节点文献
The Reactivity of 2,4,6-Tirphenylpyridinium Ylids
【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.
【关键词】 Pyridinium ylid;
pyridinium betaine;
4-H pyridine;
kinetic experiment.;
【Key words】 Pyridinium ylid; pyridinium betaine; 4-H pyridine; kinetic experiment.;
【Key words】 Pyridinium ylid; pyridinium betaine; 4-H pyridine; kinetic experiment.;
【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