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Volumn , Issue 7, 2003, Pages 1018-1024

Triphenylphosphine catalyzed Michael addition of oximes onto activated olefins

Author keywords

Alkenes; Catalysis; Michael additions; Oximes; Phosphorus

Indexed keywords

ACRYLICS; CATALYSIS; KETONES;

EID: 0037680780     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2003-39162     Document Type: Article
Times cited : (43)

References (19)
  • 1
    • 0038359011 scopus 로고    scopus 로고
    • DRL Publication No. 284
    • DRL Publication No. 284.
  • 2
    • 0038359012 scopus 로고
    • Trost, B. M.; Flemming, I., Eds.; Pergamon: Oxford; and references therein
    • Jung, M. E. In Comprehensive Organic Synthesis, Vol. 4; Trost, B. M.; Flemming, I., Eds.; Pergamon: Oxford, 1991, 30-39; and references therein.
    • (1991) Comprehensive Organic Synthesis , vol.4 , pp. 30-39
    • Jung, M.E.1
  • 15
    • 0025305393 scopus 로고
    • and references cited herein (for anti-inflammatory study). In this report, twenty different aldoximes and ketoximes were added to ethyl acrylate using KOH (16 mol%) as base catalyst in EtOH solvent
    • As an example, see: Macchia, B.; Balsamo, A.; Lapucci, A.; Macchia, F.; Martinelli, A.; Nencetti, S.; Orlandini, E.; Baldacci, M.; Mengozzi, G.; Soldani, G.; Domiano, P. J. Med. Chem. 1990, 33, 1423; and references cited herein (for anti-inflammatory study). In this report, twenty different aldoximes and ketoximes were added to ethyl acrylate using KOH (16 mol%) as base catalyst in EtOH solvent.
    • (1990) J. Med. Chem. , vol.33 , pp. 1423
    • Macchia, B.1    Balsamo, A.2    Lapucci, A.3    Macchia, F.4    Martinelli, A.5    Nencetti, S.6    Orlandini, E.7    Baldacci, M.8    Mengozzi, G.9    Soldani, G.10    Domiano, P.11
  • 17
    • 0029796652 scopus 로고    scopus 로고
    • and references cited therein
    • Triphenylphosphine is known as a catalyst for the Michael addition of carbon nucleophiles. Please see: Gómez-Bengoa, E.; Cuerva, J. M.; Mateo, C.; Echavarren, A. M. J. Am. Chem. Soc. 1996, 118, 8553; and references cited therein.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 8553
    • Gómez-Bengoa, E.1    Cuerva, J.M.2    Mateo, C.3    Echavarren, A.M.4
  • 19
    • 0038697216 scopus 로고    scopus 로고
    • note
    • Oximes were prepared by reacting the corresponding carbonyl compounds with excess of hydroxylamine in methanol, either at r.t. or when required under heating (55°c).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.