Preparation of 4-hydroxy-3-substituted, 2H-1-benzopyran-2-ones and 2H-1-benzothiopyran-2-ones from carboxylic esters and methyl salicylates or methyl thiosalicylate
โ Scribed by Sharon E. Davis; A. Cameron Church; Rebecca C. Tummons; Charles F. Beam
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1997
- Tongue
- English
- Weight
- 305 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0022-152X
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โฆ Synopsis
Abstract
C(ฮฑ)โCarboxylic acid esters were treated with excess lithium diisopropylamide, condensed with methyl salicylates or methyl thiosalicylate, followed by acid cyclization to either 4โhydroxyโ3โsubstituted, 2__H__โ1โbenzopyranโ2โones (coumarins), or 2__H__โ1โbenzothiopyranโ2โones (thiocoumarins).
๐ SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
substituted 4-methylcoumarins (4-methyl-2H-1 -benzopyran-2-ones) have been recorded. The effects of an alkyl side-chain at C-3 on the chemical shift values and that of a methoxy or an acetoxy group