Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1390910 | Carbohydrate Research | 2006 | 5 Pages |
Abstract
2,3,4,6-Tetra-O-methyl-d-galactonic acid (5) was readily prepared from d-galactono-1,4-lactone (1) in 47% yield. The sequence involves tritylation of HO-6 of 1, followed by O-permethylation and deprotection. Lactonization of 5 led to the per-O-methyl-d-galactono-1,6-lactone, which was copolymerized with ε-caprolactone by ring-opening polymerization catalyzed by scandium triflate. The incorporation of the sugar comonomer into the polyester chain was about 10%.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
C. Lorena Romero Zaliz, Oscar Varela,