| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5274278 | Tetrahedron Letters | 2012 | 5 Pages |
Abstract
An effective deprotection methodology of dioxolanes was developed, affording moderate to excellent yield via a LTMP-promoted reaction in THF, which displays admirable chemoselectivity in the presence of dimethylketal, 1,3-dioxane, 1,3-dithiane, or other acid-sensitive protective groups.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Changchun Yuan, Li Yang, Guizhou Yue, Tianzi Yu, Weiming Zhong, Bo Liu,