Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1389183 | Carbohydrate Research | 2007 | 6 Pages |
Abstract
The transformation of d-xylose and l-arabinose, the two major components of wheat straw and bran, into a unique multifunctional, optically pure, five-carbon synthon has been achieved. The synthetic sequence requires three steps: suitable protection of the hydroxyl groups of the pentoses, introduction of an iodide at the C-5 position and zinc-mediated opening of the furanose ring leading to the formation of a common substituted pent-4-enal.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Ariane Bercier, Richard Plantier-Royon, Charles Portella,