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Tanji, Yutaka, Hamaguchi, Ryo, Tsuji, Yasushi, Fujihara, Tetsuaki (2020) Pd-Catalyzed intermolecular C–H bond arylation reactions: effect of bulkiness of carboxylate ligands. Chemical Communications, 56 (27) 3843-3846 doi:10.1039/d0cc01129k

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Reference TypeJournal (article/letter/editorial)
TitlePd-Catalyzed intermolecular C–H bond arylation reactions: effect of bulkiness of carboxylate ligands
JournalChemical Communications
AuthorsTanji, YutakaAuthor
Hamaguchi, RyoAuthor
Tsuji, YasushiAuthor
Fujihara, TetsuakiAuthor
Year2020Volume56
Issue27
PublisherRoyal Society of Chemistry (RSC)
DOIdoi:10.1039/d0cc01129kSearch in ResearchGate
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Mindat Ref. ID15469878Long-form Identifiermindat:1:5:15469878:2
GUID0
Full ReferenceTanji, Yutaka, Hamaguchi, Ryo, Tsuji, Yasushi, Fujihara, Tetsuaki (2020) Pd-Catalyzed intermolecular C–H bond arylation reactions: effect of bulkiness of carboxylate ligands. Chemical Communications, 56 (27) 3843-3846 doi:10.1039/d0cc01129k
Plain TextTanji, Yutaka, Hamaguchi, Ryo, Tsuji, Yasushi, Fujihara, Tetsuaki (2020) Pd-Catalyzed intermolecular C–H bond arylation reactions: effect of bulkiness of carboxylate ligands. Chemical Communications, 56 (27) 3843-3846 doi:10.1039/d0cc01129k
In(2020) Chemical Communications Vol. 56 (27) Royal Society of Chemistry (RSC)

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Tanji, Yutaka, Mitsutake, Naoya, Fujihara, Tetsuaki, Tsuji, Yasushi (2018) Steric Effect of Carboxylate Ligands on Pd-Catalyzed Intramolecular C(sp2 )-H and C(sp3 )-H Arylation Reactions. Angewandte Chemie, 130 (32). 10471-10474 doi:10.1002/ange.201804566
Tanji, Yutaka, Mitsutake, Naoya, Fujihara, Tetsuaki, Tsuji, Yasushi (2018) Steric Effect of Carboxylate Ligands on Pd-Catalyzed Intramolecular C(sp2 )-H and C(sp3 )-H Arylation Reactions. Angewandte Chemie International Edition, 57 (32). 10314-10317 doi:10.1002/anie.201804566
Matsuda, Yuki, Tsuji, Yasushi, Fujihara, Tetsuaki (2020) Cu-Catalyzed three-component coupling reactions using nitriles, 1,3-dienes and silylboranes. Chemical Communications, 56 (34) 4648-4651 doi:10.1039/d0cc01803a
Fujihara, Tetsuaki, Yokota, Ken, Terao, Jun, Tsuji, Yasushi (2017) Copper-catalyzed hydroallylation of allenes employing hydrosilanes and allyl chlorides. Chemical Communications, 53 (56). 7898-7900 doi:10.1039/c7cc02816d
Fujihara, Tetsuaki, Yoshikawa, Takahiro, Satou, Motoi, Ohta, Hidetoshi, Terao, Jun, Tsuji, Yasushi (2015) N-Heterocyclic carbene ligands bearing poly(ethylene glycol) chains: effect of the chain length on palladium-catalyzed coupling reactions employing aryl chlorides. Chemical Communications, 51 (98). 17382-17385 doi:10.1039/c5cc07588b
Fujihara, Tetsuaki, Tomike, Yoshikazu, Ohtake, Toshiyuki, Terao, Jun, Tsuji, Yasushi (2011) Ruthenium-catalyzed ring-closing metathesis accelerated by long-range steric effect. Chemical Communications, 47 (34). 9699pp. doi:10.1039/c1cc13304g
Tsuji, Yasushi, Fujihara, Tetsuaki (2012) Carbon dioxide as a carbon source in organic transformation: carbon–carbon bond forming reactions by transition-metal catalysts. Chemical Communications, 48 (80). 9956pp. doi:10.1039/c2cc33848c
Tani, Yosuke, Kuga, Kazunari, Fujihara, Tetsuaki, Terao, Jun, Tsuji, Yasushi (2015) Copper-catalyzed C–C bond-forming transformation of CO2 to alcohol oxidation level: selective synthesis of homoallylic alcohols from allenes, CO2, and hydrosilanes. Chemical Communications, 51 (65). 13020-13023 doi:10.1039/c5cc03932k
Fujihara, Tetsuaki, Katafuchi, Yuko, Iwai, Tomohiro, Terao, Jun, Tsuji, Yasushi (2010) Palladium-Catalyzed Intermolecular Addition of Formamides to Alkynes. Journal Of The American Chemical Society, 132 (6) 2094-2098 doi:10.1021/ja910038p
Fujihara, Tetsuaki, Hosoki, Tomoya, Katafuchi, Yuko, Iwai, Tomohiro, Terao, Jun, Tsuji, Yasushi (2012) Palladium-catalyzed esterification of aryl halides using aryl formates without the use of external carbon monoxide. Chemical Communications, 48 (64). 8012pp. doi:10.1039/c2cc33944g
FUJIHARA, Tetsuaki, TSUJI, Yasushi (2016) Transition Metal-catalyzed Fixation of Carbon Dioxide via Carbon–carbon Bond Formation. Journal of the Japan Petroleum Institute, 59 (3). 84-92 doi:10.1627/jpi.59.84
 
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