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2-Benzopyrylium salts. 34. Reactions of 3-carboxy-2-benzopyrylium salts with amines. Synthesis of cyclic ketols

โœ 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

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โœฆ 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.


๐Ÿ“œ SIMILAR VOLUMES


2-benzopyrylium salts. XXXVII. Oxygen an
โœ Irina V. Shcherbakova; Evghenii V. Kuznetsov; Iosif A. Yudilevich; Olga E. Kompa ๐Ÿ“‚ Article ๐Ÿ“… 1988 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 465 KB

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.