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Volumn 13, Issue 5, 2011, Pages 1138-1141

Unusual formal [4 + 2] cycloaddition of ethyl allenoate with arylidenoxindoles: Synthesis of dihydropyran-fused indoles

Author keywords

[No Author keywords available]

Indexed keywords

INDOLE DERIVATIVE; PYRAN DERIVATIVE;

EID: 79952168191     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol103165y     Document Type: Article
Times cited : (60)

References (101)
  • 59
    • 26444543230 scopus 로고    scopus 로고
    • Annulation reactions that utilize the two-carbon reactivity of allenoates with other substrates; see
    • Annulation reactions that utilize the two-carbon reactivity of allenoates with other substrates; see: Zhao, G.-L.; Shi, Y.-L.; Shi, M. Org. Lett. 2005, 7, 4527
    • (2005) Org. Lett. , vol.7 , pp. 4527
    • Zhao, G.-L.1    Shi, Y.-L.2    Shi, M.3
  • 65
    • 0141885412 scopus 로고    scopus 로고
    • The DABCO-catalyzed coupling of allenoates to enones has been reported
    • The DABCO-catalyzed coupling of allenoates to enones has been reported: Evans, C. A.; Miller, S. J. J. Am. Chem. Chem. 2003, 125, 12394
    • (2003) J. Am. Chem. Chem. , vol.125 , pp. 12394
    • Evans, C.A.1    Miller, S.J.2
  • 66
    • 2942609168 scopus 로고    scopus 로고
    • For reviews, see
    • For reviews, see: Zeni, G.; Larock, R. C. Chem. Rev. 2004, 104, 2285
    • (2004) Chem. Rev. , vol.104 , pp. 2285
    • Zeni, G.1    Larock, R.C.2
  • 89
    • 79952164780 scopus 로고    scopus 로고
    • 2O (74% yield), or DCM (65% yield), was not beneficial for this cycloaddition reaction.
    • 2O (74% yield), or DCM (65% yield), was not beneficial for this cycloaddition reaction.
  • 90
    • 79952169888 scopus 로고    scopus 로고
    • See Supporting Information for details.
    • See Supporting Information for details.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.