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85153026676
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(Jpn. Pat. 7.700.006), 1977
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For silanols see: [10a] N. Hagihara, S. Takahashi, T. Shibano (Jpn. Pat. 7.700.006), 1977; Chem. Abstr. 1977, 86, 189198k. [10b] M. Capka, P. Svoboda, J. Hetflejs, Coll. Czech. Chem. Commun. 1973, 38, 1242.
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85153002893
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note
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4 olefins are even cheaper.
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70
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0000709185
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[12a] R. Benn, P. W. Jolly, R. Mynott, B. Raspel, G. Schenker, K.-P. Schick, G. Schroth, Organometallics 1985, 4, 1945.
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[12e] P. W. Jolly. Angew. Chem. 1985, 97, 279; Angew. Chem. Int. Ed. Engl. 1985, 24, 283.
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80
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85153028475
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note
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37 mg (0.14 mmol) of triphenylphosphane and 11 mg (0.05 mmol) of palladium(II) acetate were dissolved in 56 g (1.75 mol) of methanol under argon. The mixture was transferred into a cooled (dry ice) autoclave (Parr model 4561). Subsequently, 54 g (1.00 mol) of butadiene was condensed into the autoclave and the vessel was heated to the reaction temperature. After the reaction was complete, the autoclave was cooled down and the remaining butadiene was recondensed. The conversion was determined by the mass difference of butadiene. The yields of telomerization products were determined by GC (with dodecane as an internal standard) using an HP 6869A gas chromatograph. In order to isolate the octadienyl ethers, the reaction mixture was distilled in vacuo.
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85
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85153027098
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note
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B) = 41.6Hz.
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86
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0011438965
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