Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1389252 | Carbohydrate Research | 2010 | 6 Pages |
Abstract
Vicenin-3 was synthesized from naringenin via a short five-step reaction, which included two regioselective direct C-glycosylations with d-glucose and d-xylose (yields: 22% and 30%, respectively) as the key reactions for a total yield of 4.4%. Vicenin-1 was also synthesized from phloroacetophenone via a 10-step reaction, including the same glycosylation described above, for a total yield of 2.7% with a vicenin-3 yield of 1.7%.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Shingo Sato, Tomoyuki Koide,