| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5280092 | Tetrahedron Letters | 2007 | 6 Pages |
Abstract
A new fluorous benzylidene acetal protecting group was regioselectively introduced into carbohydrates, deprotected under acidic conditions, and reused. Oligosaccharides were synthesized via regioselective conversion of the fluorous acetal group to the benzyl group by traditional reaction conditions. The fluorous compounds were easily separated from non-fluorous by-products by fluorous solid phase extraction.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Masaru Kojima, Yutaka Nakamura, Seiji Takeuchi,