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Volumn 29, Issue 2, 1996, Pages 31-39

Nonnatural products nonpariel

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Indexed keywords


EID: 0038877775     PISSN: 00025100     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (6)

References (88)
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  • 9
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    • Hudson, R. A., communication to W. Wulff, 1996
    • Hudson, R. A., communication to W. Wulff, 1996.
  • 10
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    • Beckman Center for the History of Chemistry: Philadelphia
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  • 16
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  • 17
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    • John Wiley: New York
    • (b) The triangular symbols for the four terrestrial elements were apparently first employed by alchemists in the 13th century. Wentrup, C. Reactive Molecules; John Wiley: New York, 1984; p xi. No corresponding symbol was assigned to the celestial element. However, since both ancient and medieval philosophers viewed the circle as exemplifying the qualities of harmony, order, and perfection, which they also attributed to the heavenly spheres, its use here would seem appropriate.
    • (1984) Reactive Molecules
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    • Photo courtesy of William Bunnelle
    • Photo courtesy of William Bunnelle.
  • 23
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    • Millikan, R., communication to W. Wulff, 1996
    • Millikan, R., communication to W. Wulff, 1996.
  • 28
    • 0003882452 scopus 로고
    • Columbia University Press: New York
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    • (a) Transition-metal-catalyzed rearrangments: Eaton, P.E.; Patterson, D.R. J. Am. Chem. Soc. 1978, 100, 2573. Eaton, P.E.; Cassar, L.; Hudson, R.A.; Hwang, D.R. J. Org. Chem. 1976, 41, 1445. Cassar, L.; Eaton, P.E.; Halpern, J. J. Am. Chem. Soc. 1970, 92, 6366. Idem ibid. 1970, 92, 3515.
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    • Eaton, P.E.1    Patterson, D.R.2
  • 43
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    • (a) Transition-metal-catalyzed rearrangments: Eaton, P.E.; Patterson, D.R. J. Am. Chem. Soc. 1978, 100, 2573. Eaton, P.E.; Cassar, L.; Hudson, R.A.; Hwang, D.R. J. Org. Chem. 1976, 41, 1445. Cassar, L.; Eaton, P.E.; Halpern, J. J. Am. Chem. Soc. 1970, 92, 6366. Idem ibid. 1970, 92, 3515.
    • (1976) J. Org. Chem. , vol.41 , pp. 1445
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  • 44
    • 0000661089 scopus 로고
    • (a) Transition-metal-catalyzed rearrangments: Eaton, P.E.; Patterson, D.R. J. Am. Chem. Soc. 1978, 100, 2573. Eaton, P.E.; Cassar, L.; Hudson, R.A.; Hwang, D.R. J. Org. Chem. 1976, 41, 1445. Cassar, L.; Eaton, P.E.; Halpern, J. J. Am. Chem. Soc. 1970, 92, 6366. Idem ibid. 1970, 92, 3515.
    • (1970) J. Am. Chem. Soc. , vol.92 , pp. 6366
    • Cassar, L.1    Eaton, P.E.2    Halpern, J.3
  • 45
    • 33746311385 scopus 로고
    • (a) Transition-metal-catalyzed rearrangments: Eaton, P.E.; Patterson, D.R. J. Am. Chem. Soc. 1978, 100, 2573. Eaton, P.E.; Cassar, L.; Hudson, R.A.; Hwang, D.R. J. Org. Chem. 1976, 41, 1445. Cassar, L.; Eaton, P.E.; Halpern, J. J. Am. Chem. Soc. 1970, 92, 6366. Idem ibid. 1970, 92, 3515.
    • (1970) J. Am. Chem. Soc. , vol.92 , pp. 3515
    • Cassar, L.1    Eaton, P.E.2    Halpern, J.3
  • 47
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    • Rearrangement of cubyl azide: Eaton, P.E.; Hormann, R.E. ibid. 1987, 109, 1268. Eaton, P.E.; Fisher, A.M.; Hormann, R.E. Synlett 1990, 12, 737.
    • (1987) J. Am. Chem. Soc. , vol.109 , pp. 1268
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  • 48
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    • (c) Rearrangement of cubyl azide: Eaton, P.E.; Hormann, R.E. ibid. 1987, 109, 1268. Eaton, P.E.; Fisher, A.M.; Hormann, R.E. Synlett 1990, 12, 737.
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    • Paris
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    • Berthelot, M. Chimie Organique Fondee sur la Synthese, Paris, 1860; quoted in Leicester, H.M.; Klickstein, H.S. A Source Book in Chemistry 1400-1900; McGraw-Hill: New York, 1952; (reprinted, Harvard University Press: Cambridge, 1965) p 430; quoted in Fleming, I. Selected Organic Syntheses; John Wiley: London, 1973; p 8.
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    • Berthelot, M. Chimie Organique Fondee sur la Synthese, Paris, 1860; quoted in Leicester, H.M.; Klickstein, H.S. A Source Book in Chemistry 1400-1900; McGraw-Hill: New York, 1952; (reprinted, Harvard University Press: Cambridge, 1965) p 430; quoted in Fleming, I. Selected Organic Syntheses; John Wiley: London, 1973; p 8.
    • (1973) Selected Organic Syntheses , pp. 8
    • Fleming, I.1


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