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Volumn 13, Issue 12, 2011, Pages 3076-3079

Copper-mediated annulative direct coupling of o -alkynylphenols with oxadiazoles: A dehydrogenative cascade construction of biheteroaryls

Author keywords

[No Author keywords available]

Indexed keywords

ALKYNE; COPPER; OXADIAZOLE DERIVATIVE; PHENOL DERIVATIVE;

EID: 79958821042     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol200975j     Document Type: Article
Times cited : (44)

References (86)
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    • For selected recent examples, see
    • For selected recent examples, see: Do, H.-Q.; Daugulis, O. J. Am. Chem. Soc. 2007, 129, 12404
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    • Do, H.-Q.1    Daugulis, O.2
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    • 33744786786 scopus 로고    scopus 로고
    • For copper-mediated direct functionalization of arylazines, see
    • For copper-mediated direct functionalization of arylazines, see: Chen, X.; Hao, X.-S.; Goodhue, C. E.; Yu, J.-Q. J. Am. Chem. Soc. 2006, 128, 6790
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 6790
    • Chen, X.1    Hao, X.-S.2    Goodhue, C.E.3    Yu, J.-Q.4
  • 57
    • 51049114031 scopus 로고    scopus 로고
    • For reviews of metal-mediated annulation of o -alkynylphenols and -anilines, see
    • For reviews of metal-mediated annulation of o -alkynylphenols and -anilines, see: Patil, N. T.; Yamamoto, Y Chem. Rev. 2008, 108, 3395
    • (2008) Chem. Rev. , vol.108 , pp. 3395
    • Patil, N.T.1    Yamamoto, Y.2
  • 82
    • 79958791883 scopus 로고    scopus 로고
    • 2 dropped the yield to 8% and 21% yields, respectively
    • 2 dropped the yield to 8% and 21% yields, respectively.
  • 83
    • 35848934578 scopus 로고    scopus 로고
    • 2 for an oxidation of Cu(I) into Cu(II)
    • 2 for an oxidation of Cu(I) into Cu(II): Zhang, W.; Chemler, S. R. J. Am. Chem. Soc. 2007, 129, 12948
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 12948
    • Zhang, W.1    Chemler, S.R.2
  • 85
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    • 2, the product was not obtained at all. Under 5 mol % catalyst loading, 3aa was formed in 10% yield (GC)
    • 2, the product was not obtained at all. Under 5 mol % catalyst loading, 3aa was formed in 10% yield (GC).
  • 86
    • 79958823083 scopus 로고    scopus 로고
    • Under the present conditions, attempts to apply aniline analogues, benzoxazole, or benzothiazole were unsuccessful. Further optimization and details will be reported in due course
    • Under the present conditions, attempts to apply aniline analogues, benzoxazole, or benzothiazole were unsuccessful. Further optimization and details will be reported in due course.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.