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Volumn 119, Issue 22, 1997, Pages 5091-5094

The chemistry of the N-methyl-3-dehydropyridinium ylid

Author keywords

[No Author keywords available]

Indexed keywords

PYRIDINIUM DERIVATIVE;

EID: 0030794629     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja9639168     Document Type: Article
Times cited : (22)

References (22)
  • 3
    • 1842315731 scopus 로고    scopus 로고
    • note
    • Although we have not yet carried out detailed calculations of the energy surfaces involved in these reactions, we note that geometry optimization at the MP2/6-31G* level demonstrates that planar 6a and 6b are energy minima. All attempts to find energy minima for cumulenes 7 gave 6 instead.
  • 4
    • 0001938664 scopus 로고
    • For reviews of the chemistry of atomic carbon, see: (a) Skell, P. S.; Havel J.; McGlinchey, M. J. Acc. Chem. Res. 1973, 6, 97. (b) MacKay, C. In Carbenes; Moss, R. A., Jones, M., Jr., Eds.; Wiley-Interscience: New York, 1975; Vol. II, pp 1-42. (c) Shevlin, P. B. In Reactive Intermediates; Abramovitch, R. A., Ed.; Plenum Press: New York, 1980; Vol. I, pp 1-36.
    • (1973) Acc. Chem. Res. , vol.6 , pp. 97
    • Skell, P.S.1    Havel, J.2    McGlinchey, M.J.3
  • 5
    • 0003128343 scopus 로고
    • Moss, R. A., Jones, M., Jr., Eds.; Wiley-Interscience: New York
    • For reviews of the chemistry of atomic carbon, see: (a) Skell, P. S.; Havel J.; McGlinchey, M. J. Acc. Chem. Res. 1973, 6, 97. (b) MacKay, C. In Carbenes; Moss, R. A., Jones, M., Jr., Eds.; Wiley-Interscience: New York, 1975; Vol. II, pp 1-42. (c) Shevlin, P. B. In Reactive Intermediates; Abramovitch, R. A., Ed.; Plenum Press: New York, 1980; Vol. I, pp 1-36.
    • (1975) Carbenes , vol.2 , pp. 1-42
    • MacKay, C.1
  • 6
    • 0002627789 scopus 로고
    • Abramovitch, R. A., Ed.; Plenum Press: New York
    • For reviews of the chemistry of atomic carbon, see: (a) Skell, P. S.; Havel J.; McGlinchey, M. J. Acc. Chem. Res. 1973, 6, 97. (b) MacKay, C. In Carbenes; Moss, R. A., Jones, M., Jr., Eds.; Wiley-Interscience: New York, 1975; Vol. II, pp 1-42. (c) Shevlin, P. B. In Reactive Intermediates; Abramovitch, R. A., Ed.; Plenum Press: New York, 1980; Vol. I, pp 1-36.
    • (1980) Reactive Intermediates , vol.1 , pp. 1-36
    • Shevlin, P.B.1
  • 8
    • 33845183891 scopus 로고
    • For a discussion of the various electronic states possible in cyclic cumulenes see ref 1.
    • (1989) Chem. Rev. , vol.89 , pp. 1111
    • Johnson, R.A.1
  • 11
    • 1842305295 scopus 로고    scopus 로고
    • Ph. D. Thesis, Auburn University
    • (c) LaFrancois, C., J. Ph. D. Thesis, Auburn University, 1996.
    • (1996)
    • LaFrancois, C.J.1
  • 12
    • 1842309089 scopus 로고
    • Ph. D. Thesis, Auburn University
    • (d) Sztyrbicka, R. Ph. D. Thesis, Auburn University, 1992.
    • (1992)
    • Sztyrbicka, R.1
  • 16
  • 22
    • 0003038406 scopus 로고
    • The deuterated N-methylpyrroles were prepared using the procedure for the unlabeled compound: Santaniello, E.; Farachi, C.; Ponti, F. Synthesis 1979, 617.
    • (1979) Synthesis , pp. 617
    • Santaniello, E.1    Farachi, C.2    Ponti, F.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.