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Holler, M.1
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3
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0343615644
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M. Holler, D. Tritsch, J.-F. Biellmann, unpublished results
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M. Holler, D. Tritsch, J.-F. Biellmann, unpublished results.
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4
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0027168350
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M. Holler, A. Burger, D. Tritsch, J.-F. Biellmann, Tetrahedron Lett. 1993, 34, 3291-3292.
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Holler, M.1
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6
-
-
0342310707
-
-
note
-
1H NMR spectroscopy, whereby vicinal typical coupling constants for the olefinic protons of 15 to 15.5 Hz and of 11 Hz were measured for E and for Z isomers. respectively.
-
-
-
-
8
-
-
0004700004
-
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b) G. Marchese, G. J. Modena, F. Naso, Tetrahedron 1968, 24, 663-674;
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Marchese, G.1
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0000543754
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b) H. Suhr, Chem. Ber. 1963, 97, 3268-3276;
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Suhr, H.1
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19
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84981625484
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A. M. van Leusen, B. A. Reith, A. J. W. Iedema, J. Strating, Recl. Trav. Chim. Pays-Bas 1972, 91, 37-49.
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Van Leusen, A.M.1
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Strating, J.4
-
20
-
-
0343180270
-
-
note
-
1H NMR spectroscopy, whereby vicinal typical coupling constants for the olefinic protons of 15.5 to 16.5 Hz and of 11 Hz were measured for E and for Z isomers, respectively.
-
-
-
-
21
-
-
0342745639
-
-
Complexes of iodoacetylenes and of hexamethylbenzene with triphenylphosphane oxide have been detected previously. a) C. Laurence, M. Queignec-Cabanetos, B. Woijtkowiak, J. Chem. Soc. Perkin II 1982, 1605-1610; b) R. A. Shaw, B. C. Smith, C. P. Thakur, Liebigs Ann. Chem. 1968, 713, 30-39.
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Laurence, C.1
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Woijtkowiak, B.3
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22
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84982341291
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Complexes of iodoacetylenes and of hexamethylbenzene with triphenylphosphane oxide have been detected previously. a) C. Laurence, M. Queignec-Cabanetos, B. Woijtkowiak, J. Chem. Soc. Perkin II 1982, 1605-1610; b) R. A. Shaw, B. C. Smith, C. P. Thakur, Liebigs Ann. Chem. 1968, 713, 30-39.
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Shaw, R.A.1
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Thakur, C.P.3
-
24
-
-
0343615617
-
-
note
-
The UV/Vis spectrum of compounds 26 and 27 could not be recorded in methanol due to their instability in this solvent.
-
-
-
-
28
-
-
0343615614
-
-
note
-
1H NMR spectrum of the selenoether 33.
-
-
-
-
30
-
-
0343615613
-
-
note
-
3, 2 < θ < 25°, 2480 data collected, 1537 observed [I > 3σ(I)]. Full matrix least squares on F; final results: R = 0.033, Rw = 0.044, GOF = 1.188.
-
-
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31
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0000322640
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T. Iijima, S. Tsuchiya, B. Kimura, Bull. Chem. Soc. Jpn. 1977, 50, 2564-2567.
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Iijima, T.1
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35
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0003942864
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Wiley, New York
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Eliel, E.E.1
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36
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0000998809
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and references cited therein
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A. Abbotto, S. Bradamante, N. Capri, H. Rzepa, D. J. Williams, A. White, J. Org. Chem. 1996 , 61, 1770-1778 and references cited therein.
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0003960770
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38
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0030908810
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Sin, H.S.1
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40
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0342310673
-
-
note
-
The absorption maximum around 360 nm is characteristic of a 4-(thiovinyl)pyridinium compound. For instance, 1-methyl-4-[2-(N-propylamino)-1-ethenyl]pyridinium iodide showed an intense absorption band centered at 390 nm in methanol. Preparation and physical properties of this compound and other related amino-related compounds will be described in another publication.
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44
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0000189906
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M. Friedman, J. F. Cavins, J. S. Wall, J. Am. Chem. Soc. 1965, 87, 3672-3682.
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0343180262
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0024970126
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0015898199
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52
-
-
0342310667
-
-
note
-
1H NMR signal intensity is relative to each isomer.
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-
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