| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1390984 | Carbohydrate Research | 2006 | 5 Pages |
Abstract
A modified synthesis of 1l-1,2:3,4-di-O-cyclohexylidene-5-O-methyl-chiro-inositol has been accomplished that improves the overall procedure, yield, and environmental aspects of its formation. Several inositol analogues have been prepared from this intermediate for testing as biosynthetic inhibitors of glycosyl-phosphatidylinositol (GPI) anchor formation.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Sylvia M. Baars, John O. Hoberg,