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Oxidative cross-coupling of anilines: Jean, A.; Cantat, J.; Bérard, D.; Bouchu, D.; Canesi, S. Qrg. Lett. 2007, 9, 2553.
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Aromatic cation radical-mediated approach: Dohi. T.; Ito. M.: Morimoto. K.; Iwata, M.; Kita, Y. Angew. Chem., Int. Ed. 2008, 47, 1301.
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It should be noted that the previously reported aromatic cation radical- mediated approaches are not suitable for this type of cross-coupling reactions: (a) Tohma, Ft, Morioka, Ft, Takizawa. S, Arisawa, M, Kita. Y. Tetrahedron 2001, 57, 345
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It should be noted that the previously reported aromatic cation radical- mediated approaches are not suitable for this type of cross-coupling reactions: (a) Tohma, Ft.; Morioka, Ft.; Takizawa. S.; Arisawa, M.: Kita. Y. Tetrahedron 2001, 57, 345.
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Hypervalent Iodine Chemistry
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20
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84891737934
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These regiocontrolled bithiophenes are considered to be versatile synthetic precursors for useful regioregular a-linked polymers
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These regiocontrolled bithiophenes are considered to be versatile synthetic precursors for useful regioregular a-linked polymers:
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0344305688
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(a) Zotti, G.; Zecchin, S.; Schiavon, G.: Vercelli, B.; Berlin, A.; Dalcanale. E.; Groenendaal. L. B. Chem. Mater. 2003, 15, 4642.
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Perepichka, D.F.2
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84891738475
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We have confirmed that the addition of several Lewis acids such as TMSOTf or TMSBr could accelerate the reaction of 4c-Br with the arene nucleophile 2b, On the other hand, treatment of the corresponding 4e-OTs with 2b did not react even in the presence of these Lewis acids
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We have confirmed that the addition of several Lewis acids such as TMSOTf or TMSBr could accelerate the reaction of 4c-Br with the arene nucleophile 2b, On the other hand, treatment of the corresponding 4e-OTs with 2b did not react even in the presence of these Lewis acids.
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25
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84891736860
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We have checked the exchange process between the OTs and Br using 4c-OTs by treatment with 1 equiv of TMSBr in HHP 4c-Br: 79% isolated yield
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We have checked the exchange process between the OTs and Br using 4c-OTs by treatment with 1 equiv of TMSBr in HHP (4c-Br: 79% isolated yield).
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