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Volumn 46, Issue 36, 2010, Pages 6849-6851

A highly adaptable catalyst/substrate system for the synthesis of substituted chromenes

Author keywords

[No Author keywords available]

Indexed keywords

CHROMENE DERIVATIVE; PHENOL DERIVATIVE;

EID: 77956302216     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/c0cc01961e     Document Type: Article
Times cited : (63)

References (42)
  • 2
    • 84944049928 scopus 로고
    • Ed., A. R. Katritzky, C. W. Rees, A. J. Boulton and A. McKillop, Pergamon Press, Oxford
    • J. D. Hepworth, in Comprehensive Heterocyclic Chemistry, ed., A. R. Katritzky, C. W. Rees, A. J. Boulton, and, A. McKillop, Pergamon Press, Oxford, 1984, vol. 3, pp. 737-883
    • (1984) Comprehensive Heterocyclic Chemistry , pp. 737-883
    • Hepworth, J.D.1
  • 3
    • 84906434208 scopus 로고    scopus 로고
    • ed. A. R. Katritzky, C. A. Ramsden, E. F. V. Scriven and R. J. K. Taylor, Elsevier Ltd, Oxford, and previous editions of this series
    • For reviews on chromene synthesis see: M. A. Brimble, J. S. Gibson and J. Sperry, in Comprehensive Heterocyclic Chemistry III, ed., A. R. Katritzky, C. A. Ramsden, E. F. V. Scriven, and, R. J. K. Taylor, Elsevier Ltd, Oxford, 2008, vol. 7, pp. 419-699 and previous editions of this series
    • (2008) Comprehensive Heterocyclic Chemistry III , pp. 419-699
    • Brimble, M.A.1    Gibson, J.S.2    Sperry, J.3
  • 4
    • 77954892711 scopus 로고    scopus 로고
    • ed. A. R. Katritzky, C. A. Ramsden, E. F. V. Scriven and R. J. K. Taylor, Elsevier Ltd, Oxford, and previous editions of this series
    • For reviews on applications see: B. W. Fravel and N. A. Nedolya, in Comprehensive Heterocyclic Chemistry III, ed., A. R. Katritzky, C. A. Ramsden, E. F. V. Scriven, and, R. J. K. Taylor, Elsevier Ltd, Oxford, 2008, vol. 7, pp. 701-726 and previous editions of this series
    • (2008) Comprehensive Heterocyclic Chemistry III , pp. 701-726
    • Fravel, B.W.1    Nedolya, N.A.2
  • 21
    • 85034334867 scopus 로고    scopus 로고
    • and references cited therein For leading references on Au-catalyzed hydroarylation to form chromenes see:
    • S. Chang R. H. Grubbs J. Org. Chem. 1998 63 864
    • (1998) J. Org. Chem. , vol.63 , pp. 864
    • Chang, S.1    Grubbs, R.H.2
  • 38
    • 70349119910 scopus 로고    scopus 로고
    • As suggested by a reviewer, the reaction was also run with the conditions in Table 1, entry 8 and in the presence of 1 equivalent of p-nitrophenol. After 20 h, only 50% conversion was achieved and 6 was isolated in 32% yield
    • P. Kothandaraman S. J. Foo P. W. H. Chan J. Org. Chem. 2009 74 5947
    • (2009) J. Org. Chem. , vol.74 , pp. 5947
    • Kothandaraman, P.1    Foo, S.J.2    Chan, P.W.H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.