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Roberts, Riley A., Metze, Bryan E., Nilova, Aleksandra, Stuart, David R. (2023) Synthesis of Arynes via Formal Dehydrogenation of Arenes. Journal of the American Chemical Society, 145 (6) 3306-3311 doi:10.1021/jacs.2c13007

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Reference TypeJournal (article/letter/editorial)
TitleSynthesis of Arynes via Formal Dehydrogenation of Arenes
JournalJournal of the American Chemical Society
AuthorsRoberts, Riley A.Author
Metze, Bryan E.Author
Nilova, AleksandraAuthor
Stuart, David R.Author
Year2023 (February 15)Volume145
Issue6
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/jacs.2c13007Search in ResearchGate
Generate Citation Formats
Mindat Ref. ID15706746Long-form Identifiermindat:1:5:15706746:2
GUID0
Full ReferenceRoberts, Riley A., Metze, Bryan E., Nilova, Aleksandra, Stuart, David R. (2023) Synthesis of Arynes via Formal Dehydrogenation of Arenes. Journal of the American Chemical Society, 145 (6) 3306-3311 doi:10.1021/jacs.2c13007
Plain TextRoberts, Riley A., Metze, Bryan E., Nilova, Aleksandra, Stuart, David R. (2023) Synthesis of Arynes via Formal Dehydrogenation of Arenes. Journal of the American Chemical Society, 145 (6) 3306-3311 doi:10.1021/jacs.2c13007
In(2023, February) Journal Of The American Chemical Society Vol. 145 (6) American Chemical Society (ACS)

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Metze, Bryan E., Roberts, Riley A., Nilova, Aleksandra, Stuart, David R. (2023) An efficient and chemoselective method to generate arynes. Chemical Science, 14 (47) 13885-13892 doi:10.1039/d3sc05429b
Roberts, Riley A., Metze, Bryan E., Javaly, Nicole, McCormick, Theresa M., Stuart, David R. (2025) Access to arynes from arenes via net dehydrogenation: scope, synthetic applications and mechanistic analysis. Chemical Science, 16 (13). doi:10.1039/d5sc00054h
Karandikar, Shubhendu S., Metze, Bryan E., Roberts, Riley A., Stuart, David R. (2023) Oxidative Cycloaddition Reactions of Arylboron Reagents via a One-pot Formal Dehydroboration Sequence. Organic Letters, 25 (34) 6374-6379 doi:10.1021/acs.orglett.3c02379
Nilova, Aleksandra, Metze, Bryan, Stuart, David R. (2021) Aryl(TMP)iodonium Tosylate Reagents as a Strategic Entry Point to Diverse Aryl Intermediates: Selective Access to Arynes. Organic Letters, 23 (12) 4813-4817 doi:10.1021/acs.orglett.1c01534
Nilova, Aleksandra, Sibbald, Paul A., Valente, Edward J., González‐Montiel, Gisela A., Richardson, H. Camille, Brown, Kevin S., Cheong, Paul Ha‐Yeon, Stuart, David R. (2021) Regioselective Synthesis of 1,2,3,4‐Tetrasubstituted Arenes by Vicinal Functionalization of Arynes Derived from Aryl(Mes)iodonium Salts**. Chemistry – A European Journal, 27 (24) 7168-7175 doi:10.1002/chem.202100201
Nguyen, Vu, GrĂźnwald, Michael (2018) Microscopic Origins of Poor Crystallinity in the Synthesis of Covalent Organic Framework COF-5. Journal Of The American Chemical Society, 140 (9) 3306-3311 doi:10.1021/jacs.7b12529
Sundalam, Sunil K., Nilova, Aleksandra, Seidl, Thomas L., Stuart, David R. (2016) A Selective C−H Deprotonation Strategy to Access Functionalized Arynes by Using Hypervalent Iodine. Angewandte Chemie, 128 (29). 8571-8574 doi:10.1002/ange.201603222
Sundalam, Sunil K., Nilova, Aleksandra, Seidl, Thomas L., Stuart, David R. (2016) A Selective C−H Deprotonation Strategy to Access Functionalized Arynes by Using Hypervalent Iodine. Angewandte Chemie International Edition, 55 (29). 8431-8434 doi:10.1002/anie.201603222
Liu, Xing-Yu, Cai, Wei, Ronceray, Nathan, Radenovic, Aleksandra, Fierz, Beat, Waser, Jerome (2023) Synthesis of Fluorescent Cyclic Peptides via Gold(I)-Catalyzed Macrocyclization. Journal of the American Chemical Society, 145 (49) 26525-26531 doi:10.1021/jacs.3c09261
Meng, Guangrong, Hu, Liang, Chan, Hau Sun Sam, Qiao, Jennifer X., Yu, Jin-Quan (2023) Synthesis of 1,3-Dienes via Ligand-Enabled Sequential Dehydrogenation of Aliphatic Acids. Journal of the American Chemical Society, 145 (24) 13003-13007 doi:10.1021/jacs.3c03378
Sheng, Tao, Kang, Guowei, Zhuang, Zhe, Chekshin, Nikita, Wang, Zhen, Hu, Liang, Yu, Jin-Quan (2023) Synthesis of β,γ-Unsaturated Aliphatic Acids via Ligand-Enabled Dehydrogenation. Journal of the American Chemical Society, 145 (38) 20951-20958 doi:10.1021/jacs.3c06423
 
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