2-Benzopyrylium salts. 34. Reactions of 3-carboxy-2-benzopyrylium salts with amines. Synthesis of cyclic ketols
โ Scribed by Yu. A. Zhdanov; V. G. Brovchenko; M. A. Klyuev; E. V. Kuznetsov
- Publisher
- Springer US
- Year
- 1989
- Tongue
- English
- Weight
- 510 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0009-3122
No coin nor oath required. For personal study only.
โฆ Synopsis
3-Carboxy-2-benzopyrylium salts form 3-carboxyisoquinolinium salts, their decarboxylated analogs, or products of contraction of the heterocycle, namely, cyclic ketols, depending on the nature of the amine and solvent. Upon treatment with acids, these ketols are demethylated through the intermediate formation of ~-acylcarbenium ions and are converted to quinonemethides.
๐ SIMILAR VOLUMES
The weak intensity of the CN stretching band in IR spectra for l-ayanoiso chromenes is obviousZy determined by the steric position of the CN group in the rroZecuZe, as it was estabUshed by X-ray structuraZ anclysis for the ayanide addition product (2d) of l-isopropyZ-3-methyZ-2-benzopyryZium sclts.