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Volumn , Issue 15, 2006, Pages 3451-3456

New metal-catalyzed synthesis of quinoline and chromene skeletons

Author keywords

Chromene; Conjugate elimination; Conjugated dienes; Quinoline; Suzuki cross coupling

Indexed keywords


EID: 33746577404     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200600230     Document Type: Article
Times cited : (16)

References (55)
  • 1
    • 0000578235 scopus 로고
    • Eds.: G. Wilkinson, F. G. A. Stone, Pergamon Press, Oxford, and references cited therein
    • J. P. Collman, B. M. Trost, T. R. Verhoeven, in Comprehensive Organometallic Chemistry (Eds.: G. Wilkinson, F. G. A. Stone), Pergamon Press, Oxford, 1982, vol. 8, p. 892; and references cited therein.
    • (1982) Comprehensive Organometallic Chemistry , vol.8 , pp. 892
    • Collman, J.P.1    Trost, B.M.2    Verhoeven, T.R.3
  • 3
    • 0347612039 scopus 로고
    • Eds.: A. J. Boulton, A. McKillop, Pergamon Press, New York, chapter 2.09
    • F. S. Yates, in Comprehensive Heterocyclic Chemistry (Eds.: A. J. Boulton, A. McKillop), Pergamon Press, New York, 1984, vol. 2, chapter 2.09.
    • (1984) Comprehensive Heterocyclic Chemistry , vol.2
    • Yates, F.S.1
  • 32
    • 0001834816 scopus 로고
    • Ed.: V. Snieckus, JAI Press, Inc., Greenwich, CT
    • c) A. Mordini, in Advances in Carbanion Chemistry (Ed.: V. Snieckus), JAI Press, Inc., Greenwich, CT, 1992, vol. 1, pp. 1-45;
    • (1992) Advances in Carbanion Chemistry , vol.1 , pp. 1-45
    • Mordini, A.1
  • 45
    • 33746543551 scopus 로고    scopus 로고
    • note
    • In the case of cross-coupling derivative 3d both (E) and (Z) isomers have been characterized, and the stereochemistry has been deduced on the basis of NOESY experiments (see Experimental Section).
  • 46
    • 33746481552 scopus 로고    scopus 로고
    • note
    • II, has also to be considered. At this moment we have no explanation for the results regarding cross-coupling product 3c and 3f.
  • 48
    • 33746516698 scopus 로고    scopus 로고
    • note
    • 3 can be likely considered a weak proton scavenger.
  • 53
    • 33746572660 scopus 로고    scopus 로고
    • note
    • The reaction reported in Scheme 6 has also been carried out using 3a in the presence of 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ), and no significant increase in reaction rate and yield has been observed.
  • 55
    • 33746534798 scopus 로고    scopus 로고
    • [18b]
    • [18b]


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.