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1
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63849112168
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Israel Academy of Sciences and Humanities
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Jerusalem Symposium on Quantum Chemistry and Biochemistry, vol. 3, Aromaticity, Pseudoaromaticity, Antiaromaticity, Israel Academy of Sciences and Humanities, 1971
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(1971)
Jerusalem Symposium on Quantum Chemistry and Biochemistry, Aromaticity, Pseudoaromaticity, Antiaromaticity
, vol.3
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-
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3
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0035353541
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and references therein It was explicitly shown that the π electrons in naphthalene are distortive: -1419
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T. M. Krygowski M. K. Cyránski Chem. Rev. 2001 101 1385 1419
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(2001)
Chem. Rev.
, vol.101
, pp. 1385
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Krygowski, T.M.1
Cyránski, M.K.2
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15
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33947217502
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-
National Institute of Advanced Industrial Science and Technology (AIST), Japan
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NMR chemical shifts are taken from the Spectral Dataset for Organic Compounds SDBS, National Institute of Advanced Industrial Science and Technology (AIST), Japan, 2008 (http://riodb01.ibase.aist.go.jp/sdbs/cgi-bin/cre-index. cgi?lang=eng)
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(2008)
Spectral Dataset for Organic Compounds SDBS
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25
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0000296436
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R. P. Thummel, JAI Press Inc., Greenwich, CT, USA, 209-260 To see this effect in operation, see, for example, the oxidation of vitamin E derivatives:
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N. L. Frank and J. S. Siegel, in Advances in Theoretically Interesting Molecules, ed., R. P. Thummel, JAI Press Inc., Greenwich, CT, USA, 1995, vol. 3, pp. 209-260
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(1995)
Advances in Theoretically Interesting Molecules, Ed.
, vol.3
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Frank, N.L.1
Siegel In, J.S.2
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30
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33748211456
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-317
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R. Boese D. Bläser W. E. Billups M. M. Haley A. H. Maulitz D. L. Mohler K. P C. Vollhardt Angew. Chem., Int. Ed. Engl. 1994 33 313 317
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(1994)
Angew. Chem., Int. Ed. Engl.
, vol.33
, pp. 313
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Boese, R.1
Bläser, D.2
Billups, W.E.3
Haley, M.M.4
Maulitz, A.H.5
Mohler, D.L.6
Vollhardt K, P.C.7
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31
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63849334923
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For the distortive effect of the π system in benzene derivatives (e.g., 5) see: -2422
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H.-B. Bürgi K. K. Baldridge K. Hardcastle N. L. Frank P. Gantzel J. S. Siegel J. Ziller Angew. Chem., Int. Ed. Engl. 1995 34 2419 2422
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(1995)
Angew. Chem., Int. Ed. Engl.
, vol.34
, pp. 2419
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Bürgi, H.-B.1
Baldridge, K.K.2
Hardcastle, K.3
Frank, N.L.4
Gantzel, P.5
Siegel, J.S.6
Ziller, J.7
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45
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84962374078
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John Wiley & Sons Inc., Hoboken, NJ, USA, 97-103 See:
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See, for example, the summary of a chapter that discusses bond localization in aromatic compounds in: S. M. Bachrach, Computational Organic Chemistry, John Wiley & Sons Inc., Hoboken, NJ, USA, 2007, pp. 97-103
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(2007)
Computational Organic Chemistry
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Bachrach, S.M.1
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48
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0141917879
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National Institute of Standards and Technology (NIST)
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All experimental data are taken from the NIST Chemistry WebBook, National Institute of Standards and Technology (NIST), 2008 (http://webbook.nist.gov/ chemistry/)
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(2008)
NIST Chemistry WebBook
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