## Abstract 3‐Pivaloyl‐2__H__‐1‐benzopyran‐2‐one (6) reacts with acid anhydrides in the presence of triethylamine to give 4‐(2‐oxoalkyl)‐2‐oxochromans 7 and 3‐pivaloyl‐2‐oxochroman (8) in moderate yields. Also 3‐propionyl‐ and 3‐isobutyryl‐2__H__‐1‐benzopyran‐2‐ones (9) react with acid anhydrides u
Cyclopropanation reaction of 3-Acyl-2H-1-benzopyran-2-ones with phenacylbromide in phase transfer systems
✍ Scribed by Anka Bojilova; Antoaneta Trendafilova; Christo Ivanov; Nestor A Rodios
- Book ID
- 108371580
- Publisher
- Elsevier Science
- Year
- 1993
- Tongue
- French
- Weight
- 819 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0040-4020
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📜 SIMILAR VOLUMES
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## Abstract magnified image The title aldehyde **1** reacts smoothly with the enamine moiety of **2**‐aminochromone **2** to produce hitherto unreported 3‐(2‐hydroxybenzoyl)‐5__H__‐1‐benzopyrano[2,3‐__b__]pyridin‐5‐one (azaxanthone) **5**. This reaction has been extended for the synthesis of bisaz