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Volumn 17, Issue 19, 2015, Pages 4674-4677

Beyond Directed ortho Metalation: Ruthenium-Catalyzed Amide-Directed CAr-OMe Activation/Cross-Coupling Reaction of Naphthamides with Aryl Boronates

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EID: 84942916134     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/acs.orglett.5b01913     Document Type: Article
Times cited : (38)

References (34)
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    • Report of direct aryl ether/aryl Bneop coupling reaction under Ni-catalyzed conditions that is compromised by the low reactivity of the substrate anisoles and the requirement of a large excess of base (CsF)
    • Report of direct aryl ether/aryl Bneop coupling reaction under Ni-catalyzed conditions that is compromised by the low reactivity of the substrate anisoles and the requirement of a large excess of base (CsF): Tobisu, M.; Shimasaki, T.; Chatani, N. Angew. Chem., Int. Ed. 2008, 47, 4866 10.1002/anie.200801447
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 4866
    • Tobisu, M.1    Shimasaki, T.2    Chatani, N.3
  • 11
    • 0003469129 scopus 로고
    • The amide group exhibits greater coordinating ability than the ketone group; see: 16 th ed. Longman: New York.
    • The amide group exhibits greater coordinating ability than the ketone group; see: Kaye, G. W. C.; Laby, T. H. Tables of Physical and Chemical Constants, 16 th ed.; Longman: New York, 1995.
    • (1995) Tables of Physical and Chemical Constants
    • Kaye, G.W.C.1    Laby, T.H.2
  • 17
    • 0012397313 scopus 로고
    • Snieckus, V. Chem. Rev. 1990, 90, 879 10.1021/cr00104a001
    • (1990) Chem. Rev. , vol.90 , pp. 879
    • Snieckus, V.1
  • 20
    • 84942913145 scopus 로고    scopus 로고
    • Ph.D. Thesis, Queen's University, Kingston, Ontario, Canada.
    • Zhao, Y. Ph.D. Thesis, Queen's University, Kingston, Ontario, Canada, 2010.
    • (2010)
    • Zhao, Y.1
  • 21
    • 84942873189 scopus 로고    scopus 로고
    • See Supporting Information.
    • See Supporting Information.
  • 22
    • 84903220099 scopus 로고    scopus 로고
    • Arylboronic acid and its pinacol ester were tested in our Ru-catalyzed amide-directed C-N activation/coupling chemistry (see ref 12a and
    • Arylboronic acid and its pinacol ester were tested in our Ru-catalyzed amide-directed C-N activation/coupling chemistry (see ref 12a and Zhao, Y.; Snieckus, V. Org. Lett. 2014, 16, 3200 10.1021/ol501180q
    • (2014) Org. Lett. , vol.16 , pp. 3200
    • Zhao, Y.1    Snieckus, V.2
  • 23
    • 84942889769 scopus 로고    scopus 로고
    • In amide-directed C-OMe activation/coupling reactions, use of pinacolone as a solvent afforded low yields of products.
    • In amide-directed C-OMe activation/coupling reactions, use of pinacolone as a solvent afforded low yields of products.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.