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Volumn 630, Issue 1, 2001, Pages 118-124

Behaviour of monocomplexed 1,4-diynes in the Khand reaction and use of ethylene equivalent techniques in a convenient route to tritium-labelled methyl jasmonate

Author keywords

Ethylene equivalent; Khand reaction; Methyl dehydrojasmonate; Methyl jasmonate; Tritium; Vinyl esters

Indexed keywords

TRITIUM;

EID: 0009021719     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-328X(01)00890-7     Document Type: Article
Times cited : (20)

References (30)
  • 4
    • 0039926472 scopus 로고    scopus 로고
    • Dr M.H. Zenk (zenk@lrz.uni-muenchen.de), Dr M.J. Müller (martin.mueller@lrz.uni-muenchen.de), Pharmazeutische Biologie, Universität München, Karlstrasse 29, 80333 München, Germany, fax: +49-89-590-2611.
    • Dr M.H. Zenk (zenk@lrz.uni-muenchen.de), Dr M.J. Müller (martin.mueller@lrz.uni-muenchen.de), Pharmazeutische Biologie, Universität München, Karlstrasse 29, 80333 München, Germany, fax: +49-89-590-2611.
  • 5
    • 0039334153 scopus 로고    scopus 로고
    • Dr E.W. Weiler, Lehrstuhl für Planzenphysiologie, Fakultät für Biologie, Ruhr-Universität Bochum, Gebäude ND 3/30, Posfach 10 21 48, Universitätsstrasse, 150, D-44801 Bochum, Germany, Tel.: +49-2-34-700-4291; fax: +49-2-34-709-4187.
    • Dr E.W. Weiler, Lehrstuhl für Planzenphysiologie, Fakultät für Biologie, Ruhr-Universität Bochum, Gebäude ND 3/30, Posfach 10 21 48, Universitätsstrasse, 150, D-44801 Bochum, Germany, Tel.: +49-2-34-700-4291; fax: +49-2-34-709-4187.
  • 9
    • 0041113422 scopus 로고    scopus 로고
    • We are grateful to Dr R. Colman of Lancaster Synthesis Ltd, Newgate, White Lund, Morcambe, Lancashire, LA3 3DY, UK, for supplying us with this reagent.
    • We are grateful to Dr R. Colman of Lancaster Synthesis Ltd, Newgate, White Lund, Morcambe, Lancashire, LA3 3DY, UK, for supplying us with this reagent.
  • 10
    • 0039334154 scopus 로고    scopus 로고
    • Surprisingly, the use of vinyl acetate, in place of the benzoate, with complex 4a afforded the unreduced cyclopentenone, 5-acetoxy-2-(pent-2-yn-1-yl)cyclopent-2-en-1-one (13% yield), as the main isolable product; see Section 4.
    • Surprisingly, the use of vinyl acetate, in place of the benzoate, with complex 4a afforded the unreduced cyclopentenone, 5-acetoxy-2-(pent-2-yn-1-yl)cyclopent-2-en-1-one (13% yield), as the main isolable product; see Section 4.
  • 18
    • 0041113379 scopus 로고    scopus 로고
    • The radiolabelling step was performed in the laboratory of Professor J.R. Jones, Department of Chemistry, University of Surrey, Guilford, Surrey, GU2 7XH, UK, Tel.: +44-1483-259313, e-mail: j.r.jones@surrey.ac.uk. We thank Professor Jones and his co-workers for their assistance.
    • The radiolabelling step was performed in the laboratory of Professor J.R. Jones, Department of Chemistry, University of Surrey, Guilford, Surrey, GU2 7XH, UK, Tel.: +44-1483-259313, e-mail: j.r.jones@surrey.ac.uk. We thank Professor Jones and his co-workers for their assistance.
  • 29
    • 0041113378 scopus 로고    scopus 로고
    • Commercial sample obtained from Firmenich Chemical Co., Switzerland.
    • Commercial sample obtained from Firmenich Chemical Co., Switzerland.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.