, Klavs F., Buchwald, Stephen L. (2024) Kinetic Modeling Enables Understanding of Off-Cycle Processes in Pd-Catalyzed Amination of Five-Membered Heteroaryl Halides. Journal of the American Chemical Society, 146 (48). doi:10.1021/jacs.4c10488
Feng, Kaibo, Raguram, Elaine Reichert, Howard, James R., Peters, Ellyn, Liu, Cecilia, Sigman, Matthew S., Buchwald, Stephen L. (2024) Development of a Deactivation-Resistant Dialkylbiarylphosphine Ligand for Pd-Catalyzed Arylation of Secondary Amines. Journal of the American Chemical Society, 146 (39). doi:10.1021/jacs.4c09667
Charles, Mark D., Schultz, Phillip, Buchwald, Stephen L. (2005) Efficient Pd-Catalyzed Amination of Heteroaryl Halides. Organic Letters, 7. 3965-3968 doi:10.1021/ol0514754
McCann, Scott D., Reichert, Elaine C., Arrechea, Pedro Luis, Buchwald, Stephen L. (2020) Development of an Aryl Amination Catalyst with Broad Scope Guided by Consideration of Catalyst Stability. Journal of the American Chemical Society, 142 (35) 15027-15037 doi:10.1021/jacs.0c06139
Sather, Aaron C., Lee, Hong Geun, De La Rosa, Valentina Y., Yang, Yang, Müller, Peter, Buchwald, Stephen L. (2015) A Fluorinated Ligand Enables Room-Temperature and Regioselective Pd-Catalyzed Fluorination of Aryl Triflates and Bromides. Journal Of The American Chemical Society, 137 (41) 13433-13438 doi:10.1021/jacs.5b09308
Zhou, Fabin, Zhang, Lixue, Hu, Wenbo, Yuan, Bingxin, Shi, Ji-cheng (2023) A general catalyst for Buchwald-Hartwig amination to prepare secondary five-membered heteroaryl amines with breaking the base barrier. Journal of Catalysis, 422. 36-42 doi:10.1016/j.jcat.2023.02.018
Li, Mingda, Jin, Yangbin, Chen, Yupeng, Wu, Wanqing, Jiang, Huanfeng (2023) Palladium-Catalyzed Oxidative Amination of Unactivated Olefins with Primary Aliphatic Amines. Journal of the American Chemical Society, 145 (17) 9448-9453 doi:10.1021/jacs.3c02114
Kim, Seoung-Tae, Strauss, Michael J., Cabré, Albert, Buchwald, Stephen L. (2023) Room-Temperature Cu-Catalyzed Amination of Aryl Bromides Enabled by DFT-Guided Ligand Design. Journal of the American Chemical Society, 145 (12) 6966-6975 doi:10.1021/jacs.3c00500
Su, Mingjuan, Hoshiya, Naoyuki, Buchwald, Stephen L. (2014) Palladium-Catalyzed Amination of Unprotected Five-Membered Heterocyclic Bromides. Organic Letters, 16. 832-835 doi:10.1021/ol4035947
Huang, Xiaohua, Buchwald, Stephen L. (2001) New Ammonia Equivalents for the Pd-Catalyzed Amination of Aryl Halides. Organic Letters, 3. 3417-3419 doi:10.1021/ol0166808
Milner, Phillip J., Yang, Yang, Buchwald, Stephen L. (2015) In-Depth Assessment of the Palladium-Catalyzed Fluorination of Five-Membered Heteroaryl Bromides. Organometallics, 34. 4775-4780 doi:10.1021/acs.organomet.5b00631
 
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