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Volumn 130, Issue 24, 2008, Pages 7534-7535

Silyl-directed, iridium-catalyzed ortho-borylation of arenes. A one-pot ortho-borylation of phenols, arylamines, and alkylarenes

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC AMINE; IRIDIUM; PHENOL DERIVATIVE; POLYCYCLIC AROMATIC HYDROCARBON; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE;

EID: 45249114139     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja8015878     Document Type: Article
Times cited : (293)

References (22)
  • 9
    • 45249095719 scopus 로고    scopus 로고
    • Added HBpin has been shown to help generate the active triboryliridium catalyst. See ref 5
    • Added HBpin has been shown to help generate the active triboryliridium catalyst. See ref 5.
  • 15
    • 45249091340 scopus 로고    scopus 로고
    • 2 resulted in no reaction.
    • 2 resulted in no reaction.
  • 16
    • 45249109872 scopus 로고    scopus 로고
    • Substrates containing a single atom between silicon and the arene proved to be more reactive than those with longer linkers. The silyl ether formed from benzyl alcohol did not undergo a similar ortho-borylation
    • Substrates containing a single atom between silicon and the arene proved to be more reactive than those with longer linkers. The silyl ether formed from benzyl alcohol did not undergo a similar ortho-borylation.
  • 18
    • 45249119858 scopus 로고    scopus 로고
    • 3].
    • 3].
  • 19
    • 45249107154 scopus 로고    scopus 로고
    • 8 with HBpin results in non-selective H/D exchange. See Supporting Information.
    • 8 with HBpin results in non-selective H/D exchange. See Supporting Information.
  • 20
    • 0345733884 scopus 로고    scopus 로고
    • This C-H bond activation and C-B bond formation could occur by oxidative addition and reduction or by σ bond metathesis. For calculations on an oxidative addition pathway, see: Tamura, H, Yamazaki, H, Sato, H, Sakaki, S. J. Am. Chem. Soc. 2003, 125, 16114
    • (a) This C-H bond activation and C-B bond formation could occur by oxidative addition and reduction or by σ bond metathesis. For calculations on an oxidative addition pathway, see: Tamura, H.; Yamazaki, H.; Sato, H.; Sakaki, S. J. Am. Chem. Soc. 2003, 125, 16114.
  • 21
    • 0037471658 scopus 로고    scopus 로고
    • For evidence of σ bond metathesis in related C-H borylations, see: b
    • For evidence of σ bond metathesis in related C-H borylations, see: (b) Webster, C. E.; Fan, Y.; Hall, M. B.; Kunz, D.; Hartwig, J. F. J. Am. Chem. Soc. 2003, 125, 858.
    • (2003) J. Am. Chem. Soc , vol.125 , pp. 858
    • Webster, C.E.1    Fan, Y.2    Hall, M.B.3    Kunz, D.4    Hartwig, J.F.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.