期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 74, 期 17, 页码 6891-6894出版社
AMER CHEMICAL SOC
DOI: 10.1021/jo900457k
关键词
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资金
- JSPS [20.1219]
- Ministry of Education, Science, Sports, and Culture [21350009, 461]
- Grants-in-Aid for Scientific Research [21350009] Funding Source: KAKEN
Thermal conversion of methyl. beta-D-glucoside to levoglucosan was studied with the MP4//DFT(B3LYP) method. The first step is conformational change of the reactant to C-1(4) from C-4(1). The second step is intramolecular nucleophilic substitution at the anomeric Cl, which occurs via one step without oxacarbenium ion intermediate. The Delta G(0 double dagger) value (52.5 kcal/mol) is smaller than the Cl-Ol bond energy, indicating the direct homolysis mechanism is clearly ruled out. Bimolecular reaction also occurs with smaller activation energy via the similar transition state.
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