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The Reactivity of 2,4,6-Tirphenylpyridinium Ylids

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【Author】 Shrong Shi LIN*, Jian Mei WANG, Cheng Yong LI Department of Chemistry, Peking University, Beijing 100871

【Abstract】 Triphenylpyridinium ylid 2, generated by the decarboxylation of betaine 1, were noted to react with acetyl chloride, chloroform or acetone to form addition-elimination product and proton extraction - carbanion addition products, respectively. The reaction with chloroform was determined as pseudo first order from kinetic experiments. The values of kobsd and t1/2 for decarboxylation at 20, 40 and 50C were calculated to be 4.6 x 10-4, 8.8 x 10-3, 2.8 x 10-2 min-1 and 1.5 x 103, 78, 24 minutes, respectively.

【基金】 the National Natural Science Foundation of China (No. 20272001)
  • 【文献出处】 Chinese Chemical Letters ,中国化学快报(英文版) , 编辑部邮箱 ,2003年02期
  • 【分类号】O626
  • 【下载频次】22
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