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Volumn 57, Issue 5, 2001, Pages 899-905

Ab initio study of Lewis acid catalyzed nitrone cycloaddition to electron deficient alkenes. Does a Lewis acid catalyst change the reaction mechanism?

Author keywords

Ab initio calculation; Lewis acid catalyst; Michael reaction; Nitrone; Reaction mechanism; Transition state

Indexed keywords

ACID; ACROLEIN; ALKENE; CARBONYL DERIVATIVE; NITROGEN DERIVATIVE;

EID: 0035961106     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(00)01045-0     Document Type: Article
Times cited : (65)

References (39)
  • 1
    • 84886996584 scopus 로고
    • 1,3-Dipolar Cycloaddition Chemistry, Wiley-Interscience: New York
    • (1984) , vol.1-2
    • Padwa, A.1
  • 15
    • 0002490493 scopus 로고
    • 1,3-Dipolar cycloaddition. Introduction, survey, mechanics
    • 1,3-Dipolar Cycloaddition Chemistry, Padwa, A., Ed. Wiley-Interscience: New York
    • (1984) , vol.1 , pp. 1-176
    • Huisgen, R.1
  • 36
    • 0006376088 scopus 로고    scopus 로고
    • note
  • 37
    • 0002108906 scopus 로고
    • Nitrones
    • 1,3-Dipolar Cycloaddition Chemistry, Padwa, A., Ed., Wiley-Interscience: New York
    • (1984) , vol.2 , pp. 83-168
    • Tufariello, J.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.