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0000360473
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J. Luo, H. Hart, J. Org. Chem. 1987, 52, 4833-4836; J. L. Segura, N. Martin, Chem. Rev. 1999, 99, 3199-3246.
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J. Luo, H. Hart, J. Org. Chem. 1987, 52, 4833-4836; J. L. Segura, N. Martin, Chem. Rev. 1999, 99, 3199-3246.
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Segura, J.L.1
Martin, N.2
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0142223636
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note
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1H NMR spectrum of the mixture of products after DDQ dehydrogenation. This product is expected to show two signals for the bridgehead protons according to its symmetry.
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109
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0142254739
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note
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A nonlinear regression analysis of Equation (3) (see Experimental Section) was performed by the use of the program TableCurve 4.0, SPSS Science analogous to the computer program HOSTEST by C. S. Wilcox, N. M. Glagovich, University of Pittsburg and the program Associate V1.6, B. Peterson, Ph. D.
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110
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note
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We thank one of the reviewers to focus our attention on the complex stoichiometries and suggesting the Job-plot analysis.
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111
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0142192540
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note
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Titration experiments were performed on a TAM 2277 microcalorimeter (Thermometric, Järfälla, Sweden) using the ampoule unit 2277-201. The addition of the solution during the titration experiment was managed with syringe-pump 6120-031, Lund, Sweden.
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112
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0142192541
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1H NMR spectrum of the 2:1 mixture of 4 and 32 also shows temperature-dependent behavior, comparable to that of a 2:1 mixture of 2 and 32. This will be reported separately, with respect to the kinetic stability of these host - guest complexes and the mobility of the guest molecules inside host cavity.
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113
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0038762733
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Wavefunction, Inc., 18401 Von Karman, Suite 370, Irvine, California 92715
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SPARTAN 02, Wavefunction, Inc., 18401 Von Karman, Suite 370, Irvine, California 92715.
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SPARTAN 02
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114
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0036708550
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C. Ochsenfeld, F. Koziol, S. P. Brown, T. Schaller, U. P. Seelbach, F.-G. Klärner, Solid State Nucl. Mag. Reson. 2002, 22, 128-153.
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Ochsenfeld, C.1
Koziol, F.2
Brown, S.P.3
Schaller, T.4
Seelbach, U.P.5
Klärner, F.-G.6
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115
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0142161652
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unpublished results
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C. Ochsenfeld et al., unpublished results.
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Ochsenfeld, C.1
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0001522501
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simplified by M Kamieth Diplomarbeit Universität Essen
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Compound 8 can be obtained from indene in four steps according to D. N. Butler, R. A. Snow, Can. J. Chem. 1975, 53, 256-262 (simplified by M. Kamieth, Diplomarbeit, Universität Essen, 1995).
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Butler, D.N.1
Snow, R.A.2
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