Iodine induced transformations of alcohols under solvent-free conditions
G Stavber, M Zupan, S Stavber
Index: Stavber, Gaj; Zupan, Marko; Stavber, Stojan Tetrahedron Letters, 2006 , vol. 47, # 48 p. 8463 - 8466
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Citation Number: 21
Abstract
Iodine has been shown to be an efficient catalyst for transformations of alcohols under solvent-free conditions. In the presence of 5% of iodine, tertiary alcohols underwent dehydration forming the corresponding alkenes, while in the case of 2-phenylpropane-2-ol cyclodimerisation to 1, 1, 3-trimethyl-3-phenylindane took place. Secondary and primary benzyl alcohols under the same conditions gave the corresponding ethers.
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