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Volumn 12, Issue 10, 2010, Pages 2234-2237

Synthesis of 2H-indazoles by the [3 + 2] cycloaddition of arynes and sydnones

Author keywords

[No Author keywords available]

Indexed keywords

ALKYNE; INDAZOLE DERIVATIVE; SYDNONE DERIVATIVE;

EID: 77952386310     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol100586r     Document Type: Article
Times cited : (156)

References (68)
  • 1
    • 77952342288 scopus 로고    scopus 로고
    • For excellent reviews of indazoles activity and synthesis, see
    • For excellent reviews of indazoles activity and synthesis, see
  • 3
    • 0038607286 scopus 로고    scopus 로고
    • Georg Thieme; Stuttgart
    • Stadlbauer, W. In Science of Synthesis; Georg Thieme; Stuttgart, 2002; Vol. 12, pp 227 - 324.
    • (2002) Science of Synthesis , vol.12 , pp. 227-324
    • Stadlbauer, W.1
  • 11
    • 77952327502 scopus 로고    scopus 로고
    • For one successful example, see
    • For one successful example, see
  • 19
    • 77952373174 scopus 로고    scopus 로고
    • For comprehensive reviews of 1,3-dipolar cycloadditions, see
    • For comprehensive reviews of 1,3-dipolar cycloadditions, see
  • 22
    • 77952382186 scopus 로고    scopus 로고
    • For our recent work in aryne 1,3-dipolar cycloadditions, see
    • For our recent work in aryne 1,3-dipolar cycloadditions, see
  • 28
    • 77952374700 scopus 로고    scopus 로고
    • For others work in aryne 1,3-dipolar cycloadditions, see
    • For others work in aryne 1,3-dipolar cycloadditions, see
  • 40
    • 77952379185 scopus 로고    scopus 로고
    • For reviews on sydnones, see
    • For reviews on sydnones, see
  • 48
    • 77952332238 scopus 로고    scopus 로고
    • For selected examples, see
    • For selected examples, see
  • 58
    • 77952331758 scopus 로고    scopus 로고
    • There is a significant side product in this reaction, whose identity is currently under investigation. The results will be published in due course
    • There is a significant side product in this reaction, whose identity is currently under investigation. The results will be published in due course.
  • 59
    • 77952357228 scopus 로고    scopus 로고
    • For a recent investigation of these biased substituted arynes, see
    • For a recent investigation of these biased substituted arynes, see
  • 65
    • 77952412065 scopus 로고    scopus 로고
    • We are currently investigating other substrates in this class, and the results will also be published in due course. Currently, we tend to believe that these substrates may be unstable under the reaction conditions
    • We are currently investigating other substrates in this class, and the results will also be published in due course. Currently, we tend to believe that these substrates may be unstable under the reaction conditions.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.