前往化源商城

Tetrahedron letters

para-toluenesulfonyl iodide as a convenient, mild reagent for the preparation of functionalised cyclic ethers

GL Edwards, KA Walker

文献索引:Edwards, Gavin L.; Walker, Katherine A. Tetrahedron Letters, 1992 , vol. 33, # 13 p. 1779 - 1782

全文:HTML全文

被引用次数: 6

摘要

Abstract Free radical addition of para-toluenesulfonyl iodide to alkenols occurs readily to give functionalised β-iodosulfones as single regioisomers. Cyclisation to give cyclic ethers is effected by treatment with potassium carbonate in methanol. An anomalous reaction, where a substituted alkenol cyclises directly to give an iodotetrahydropyran, is also discussed.