| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1385152 | Carbohydrate Research | 2008 | 4 Pages |
Abstract
Benzylidenation of readily available 1,5-anhydro-d-hex-1-en-3-ulose, followed by sodium borohydride reduction, afforded the title compounds in high yields. Separation of 4,6-O-benzylidene-d-allal and -d-glucal was accomplished by selective acetylation with lipase PS.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Tohru Sakakibara, Tsubasa Ito, Chika Kotaka, Yasuhiro Kajihara, Yuhya Watanabe, Aki Fujioka,