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Volumn 72, Issue 5, 2007, Pages 1566-1569

Conformational and configurational dynamics of a highly fluorinated hydrazone

Author keywords

[No Author keywords available]

Indexed keywords

FLUORINATED HYDRAZONE; LEWIS BASICITY;

EID: 33847628342     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo061945n     Document Type: Article
Times cited : (16)

References (11)
  • 3
    • 0000371246 scopus 로고
    • For a general discussion of conformational and configurational isomerism in hydrazones, see
    • For a general discussion of conformational and configurational isomerism in hydrazones, see: Karabatsos, G. J.; Taller, R. A. Tetrahedron 1968, 24, 3923.
    • (1968) Tetrahedron , vol.24 , pp. 3923
    • Karabatsos, G.J.1    Taller, R.A.2
  • 4
    • 33847660213 scopus 로고    scopus 로고
    • Frisch, M. J, Trucks, G. W, Schlegel, H. B, Scuseria, G. E, Robb, M. A, Cheeseman, J. R, Zakrzewski, V. G, Montgomery, J. A, Jr, Stratmann, R. E, Burant, J. C, Dapprich, S, Millam, J. M, Daniels, A. D, Kudin, K. N, Strain, M. C, Farkas, O, Tomasi, J, Barone, V, Cossi, M, Cammi, R, Mennucci, B, Pomelli, C, Adamo, C, Clifford, S, Ochterski, J, Petersson, G. A, Ayala, P. Y, Cui, Q, Morokuma, K, Malick, D. K, Rabuck, A. D, Raghavachari, K, Foresman, J. B, Cioslowski, J, Ortiz, J. V, Stefanov, B. B, Liu, G, Liashenko, A, Piskorz, P, Komaromi, I, Gomperts, R, Martin, R. L, Fox, D. J, Keith, T, Al-Laham, M. A, Peng, C. Y, Nanayakkara, A, Gonzalez, C, Challacombe, M, Gill, P. M. W, Johnson, B. G, Chen, W, Wong, M. W, Andres, J. L, Head-Gordon, M, Replogle, E. S, Pople, J. A. Gaussian 98. revision A.5; Gaussian. Inc, Pittsburgh, PA, 1998
    • Frisch, M. J.; Trucks, G. W.; Schlegel, H. B.; Scuseria, G. E.; Robb, M. A.; Cheeseman, J. R.; Zakrzewski, V. G.; Montgomery, J. A., Jr.; Stratmann, R. E.; Burant, J. C.; Dapprich, S.; Millam, J. M.; Daniels, A. D.; Kudin, K. N.; Strain, M. C.; Farkas, O.; Tomasi, J.; Barone, V.; Cossi, M.; Cammi, R.; Mennucci, B.; Pomelli, C.; Adamo, C.; Clifford, S.; Ochterski, J.; Petersson, G. A.; Ayala, P. Y.; Cui, Q.; Morokuma, K.; Malick, D. K.; Rabuck, A. D.; Raghavachari, K.; Foresman, J. B.; Cioslowski, J.; Ortiz, J. V.; Stefanov, B. B.; Liu, G.; Liashenko, A.; Piskorz, P.; Komaromi, I.; Gomperts, R.; Martin, R. L.; Fox, D. J.; Keith, T.; Al-Laham, M. A.; Peng, C. Y.; Nanayakkara, A.; Gonzalez, C.; Challacombe, M.; Gill, P. M. W.; Johnson, B. G.; Chen, W.; Wong, M. W.; Andres, J. L.; Head-Gordon, M.; Replogle, E. S.; Pople, J. A. Gaussian 98. revision A.5; Gaussian. Inc.: Pittsburgh, PA, 1998.
  • 5
    • 33947482995 scopus 로고    scopus 로고
    • Solvents that can H-bond to the N-H hydrogen of aldehyde 2,4-dinitrophenylhydrazones increase the E/Z ratio. Karabatsos, G. J.; Shapiro, B. L.; Vane, F. M.; Fleming, J. S.; Ratka, J. S. J. Am. Chem. Soc. 1963, 85, 2784.
    • Solvents that can H-bond to the N-H hydrogen of aldehyde 2,4-dinitrophenylhydrazones increase the E/Z ratio. Karabatsos, G. J.; Shapiro, B. L.; Vane, F. M.; Fleming, J. S.; Ratka, J. S. J. Am. Chem. Soc. 1963, 85, 2784.
  • 7
    • 0003861733 scopus 로고    scopus 로고
    • 86th ed, Lide, D. R, Ed, Taylor and Francis: Boca Raton
    • CRC Handbook of Chemistry and Physics, 86th ed.; Lide, D. R., Ed.; Taylor and Francis: Boca Raton, 2005; p 15-17.
    • (2005) CRC Handbook of Chemistry and Physics , pp. 15-17
  • 10
    • 37049111062 scopus 로고    scopus 로고
    • Ab initio calculations indicate that simple hydrazones undergo E/Z isomerization via the inversion pathway. Benassi, R.; Taddei, F. J. Chem. Soc., Perkin Trans. II 1985, 1629.
    • Ab initio calculations indicate that simple hydrazones undergo E/Z isomerization via the inversion pathway. Benassi, R.; Taddei, F. J. Chem. Soc., Perkin Trans. II 1985, 1629.
  • 11
    • 84984030318 scopus 로고
    • Regarding the generality of the inversion mechanism, see:, and references therein
    • Regarding the generality of the inversion mechanism, see: Paetzold, R.; Reichenbächer, M.; Appenroth, K. Z. Chem. 1981, 21, 421 and references therein.
    • (1981) Z. Chem , vol.21 , pp. 421
    • Paetzold, R.1    Reichenbächer, M.2    Appenroth, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.