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Volumn 28, Issue 52, 1987, Pages 6553-6556

Studies on tandem ene/intramolecular diels-alder reactions

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0000439008     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)96911-9     Document Type: Article
Times cited : (89)

References (16)
  • 8
    • 84919125197 scopus 로고    scopus 로고
    • a, Spectroscopic data obtained for all new compounds were fully consistent with the assigned structures. b) Thermal reactions were typically run using one mmol of enophile and at high power setting in sealed tubes. The reaction of 1 to give 4 has been scaled up under microwave conditions (6 minutes) to one gram in 75% yield. c) New compound(s).
  • 13
    • 84919125196 scopus 로고    scopus 로고
    • 3 in sealed tubes with an ene:enophile ratio of 15:1.
  • 15
    • 84919125195 scopus 로고    scopus 로고
    • No direct or indirect evidence has been obtained for this conjecture.
  • 16
    • 33646525045 scopus 로고
    • Methyl methacrylate reacts with 9,10-dimethylanthracene thirty times faster at +20°C than methyl trans-crotonate, an isomeric dienophile, cf.
    • (1965) Z. Naturforsch. , vol.206 , pp. 637
    • Schenck1    Kopp2    Kim3    Koerner4    Gastorf5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.