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α-羰基环十二酮的酮-烯醇互变异构中的构象效应
引用本文:杨晓亮,王明安,梁晓梅,王小芳,尤田耙,王道全.α-羰基环十二酮的酮-烯醇互变异构中的构象效应[J].有机化学,2005,25(10):1279-1282.
作者姓名:杨晓亮  王明安  梁晓梅  王小芳  尤田耙  王道全
作者单位:1. 南京大学化学系
2. 中国农业大学应用化学系,北京,100094
3. 北京大学医学中心药学院,北京,100083
4. 中国科学技术大学化学系,合肥,230026
摘    要:利用1H NMR技术研究了α-羰基环十二酮的酮-烯醇互变异构. 结果表明, 取代基、温度和溶剂对互变异构的影响与已知的规律一致, 但是烯醇的含量与相应的α-羰基环己酮相比要低得多, 利用构象效应对其进行了合理的解释.

关 键 词:酮-烯醇互变异构  α-羰基环十二酮  构象效应
收稿时间:11 11 2004 12:00AM
修稿时间:04 19 2005 12:00AM

Conformational Effect on the Keto-enol Tautomerism of α-Carbonylcyclododecanones
YANG,Xiao-Liang,WANG,Ming-An,LIANG,Xiao-Mei,WANG,Xiao-Fang,YOU,Tian-Ba,WANG,Dao-Quan.Conformational Effect on the Keto-enol Tautomerism of α-Carbonylcyclododecanones[J].Chinese Journal of Organic Chemistry,2005,25(10):1279-1282.
Authors:YANG  Xiao-Liang  WANG  Ming-An  LIANG  Xiao-Mei  WANG  Xiao-Fang  YOU  Tian-Ba  WANG  Dao-Quan
Institution:( Department of Applied Chemistry, China Agricultural University, Beijing 100094)( Department of Chemistry, University of Science and Technol-ogy, Hefei 230026)( School of Pharmaceutical Science, Peking Univer-sity, Beijing 100083)
Abstract:The keto-enol tautomerism of α-carbonylcyclododecanones has been studied by means of 1H NMR technology. The result shows that the effects of substituent, temperature and solvent on the tautomerism agreed with the known rules, while their enol contents were much lower than those of the corresponding α-carbonylcyclohexanones, which is illustrated reasonably by the conformational effect.
Keywords:keto-enol tautomerism  α-carbonylcyclododecanone  conformational effect
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