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Volumn 82, Issue 2, 2010, Pages 1029-1081

4-alkynoic acids in the synthesis of biologically important tetrapyrroles

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EID: 79952753355     PISSN: 03855414     EISSN: 18810942     Source Type: Journal    
DOI: 10.3987/REV-10-SR(E)6     Document Type: Review
Times cited : (18)

References (136)
  • 36
    • 0029826917 scopus 로고    scopus 로고
    • S. H. Bertz, M. Eriksson, G. Miao, and J. Snyder, J. Am. Chem. Soc, 1996, 118, 10906. The methyl transfer reagent was prepared following the procedure given for the corresponding n-butyl species.
    • (1996) J. Am. Chem. Soc , vol.118 , pp. 10906
    • Bertz, S.H.1    Eriksson, M.2    Miao, G.3    Snyder, J.4
  • 39
    • 0034609680 scopus 로고    scopus 로고
    • We gratefully acknowledge stimulating discussions with Professor Liebeskind on this subject
    • C. Savarin, J. Srogl, and L. S. Liebeskind, Org. Lett., 2000, 2, 3229; We gratefully acknowledge stimulating discussions with Professor Liebeskind on this subject;
    • (2000) Org. Lett. , vol.2 , pp. 3229
    • Savarin, C.1    Srogl, J.2    Liebeskind, L.S.3
  • 40
    • 79952742766 scopus 로고    scopus 로고
    • note
    • For best results the MeZnI reagent must be prepared following the procedure of Fukuyama et al. (Ref. 16a). The reagent derived by treatment of MeMgCl with ZnI was considerably less reactive.
  • 53
    • 33646268363 scopus 로고
    • R. A. Jones, Ed.; The Chemistry of Heterocyclic Compounds; John Wiley & Sons: New York
    • A. H. Jackson, in Pyrroles; R. A. Jones, Ed.; The Chemistry of Heterocyclic Compounds; John Wiley & Sons: New York, 1990; Vol. 48, Part 1. p 316.
    • (1990) Pyrroles , vol.48 , Issue.PART 1 , pp. 316
    • Jackson, A.H.1
  • 65
    • 33646265233 scopus 로고
    • R. L. Augustine, Ed., Marcel Dekker: New York
    • E. N. Trachtenberg, in Oxidation; R. L. Augustine, Ed.; Marcel Dekker: New York, 1969; p 19.
    • (1969) Oxidation , pp. 19
    • Trachtenberg, E.N.1
  • 80
    • 79952752267 scopus 로고    scopus 로고
    • Ph. D. thesis, Dartmouth College, Hanover, New Hampshire
    • W. G. O'Neal, Ph. D. thesis, Dartmouth College, Hanover, New Hampshire, 2007.
    • (2007)
    • O'Neal, W.G.1
  • 84
    • 79952757582 scopus 로고    scopus 로고
    • Ph. D. thesis, Wesleyan University, Middletown, Connecticut
    • H. Liu, Ph. D. thesis, Wesleyan University, Middletown, Connecticut, 1999.
    • (1999)
    • Liu, H.1
  • 90
    • 79952774333 scopus 로고    scopus 로고
    • We are grateful to Professor Doctor Albert Eschenmoser, ETH-Z, for providing us with experimental details and spectral data for several unpublished procedures
    • We are grateful to Professor Doctor Albert Eschenmoser, ETH-Z, for providing us with experimental details and spectral data for several unpublished procedures.
  • 91
    • 0344315948 scopus 로고
    • A. R. Katritzky and C. W. Rees, Ed., Pergamon Press Inc.: New York
    • A. R. Katritzky and J. M. Lagowski, in Comprehensive Heterocyclic Chemistry; A. R. Katritzky and C. W. Rees, Ed.; Pergamon Press Inc.: New York, 1984, Vol. 5, p 94.
    • (1984) Comprehensive Heterocyclic Chemistry , vol.5 , pp. 94
    • Katritzky, A.R.1    Lagowski, J.M.2
  • 92
    • 79952757186 scopus 로고    scopus 로고
    • We are grateful to Dr. Victor G. Young, X-ray Crystallographic Laboratory, Department of Chemistry, University of Minnesota, for carrying out this analysis
    • We are grateful to Dr. Victor G. Young, X-ray Crystallographic Laboratory, Department of Chemistry, University of Minnesota, for carrying out this analysis.
  • 93
    • 0028452890 scopus 로고
    • and references cited therein
    • A. R. Battersby, Science, 1994, 264, 1551, and references cited therein
    • (1994) Science , vol.264 , pp. 1551
    • Battersby, A.R.1
  • 97
    • 0017385449 scopus 로고
    • and references cited therein
    • A. Eschenmoser and C. E. Wintner, Science, 1977, 196, 1410, and references cited therein
    • (1977) Science , vol.196 , pp. 1410
    • Eschenmoser, A.1    Wintner, C.E.2
  • 136
    • 79952774138 scopus 로고    scopus 로고
    • The structure of the predominate (S)-relative epimer was confirmed by X-ray analysis of a racemic sample. We thank the University of Massachusetts Amherst X-ray Structural Characterization Facility (NSF CHE 9974648) for providing diffractometer access and Mr. Travis Benanti of that facility for data collection and refinement
    • The structure of the predominate (S)-relative epimer was confirmed by X-ray analysis of a racemic sample. We thank the University of Massachusetts Amherst X-ray Structural Characterization Facility (NSF CHE 9974648) for providing diffractometer access and Mr. Travis Benanti of that facility for data collection and refinement.


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