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Volumn 31, Issue 2, 2011, Pages 172-182

Revisiting the mechanism of β-O-4 bond cleavage during acidolysis of lignin. Part 3: Search for the rate-determining step of a non-phenolic C 6-C3 type model compound

Author keywords

Acidolysis; alkyl aryl ether; hydride transfer; kinetic; lignin; rate determining step

Indexed keywords

1 ,4-DIOXANE; ACIDOLYSIS; ALKYL-ARYL ETHER; BOND CLEAVAGES; C-H BOND; CORRESPONDING COMPOUNDS; ENOL ETHERS; GUAIACYL; HYDRIDE TRANSFER; HYDRIDE TRANSFERS; KINETIC ISOTOPE EFFECTS; LIGNIN MODEL COMPOUND; MODEL COMPOUND; RATE DETERMINING STEP;

EID: 79957626303     PISSN: 02773813     EISSN: 15322319     Source Type: Journal    
DOI: 10.1080/02773813.2010.515050     Document Type: Article
Times cited : (42)

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    • Revisiting the mechanism of â-O-4 bond cleavage during acidolysis of lignin. Part 2: Detailed reaction mechanism of a non-phenolic C6-C2 type model compound
    • accepted
    • Yokoyama T, Matsumoto Y. Revisiting the mechanism of â-O-4 bond cleavage during acidolysis of lignin. Part 2: Detailed reaction mechanism of a non-phenolic C6-C2 type model compound. J. Wood Chem. Technol. (accepted).
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.