Title of article
Novel α-tosyloxylation of ketones catalyzed by the in situ generated hypoiodous acid from alkyl iodide
Author/Authors
Zhang، نويسنده , , Bijun and Han، نويسنده , , Liuquan and Hu، نويسنده , , Jiantao and Yan، نويسنده , , Jie، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2014
Pages
4
From page
5851
To page
5854
Abstract
Using a catalytic amount of 1-iodopropane, a novel and efficient procedure has been developed for direct preparation of α-tosyloxyketones from ketones. In this protocol, 1-iodopropane is first oxidized into iodosylpropane, which decomposes to form the key catalyst hypoiodous acid. With this method, not only α-tosyloxyketones, but also other α-sulfonyloxyketones have been prepared in moderate to good yields, which extends the application of alkyl substituted hypervalent iodine reagents in organic synthesis.
Keywords
Iodosylalkane , ?-Tosyloxylation , Hypoiodous acid , 1-Iodopropane
Journal title
Tetrahedron Letters
Serial Year
2014
Journal title
Tetrahedron Letters
Record number
1890950
Link To Document