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Volumn , Issue 9, 2006, Pages 1446-1448

An efficient access to 4-alkylidene-5,6-dihydro-4H-pyrrolo[1,2-c][1,2,3] triazoles

Author keywords

1,2,3 trizaole; 1,3 dipolar cycloaddition; Alkylidenecyclopropanes (MCPs); Heck reaction

Indexed keywords

4 ALKYLIDENE 5,6 DIHYDRO 4H PYRROLO[1,2 C]TRIAZOLE DERIVATIVE; ALKYLIDENECYCLOPROPANE DERIVATIVE; CYCLOPROPANE DERIVATIVE; TRIAZOLE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 33745378035     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-939708     Document Type: Article
Times cited : (26)

References (42)
  • 18
    • 0001487604 scopus 로고    scopus 로고
    • (f) For synthesis of MCPs, see: Brandi, A.; Goti, A. Chem. Rev. 1998, 98, 589.
    • (1998) Chem. Rev. , vol.98 , pp. 589
    • Brandi, A.1    Goti, A.2
  • 34
    • 33745333800 scopus 로고    scopus 로고
    • note
    • The temperature (70 °C) is required for the triazole synthesis step in our reaction by trial and error. At higher temperature 1,5-regioisomers can be formed and at lower temperature the reaction was not complete after several hours.
  • 42
    • 0000407644 scopus 로고    scopus 로고
    • (h) For a recent mechanistic study on Heck-type reaction see: Amatorc, C.; Jutand, A. J. Organomet. Chem. 1999, 576, 254.
    • (1999) J. Organomet. Chem. , vol.576 , pp. 254


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.