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Oxindoles. New, general method of synthesis

โœ Scribed by Gassman, Paul G.; Van Bergen, T. J.


Book ID
115507658
Publisher
American Chemical Society
Year
1974
Tongue
English
Weight
664 KB
Volume
96
Category
Article
ISSN
0002-7863

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๐Ÿ“œ SIMILAR VOLUMES


Oxindoles. New, general method of synthe
โœ Gassman, Paul G.; Van Bergen, T. J. ๐Ÿ“‚ Article ๐Ÿ“… 1974 ๐Ÿ› American Chemical Society ๐ŸŒ English โš– 664 KB

and dried over anhydrous mtlgnesium sulfate. The drying agent was removed by filtration, and the solvent was evaporated to give 10.50 g (84% yield) of 61 as a light yellow oil: ir (neat) 3380 (enamine NH), 3050-2850 (CH), 1735 (ester C=O), 1670 (C==N), and 1615 (C==C) cm-l; pmr (CCI,) 2.80-3.50 (4 H

New synthesis of oxindole-1-carboxamides
โœ Marta Porcs-Makkay; Gyula Simig ๐Ÿ“‚ Article ๐Ÿ“… 2001 ๐Ÿ› Journal of Heterocyclic Chemistry ๐ŸŒ English โš– 47 KB

## Abstract A new synthesis of oxindoleโ€1โ€carboxamides was elaborated by the reaction of oxindoleโ€1โ€phenylโ€carboxylate with various amines. This method also permitted the preparation of __N,N__โ€disubstituted oxindoleโ€1โ€carboxamides.