𝔖 Bobbio Scriptorium
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4-Hydroxylindole-acetic acid — The microbiological transformation product of indole-3-acetic acid

✍ Scribed by A. G. Kozlovskii; K. A. Koshcheenko; M. U. Arinbasarov; T. G. Baklashova; V. M. Adanin; G. I. Yakovlev

Book ID
112438148
Publisher
Springer
Year
1975
Tongue
English
Weight
348 KB
Volume
24
Category
Article
ISSN
1573-9171

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Indole-3-Acetic Acid and Flowering
Indole-3-Acetic Acid and Flowering
✍ GREEN, M.; FULLER, H. J. 📂 Article 📅 1948 🏛 American Association for the Advancement of Scienc 🌐 English ⚖ 149 KB
Comparative ab initio SCF conformational
Comparative ab initio SCF conformational study of 4-chloro-indole-3-acetic acid and indole-3-acetic acid phytohormones (auxins)
✍ Michael Ramek; Sanja Tomić; Biserka Kojić-Prodić 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 516 KB

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

Identification of oxindole-3-acetic acid
Identification of oxindole-3-acetic acid, and metabolic conversion of indole-3-acetic acid to oxindole-3-acetic acid inPinus sylvestrisseeds
✍ Arild Ernstsen; Göran Sandberg; Karin Lundström 📂 Article 📅 1987 🏛 Springer-Verlag 🌐 English ⚖ 516 KB

Oxindole-3-acetic acid (OxIAA) has been identified in germinating seeds of Scots pine (Pinus sylvestris) using gas chromatography-mass spectrometry. Seeds germinated for 5 d contained 2.7 ng OxIAA·g(-1) (dry weight) whereas ungerminated seeds contained 0.2 ng·g(-1). Isotopically labelled OxIAA was f

Colorimetric estimation of indole-3-acet
Colorimetric estimation of indole-3-acetic acid
✍ Joseph Chrastil 📂 Article 📅 1976 🏛 Elsevier Science 🌐 English ⚖ 354 KB

After oxidation of indole-3-acetic acid with ceric nitrate in the presence of hydroxylamine, a stable colored complex extractable to isoamyl alcohol is formed. This reaction is useful for the calorimetric estimation of indole-3-acetic acid in biological mixtures. The colored complex (whose chromopho