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Volumn , Issue 10, 1998, Pages 2243-2247

Pentazole chemistry: The mechanism of the reaction of aryldiazonium chlorides with azide ion at -80 °C: Concerted versus stepwise formation of arylpentazoles, detection of a pentazene intermediate, a combined 1H and 15N NMR experimental and ab initio theoretical study

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EID: 0002815581     PISSN: 03009580     EISSN: None     Source Type: Journal    
DOI: 10.1039/a804040k     Document Type: Article
Times cited : (52)

References (24)
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    • Series eds. A. R. Katritzky, C. W. Rees, Pergamon Press, Oxford
    • For reviews see, (a) I. Ugi, Comprehensive Heterocyclic Chemistry, Series eds. A. R. Katritzky, C. W. Rees, Pergamon Press, Oxford, 1984, vol. 5, p. 839; (b) R. N. Butler, Comprehensive Heterocyclic Chemistry 11, Series eds., A. R. Katritzky, C. W. Rees, E. F. V. Scriven, Pergamon Press, Oxford, 1996, vol. 4, (ed., R. C. Storr), p. 897.
    • (1984) Comprehensive Heterocyclic Chemistry , vol.5 , pp. 839
    • Ugi, I.1
  • 2
    • 79952751142 scopus 로고    scopus 로고
    • Series eds., A. R. Katritzky, C. W. Rees, E. F. V. Scriven, Pergamon Press, Oxford, ed., R. C. Storr
    • For reviews see, (a) I. Ugi, Comprehensive Heterocyclic Chemistry, Series eds. A. R. Katritzky, C. W. Rees, Pergamon Press, Oxford, 1984, vol. 5, p. 839; (b) R. N. Butler, Comprehensive Heterocyclic Chemistry 11, Series eds., A. R. Katritzky, C. W. Rees, E. F. V. Scriven, Pergamon Press, Oxford, 1996, vol. 4, (ed., R. C. Storr), p. 897.
    • (1996) Comprehensive Heterocyclic Chemistry 11 , vol.4 , pp. 897
    • Butler, R.N.1
  • 8
    • 0000169641 scopus 로고
    • and references therein
    • For a review see A. F. Hegarty, Acc. Chem. Res., 1980, 13, 448 and references therein.
    • (1980) Acc. Chem. Res. , vol.13 , pp. 448
    • Hegarty, A.F.1
  • 10
    • 0347813668 scopus 로고
    • A. F. Hegarty and M. T. McCormack, J. Chem. Soc., Perkin Trans. 2, 1976, 1701; J. Chem. Soc., Chem. Commun., 1975, 168.
    • (1975) J. Chem. Soc., Chem. Commun. , pp. 168
  • 13
  • 15
    • 0011392312 scopus 로고
    • M. F. Ahearn, A. Leopold, J. R. Bradle and G. W. Gokel, J. Am. Chem. Soc., 1982, 104, 548; R. M. Elofson, N. Cry, J. K. Laidler and K. F. Schulz, Tetrahedron Lett., 1984, 3039; E. S. Lewis and H. Suhr, Chem. Ber., 1959, 92, 3043.
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 548
    • Ahearn, M.F.1    Leopold, A.2    Bradle, J.R.3    Gokel, G.W.4
  • 16
    • 0000156880 scopus 로고
    • M. F. Ahearn, A. Leopold, J. R. Bradle and G. W. Gokel, J. Am. Chem. Soc., 1982, 104, 548; R. M. Elofson, N. Cry, J. K. Laidler and K. F. Schulz, Tetrahedron Lett., 1984, 3039; E. S. Lewis and H. Suhr, Chem. Ber., 1959, 92, 3043.
    • (1984) Tetrahedron Lett. , pp. 3039
    • Elofson, R.M.1    Cry, N.2    Laidler, J.K.3    Schulz, K.F.4
  • 17
    • 0347183611 scopus 로고
    • M. F. Ahearn, A. Leopold, J. R. Bradle and G. W. Gokel, J. Am. Chem. Soc., 1982, 104, 548; R. M. Elofson, N. Cry, J. K. Laidler and K. F. Schulz, Tetrahedron Lett., 1984, 3039; E. S. Lewis and H. Suhr, Chem. Ber., 1959, 92, 3043.
    • (1959) Chem. Ber. , vol.92 , pp. 3043
    • Lewis, E.S.1    Suhr, H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.