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Stelzer, O.7
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and references cited therein
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In: Fréchet J.M.J., and Tomalia D.A. (Eds). Dendrimers and Other Dendritic Polymers (2001), John Wiley & Sons, New York
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37
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0011448752
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Previously reported phosphine core dendrimers:
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Previously reported phosphine core dendrimers:. Oosterom G.E., Steffens S., Reek J.N.H., Kamer P.C.J., and van Leeuwen P.W.N.M. Top. Catal. 19 (2002) 61-73
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Oosterom, G.E.1
Steffens, S.2
Reek, J.N.H.3
Kamer, P.C.J.4
van Leeuwen, P.W.N.M.5
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0035843054
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Balaji B.S., Obora Y., Ohara D., Koide S., and Tsuji Y. Organometallics 20 (2001) 5342-5350
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Balaji, B.S.1
Obora, Y.2
Ohara, D.3
Koide, S.4
Tsuji, Y.5
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40
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34548042920
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note
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2O: C, 69.74; H, 4.77. Found: C, 69.80; H, 4.74.
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41
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33748787121
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2H]): -10.68 ppm, palladium complex: 19.35 ppm. This downfield shift is similar to that reported in the literature:
-
2H]): -10.68 ppm, palladium complex: 19.35 ppm. This downfield shift is similar to that reported in the literature:. Iwasawa T., Komano T., Tajima A., Tokunaga M., Obora Y., Fujihara T., and Tsuji Y. Organometallics 25 (2006) 4665-4669
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Organometallics
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Iwasawa, T.1
Komano, T.2
Tajima, A.3
Tokunaga, M.4
Obora, Y.5
Fujihara, T.6
Tsuji, Y.7
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42
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34548046148
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note
-
2K])-palladium aqueous solution at 0 °C. The resulting mixture was stirred for 4 h at 50 °C. The reaction mixture was subjected to the usual extractive workup with diethyl ether. The residual oil obtained after evaporation of diethyl ether, which was dried over magnesium sulfate, was purified by column chromatography on silica gel to give the coupling product 7.
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43
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0034596298
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The dispersion system was stable within several minutes. Quick measurement (SEM) of this system indicated that its particle size was 1 μm. Kobayashi et al. have also reported that Lewis acid-surfactant-combined catalyst systems form colloidal dispersions (not micelle):
-
The dispersion system was stable within several minutes. Quick measurement (SEM) of this system indicated that its particle size was 1 μm. Kobayashi et al. have also reported that Lewis acid-surfactant-combined catalyst systems form colloidal dispersions (not micelle):. Manabe K., Mori Y., Wakabayashi T., Nagayama S., Kobayashi S. J. Am. Chem. Soc. 122 (2000) 7202-7207
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J. Am. Chem. Soc.
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Manabe, K.1
Mori, Y.2
Wakabayashi, T.3
Nagayama, S.4
Kobayashi, S.5
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44
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34548037353
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-
note
-
2, which was not a dendritic catalyst, the catalytic reaction did not proceed.
-
-
-
-
45
-
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34548051264
-
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note
-
TPPTS: triphenylphosphine-3,3′,3″-trisulfonic acid trisodium salt.
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-
-
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46
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27744472602
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Previously reported positive dendritic effects on chemical yields caused by the periphery-catalyzed dendrimers:
-
Previously reported positive dendritic effects on chemical yields caused by the periphery-catalyzed dendrimers:. Benito J.M., de Jesus E., de la Mata F.J., Flores J.C., and Gomez R. Chem. Commun. (2005) 5217-5219
-
(2005)
Chem. Commun.
, pp. 5217-5219
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-
Benito, J.M.1
de Jesus, E.2
de la Mata, F.J.3
Flores, J.C.4
Gomez, R.5
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