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Volumn 351, Issue 18, 2009, Pages 3083-3088

Alkynyl group as activating group: Base-catalyzed diastereoselective domino reactions of electron-deficient enynes

Author keywords

Alkynes; Cyclohexanes; Cyclopentanes; Domino reactions; Michael reaction; Stereoselectivity

Indexed keywords


EID: 73349113496     PISSN: 16154150     EISSN: 15213897     Source Type: Journal    
DOI: 10.1002/adsc.200900633     Document Type: Article
Times cited : (24)

References (56)
  • 1
    • 73349131314 scopus 로고    scopus 로고
    • For recent reviews of domino reactions, please see
    • For recent reviews of domino reactions, please see:
  • 5
    • 33845458327 scopus 로고    scopus 로고
    • T. J. J. Müller, in: Topics in Organometallic Chemistry, (Ed.: T. J. J. Müller), Springer Verlag, Berlin, 2006, 19, p 149; e) Domino Reactions in Organic Synthesis, (Eds.: L. F. Tietze, G. Brasche, K. M. Gericke), Wiley-VCH, Weinheim, 2006, p359;
    • T. J. J. Müller, in: Topics in Organometallic Chemistry, (Ed.: T. J. J. Müller), Springer Verlag, Berlin, 2006, Vol. 19, p 149; e) Domino Reactions in Organic Synthesis, (Eds.: L. F. Tietze, G. Brasche, K. M. Gericke), Wiley-VCH, Weinheim, 2006, p359;
  • 14
    • 73349138778 scopus 로고    scopus 로고
    • For reviews of double Michael addition reactions, please see
    • For reviews of double Michael addition reactions, please see:
  • 17
    • 0035136830 scopus 로고    scopus 로고
    • For leading examples of tandem double Michael additions, please see
    • R. B. Grossman, Synlett., 2001, 13. For leading examples of tandem double Michael additions, please see:
    • (2001) Synlett , pp. 13
    • Grossman, R.B.1
  • 20
    • 73349113723 scopus 로고    scopus 로고
    • Z. Lu G. Chai S. Ma Angew. Chem. 2008 120 6134; Angew. Chem. Int. Ed. 2008 47 6045 ;
    • Z. Lu G. Chai S. Ma Angew. Chem. 2008 120 6134; Angew. Chem. Int. Ed. 2008 47 6045 ;
  • 27
    • 53849109140 scopus 로고    scopus 로고
    • For the work from our group in which the alkynyl group is reacting group please see: a
    • For the work from our group in which the alkynyl group is reacting group please see: a) Y. Xiao J. Zhang Angew. Chem. 2008 120 1929;
    • (2008) Angew. Chem , vol.120 , pp. 1929
    • Xiao, Y.1    Zhang, J.2
  • 34
    • 73349114200 scopus 로고    scopus 로고
    • For work from other groups in which the alkynyl group is also reacting group, please see
    • For work from other groups in which the alkynyl group is also reacting group, please see:
  • 39
    • 73349090470 scopus 로고    scopus 로고
    • For reviews of the synthesis and bioactivities of cyclopentanes, please see
    • For reviews of the synthesis and bioactivities of cyclopentanes, please see:
  • 47
    • 73349140092 scopus 로고    scopus 로고
    • CCDC 742299 (3a), CCDC 742298 (4a), CCDC 742300 (the minor diastereomer of 10a), and CCDC 747498 (12) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
    • CCDC 742299 (3a), CCDC 742298 (4a), CCDC 742300 (the minor diastereomer of 10a), and CCDC 747498 (12) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
  • 48
    • 73349089833 scopus 로고    scopus 로고
    • An Au (I)-catalyzed selective conversion of compounds 4 into cyclohexenes or 5, 6-fused bicyclic compounds has been developed and these results will be reported in due course.
    • An Au (I)-catalyzed selective conversion of compounds 4 into cyclohexenes or 5, 6-fused bicyclic compounds has been developed and these results will be reported in due course.
  • 49
    • 73349088618 scopus 로고    scopus 로고
    • Alkyne-ketone metathesis, please see
    • Alkyne-ketone metathesis, please see:


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.