| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5289642 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
An efficient selective deprotection followed by acetylation of several benzyl ethers, including 6-OBn ethers of monosaccharides, and -OTBDMS ethers has been developed by using the BF3·Et2O-NaI-Ac2O reagent system. In addition, both benzylidene and isopropylidene groups are deprotected to form the corresponding diacetates.
Related Topics
Physical Sciences and Engineering
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Authors
Anita Brar, Yashwant D. Vankar,