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Volumn 51, Issue 2, 2010, Pages 411-414

Cycloaddition of trifluoromethyl azafulvenium methides: synthesis of new trifluoromethylpyrrole-annulated derivatives

Author keywords

1,3 Dipolar cycloaddition; 1,3 Dipoles; 1,7 Dipoles; 1,7 Electrocyclization; 8 +2 Cycloaddition; Azafulvenium methides; Azomethine ylides; Microwave; Trifluoromethylpyrroles

Indexed keywords

PYRROLE DERIVATIVE; TRIFLUOROMETHYL AZAFULVENIUM METHIDE; TRIFLUOROMETHYLPYRROLE; UNCLASSIFIED DRUG;

EID: 71049167666     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.11.033     Document Type: Article
Times cited : (22)

References (35)
  • 1
    • 0001426611 scopus 로고    scopus 로고
    • For reviews on pyrrole, see:. Katritzky A.R., Rees C.W., and Scriven E.F.V. (Eds), Pergamon, Oxford
    • For reviews on pyrrole, see:. Sundberg R.J. In: Katritzky A.R., Rees C.W., and Scriven E.F.V. (Eds). Comprehensive Heterocyclic Chemistry Vol. 2 (1996), Pergamon, Oxford 119-206
    • (1996) Comprehensive Heterocyclic Chemistry , vol.2 , pp. 119-206
    • Sundberg, R.J.1
  • 34
    • 0035953032 scopus 로고    scopus 로고
    • Using the general synthetic procedure described in:
    • Using the general synthetic procedure described in:. Sato K., Hyodo M., Aoki M., Zheng X.-Q., and Noyori R. Tetrahedron 57 (2001) 2469-2476
    • (2001) Tetrahedron , vol.57 , pp. 2469-2476
    • Sato, K.1    Hyodo, M.2    Aoki, M.3    Zheng, X.-Q.4    Noyori, R.5
  • 35
    • 71049119294 scopus 로고    scopus 로고
    • note
    • 1H NMR spectrum (see Supplementary data).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.