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Kamitani, Miharu, Nakayasu, Bunta, Fujimoto, Hayato, Yasui, Kosuke, Kodama, Takuya, Tobisu, Mamoru (2023) Single–carbon atom transfer to α,β-unsaturated amides from N-heterocyclic carbenes. Science, 379 (6631) 484-488 doi:10.1126/science.ade5110

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Reference TypeJournal (article/letter/editorial)
TitleSingle–carbon atom transfer to α,β-unsaturated amides from N-heterocyclic carbenes
JournalScience
AuthorsKamitani, MiharuAuthor
Nakayasu, BuntaAuthor
Fujimoto, HayatoAuthor
Yasui, KosukeAuthor
Kodama, TakuyaAuthor
Tobisu, MamoruAuthor
Year2023 (February 3)Volume379
Issue6631
PublisherAmerican Association for the Advancement of Science (AAAS)
DOIdoi:10.1126/science.ade5110Search in ResearchGate
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Mindat Ref. ID15693696Long-form Identifiermindat:1:5:15693696:7
GUID0
Full ReferenceKamitani, Miharu, Nakayasu, Bunta, Fujimoto, Hayato, Yasui, Kosuke, Kodama, Takuya, Tobisu, Mamoru (2023) Single–carbon atom transfer to α,β-unsaturated amides from N-heterocyclic carbenes. Science, 379 (6631) 484-488 doi:10.1126/science.ade5110
Plain TextKamitani, Miharu, Nakayasu, Bunta, Fujimoto, Hayato, Yasui, Kosuke, Kodama, Takuya, Tobisu, Mamoru (2023) Single–carbon atom transfer to α,β-unsaturated amides from N-heterocyclic carbenes. Science, 379 (6631) 484-488 doi:10.1126/science.ade5110
In(2023, February) Science Vol. 379 (6631) American Association for the Advancement of Science (AAAS)

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Yasui, Kosuke, Kamitani, Miharu, Tobisu, Mamoru (2019) N‐Heterocyclic Carbene Catalyzed Concerted Nucleophilic Aromatic Substitution of Aryl Fluorides Bearing α,β‐Unsaturated Amides. Angewandte Chemie, 131 (40). 14295-14299 doi:10.1002/ange.201907837
Yasui, Kosuke, Kamitani, Miharu, Tobisu, Mamoru (2019) N‐Heterocyclic Carbene Catalyzed Concerted Nucleophilic Aromatic Substitution of Aryl Fluorides Bearing α,β‐Unsaturated Amides. Angewandte Chemie International Edition, 58 (40). 14157-14161 doi:10.1002/anie.201907837
Yasui, Kosuke, Kamitani, Miharu, Fujimoto, Hayato, Tobisu, Mamoru (2021) N-Heterocyclic Carbene-Catalyzed Truce–Smiles Rearrangement of N-Arylacrylamides via the Cleavage of Unactivated C(aryl)–N Bonds. Organic Letters, 23 (5) 1572-1576 doi:10.1021/acs.orglett.0c04281
Fujimoto, Hayato, Nakayasu, Bunta, Tobisu, Mamoru (2023) Synthesis of γ-Lactams from Acrylamides by Single-Carbon Atom Doping Annulation. Journal of the American Chemical Society, 145 (36) 19518-19522 doi:10.1021/jacs.3c07052
Yasui, Kosuke, Kamitani, Miharu, Fujimoto, Hayato, Tobisu, Mamoru (2020) The Effect of the Leaving Group in N-Heterocyclic Carbene-Catalyzed Nucleophilic Aromatic Substitution Reactions. Bulletin of the Chemical Society of Japan, 93 (12) 1424-1429 doi:10.1246/bcsj.20200210
Fujimoto, Hayato, Yasui, Kosuke, Tobisu, Mamoru (2023) Non-Classical Molecular Activation by Phosphines and N-Heterocyclic Carbenes and Its Application to Catalytic Reactions. Bulletin of the Chemical Society of Japan, 96 (9) 872-886 doi:10.1246/bcsj.20230150
Fujimoto, Hayato, Kusano, Momoka, Kodama, Takuya, Tobisu, Mamoru (2019) Cyclization of Bisphosphines to Phosphacycles via the Cleavage of Two Carbon–Phosphorus Bonds by Nickel Catalysis. Organic Letters, 21. 4177-4181 doi:10.1021/acs.orglett.9b01355
Fujimoto, Hayato, Kusano, Momoka, Kodama, Takuya, Tobisu, Mamoru (2020) Aryne-Induced SNAr/Dearylation Strategy for the Synthesis of Fluorinated Dibenzophospholes from Triarylphosphines via a P(V) Intermediate. Organic Letters, 22. 2293-2297 doi:10.1021/acs.orglett.0c00489
Fujimoto, Hayato, Nishioka, Teruki, Imachi, Kazuya, Ogawa, Satoshi, Nishimura, Rio, Tobisu, Mamoru (2025) Generation of Stereocenters via Single-Carbon-Atom Doping Using N-Isocyanides. Journal of the American Chemical Society, 147 (10). doi:10.1021/jacs.5c00882
Fujimoto, Hayato, Kodama, Takuya, Yamanaka, Masahiro, Tobisu, Mamoru (2020) Phosphine-Catalyzed Intermolecular Acylfluorination of Alkynes via a P(V) Intermediate. Journal of the American Chemical Society, 142 (41) 17323-17328 doi:10.1021/jacs.0c08928
Zhu, Kaige, Kamochi, Kosuke, Kodama, Takuya, Tobisu, Mamoru, Amaya, Toru (2020) Chiral cyclic [n]spirobifluorenylenes: carbon nanorings consisting of helically arranged quaterphenyl rods illustrating partial units of woven patterns. Chemical Science, 11 (35) 9604-9610 doi:10.1039/d0sc02452j
 
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