An ab initio conformational analysis of 4-chloroindole-3-acetic acid was performed at the RHF/6-311G \* \* level. The mirror symmetrical conformer (in which the indole ring is coplanar with the COOH group) is most stable; next in energy are the two conformers with the C-COOH fragment perpendicular t
Effect of caffeic and p-coumaric acids on indole-3-acetic acid catabolism
β Scribed by F. Tafuri; M. Businelli; L. Scarponi
- Publisher
- John Wiley and Sons
- Year
- 1972
- Tongue
- English
- Weight
- 388 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0022-5142
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## Abstract The kinetics of oxidation of indoleβ3βacetic acid (IAA) by peroxodisulfate (PDS) has been carried out in aqueous acetic acid medium. Firstβorder dependence of rate each with respect to [IAA] and [PDS] was observed. The reaction rate was unaffected by added [H^+^]. Increase of percentage