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Volumn , Issue 8, 2000, Pages 1825-1832

Palladium-catalyzed reactions for the synthesis of fine chemicals, 14([≠]) control of chemo- and regioselectivity in the palladium-catalyzed telomerization of butadiene with methanol - Catalysis and mechanism

Author keywords

Butadiene; Homogeneous catalysis; Palladium; Telomerization

Indexed keywords

BUTADIENE; CATALYSIS; PALLADIUM COMPOUNDS; REACTION INTERMEDIATES; REGIOSELECTIVITY; SYNTHESIS (CHEMICAL);

EID: 0343193157     PISSN: 14341948     EISSN: None     Source Type: Journal    
DOI: 10.1002/1099-0682(200008)2000:8<1825::aid-ejic1825>3.3.co;2-x     Document Type: Article
Times cited : (78)

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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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    • note
    • B) = 41.6Hz.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.