Cyclopropylcarbinyl p-Toluenesulfonate Solvolysis. 1-Ring Substituent Effect
DD Roberts
Index: Roberts,D.D. Journal of Organic Chemistry, 1965 , vol. 30, p. 23 - 28
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Citation Number: 22
Abstract
Results Each of these esters was allowed to solvolyze in the indicated solvent and the course of reaction was followed by titrating the liberated p-toluenesulfonic acid. The solvolysis reactions of cyclopropylcarbinyl tosylate in 90% acetone and sulfolane demonstrated the previously reported" internal return" rearrangement2 which accounted for about 15y0 of the starting material. The purities of the starting materials were, therefore, ...
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