A short and facile synthetic route to prenylated flavones. Cyclodehydrogenation of prenylated 2′-hydroxychalcones by a hypervalent iodine reagent
✍ Scribed by Katalin Gula´csi; Gyo¨rgy Litkei; Sa´ndor Antus; Tama´s E. Gunda
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 443 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0040-4020
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✦ Synopsis
The first synthesis of the prenylated flavones kanzonoI-D (1), -E (3) and yinyanghuo-C (4) was accomplished by cyclodehydrogenation of the appropriately substituted 2'-hydroxychalcones 16, 14 and 11, respectively, in presence of phenyliodine(III) diacetate (PIDA) / potassium hydroxide m methanol. The synthesis of kanzonoI-B (13) was also achieved from the 2'-hydroxychalcone 12.
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