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Metabolic conversion of 14C-indole-3-acetic acid to 14C-oxindole-3-acetic acid

โœ Scribed by Dennis M. Reinecke; Robert S. Bandurski


Book ID
118315296
Publisher
Elsevier Science
Year
1981
Tongue
English
Weight
314 KB
Volume
103
Category
Article
ISSN
0006-291X

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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 OxIAAยทg(-1) (dry weight) whereas ungerminated seeds contained 0.2 ngยทg(-1). Isotopically labelled OxIAA was f

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## Abstract A general method for microscale synthesis of ^14^Cโ€labeled indoleโ€3โ€acetic acids with halogen substitutions in the benzene ring is described. The method utilizes halogen substituted phenylhydrazines reacted with [^14^C]โ€2โ€oxoglutarate to generate the halogenated indoleโ€3โ€acetic acid. 3โ€

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