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Volumn 10, Issue 5, 2008, Pages 689-692

Cycloadditions of aromatic azomethine imines with 1,1-cyclopropane Diesters

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EID: 46949106418     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol702414e     Document Type: Article
Times cited : (193)

References (51)
  • 1
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    • Selected examples: (a) Daly, J. W.; Spande, T. F.; Garraffo, H. M. J. Nat. Prod. 2005, 68, 1556.
    • Selected examples: (a) Daly, J. W.; Spande, T. F.; Garraffo, H. M. J. Nat. Prod. 2005, 68, 1556.
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    • Selected examples: (a) Yamaoka, Y.; Miyabe, H.; Takemoto, Y. J. Am. Chem. Soc. 2007, 129, 6686.
    • Selected examples: (a) Yamaoka, Y.; Miyabe, H.; Takemoto, Y. J. Am. Chem. Soc. 2007, 129, 6686.
  • 13
    • 9744249469 scopus 로고    scopus 로고
    • For excellent reviews on the chemistry of donor-acceptor and electrophilic cyclopropanes, see: a
    • For excellent reviews on the chemistry of donor-acceptor and electrophilic cyclopropanes, see: (a) Yu, M.; Pagenkopf, B. L. Tetrahedron 2005, 61, 321.
    • (2005) Tetrahedron , vol.61 , pp. 321
    • Yu, M.1    Pagenkopf, B.L.2
  • 15
    • 15644378136 scopus 로고    scopus 로고
    • Wong, H. N. C.; Hon, M.-Y.; Tse, C.-W.; Yip, Y.-C; Tanko, J.; Hudlicky, T. Chem. Rev. 1989, 89, 165. (d) Danishefsky, S. Acc. Chem. Res. 1979, 12, 66.
    • (c) Wong, H. N. C.; Hon, M.-Y.; Tse, C.-W.; Yip, Y.-C; Tanko, J.; Hudlicky, T. Chem. Rev. 1989, 89, 165. (d) Danishefsky, S. Acc. Chem. Res. 1979, 12, 66.
  • 47
    • 58149189175 scopus 로고    scopus 로고
    • Reaction was carried out in the absence of 3 Å molecular sieves to give 45% conversion. Addition of water (30 equiv) in the reaction also inhibited the formation of the desired product, giving 7% yield.
    • Reaction was carried out in the absence of 3 Å molecular sieves to give 45% conversion. Addition of water (30 equiv) in the reaction also inhibited the formation of the desired product, giving 7% yield.
  • 48
    • 58149184444 scopus 로고    scopus 로고
    • 58% yield was obtained using 10 equiv of the commercially available cyclopropane.
    • 58% yield was obtained using 10 equiv of the commercially available cyclopropane.
  • 50
    • 58149189176 scopus 로고    scopus 로고
    • For a proposed mechanism of cycloaddition reactions, see refs 7a and 16
    • For a proposed mechanism of cycloaddition reactions, see refs 7a and 16.
  • 51
    • 58149196919 scopus 로고    scopus 로고
    • See the Supporting Information for details
    • See the Supporting Information for details.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.