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Volumn 131, Issue 22, 2009, Pages 7502-7503

Easily attachable and detachable ortho-directing agent for arylboronic acids in ruthenium-catalyzed aromatic C-H silylation

Author keywords

[No Author keywords available]

Indexed keywords

ARYLBORONIC ACIDS; BIARYLS; CHEMICAL EQUATIONS; CONDENSATION PRODUCT; GOOD YIELD; HYDROSILANES; IN-SITU; METHOXY; PHENYLBORONIC ACIDS; REGIO-SELECTIVE; SILYLATION; TAMAO OXIDATION; TRIFLUOROMETHYL GROUP; TRIORGANOSILANES;

EID: 67650558689     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja902314v     Document Type: Article
Times cited : (174)

References (34)
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    • (c) Chatani, N., Ed. Directed Metallation; Springer: Berlin, Germany, 2007.
    • (2007) Directed Metallation
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    • Dyker, G., Ed. Wiley-VCH: Weinheim
    • (b) Dyker, G., Ed. Handbook of C-H Transformations; Wiley-VCH: Weinheim, 2005.
    • (2005) Handbook of C-H Transformations
  • 10
    • 0000463307 scopus 로고
    • For earlier pioneering work, see
    • For earlier pioneering work, see: Lewis, L. N.; Smith, J. F. J. Am. Chem. Soc. 1986, 108, 2728.
    • (1986) J. Am. Chem. Soc. , vol.108 , pp. 2728
    • Lewis, L.N.1    Smith, J.F.2
  • 11
    • 0013373107 scopus 로고    scopus 로고
    • For removable directing groups for C-H and C-C activation, see
    • For removable directing groups for C-H and C-C activation, see: (a) Oi, S.; Ogino, Y.; Fukita, S.; Inoue, Y. Org. Lett. 2002, 4, 1783.
    • (2002) Org. Lett. , vol.4 , pp. 1783
    • Oi, S.1    Ogino, Y.2    Fukita, S.3    Inoue, Y.4
  • 18
    • 33750591065 scopus 로고    scopus 로고
    • For use of pyridylmethylsilyl group as a convertible directing group for Heck reactions of vinylsilanes, see
    • For use of pyridylmethylsilyl group as a convertible directing group for Heck reactions of vinylsilanes, see: Itami, K.; Yoshida, J. Bull. Chem. Soc. Jpn. 2006, 79, 811.
    • (2006) Bull. Chem. Soc. Jpn. , vol.79 , pp. 811
    • Itami, K.1    Yoshida, J.2
  • 19
    • 33846792442 scopus 로고    scopus 로고
    • Hall, D. G., Ed.; Wiley: Weinheim
    • Hall, D. G. In Boronic Acid; Hall, D. G., Ed.; Wiley: Weinheim, 2005; p 1.
    • (2005) Boronic Acid , pp. 1
    • Hall, D.G.1
  • 22
    • 67650555364 scopus 로고    scopus 로고
    • 2-Pyrazol-5-ylaniline was prepared via three steps from o-nitroacetophenone in 83% overall yield. See the Supporting Information
    • 2-Pyrazol-5-ylaniline was prepared via three steps from o-nitroacetophenone in 83% overall yield. See the Supporting Information.
  • 23
    • 67650531074 scopus 로고    scopus 로고
    • PhB(pza) showed no decomposition over at least 10 months on storage in a vial in air
    • PhB(pza) showed no decomposition over at least 10 months on storage in a vial in air.
  • 29
    • 67650540734 scopus 로고    scopus 로고
    • Some of the produced B(pin) derivatives were still unstable toward silica gel column chromatography
    • Some of the produced B(pin) derivatives were still unstable toward silica gel column chromatography.
  • 30
    • 67650510626 scopus 로고    scopus 로고
    • Silylation of the benzylic C-H bond proceeded slowly in low yield
    • Silylation of the benzylic C-H bond proceeded slowly in low yield.
  • 31
    • 54749090359 scopus 로고    scopus 로고
    • Nondirected, Ir-catalyzed silylation of thiophenes has been reported
    • Nondirected, Ir-catalyzed silylation of thiophenes has been reported: Lu, B.; Falck, J. R. Angew. Chem., Int. Ed. 2008, 47, 7508.
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 7508
    • Lu, B.1    Falck, J.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.