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Volumn 131, Issue 5, 2009, Pages 1668-1669

Metal-free oxidative cross-coupling of unfunctionalized aromatic compounds

Author keywords

[No Author keywords available]

Indexed keywords

INDUSTRIAL CHEMICALS; IODINE;

EID: 67849129077     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja808940n     Document Type: Article
Times cited : (281)

References (25)
  • 2
    • 34547960227 scopus 로고    scopus 로고
    • Recent reports: (a) Dwight, T. A.; Rue, N. R.; Charvk, D.; Josselvn, R.; DeBoef, B. Org. Lett. 2007, 9, 3137.
    • Recent reports: (a) Dwight, T. A.; Rue, N. R.; Charvk, D.; Josselvn, R.; DeBoef, B. Org. Lett. 2007, 9, 3137.
  • 8
    • 0025174975 scopus 로고    scopus 로고
    • II: (a) Hovorka, M.; Gunterova, J.; Zavada, J. Tetrahedron Lett. 1990, 31, 413.
    • II: (a) Hovorka, M.; Gunterova, J.; Zavada, J. Tetrahedron Lett. 1990, 31, 413.
  • 11
    • 34547218893 scopus 로고    scopus 로고
    • Oxidative cross-coupling of anilines: Jean, A.; Cantat, J.; Bérard, D.; Bouchu, D.; Canesi, S. Qrg. Lett. 2007, 9, 2553.
    • Oxidative cross-coupling of anilines: Jean, A.; Cantat, J.; Bérard, D.; Bouchu, D.; Canesi, S. Qrg. Lett. 2007, 9, 2553.
  • 12
    • 84891738863 scopus 로고    scopus 로고
    • Aromatic cation radical-mediated approach: Dohi. T.; Ito. M.: Morimoto. K.; Iwata, M.; Kita, Y. Angew. Chem., Int. Ed. 2008, 47, 1301.
    • Aromatic cation radical-mediated approach: Dohi. T.; Ito. M.: Morimoto. K.; Iwata, M.; Kita, Y. Angew. Chem., Int. Ed. 2008, 47, 1301.
  • 14
    • 0035819291 scopus 로고    scopus 로고
    • 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
    • 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.
  • 18
    • 0013167416 scopus 로고    scopus 로고
    • Witth, T, Ed, Springer-Verlag: Berlin. Heidelberg
    • (b) Hypervalent Iodine Chemistry; Witth, T., Ed.: Springer-Verlag: Berlin. Heidelberg, 2003.
    • (2003) Hypervalent Iodine Chemistry
  • 20
    • 84891737934 scopus 로고    scopus 로고
    • These regiocontrolled bithiophenes are considered to be versatile synthetic precursors for useful regioregular a-linked polymers
    • These regiocontrolled bithiophenes are considered to be versatile synthetic precursors for useful regioregular a-linked polymers:
  • 24
    • 84891738475 scopus 로고    scopus 로고
    • 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
    • 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.
  • 25
    • 84891736860 scopus 로고    scopus 로고
    • 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
    • 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).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.