Journal of Organic Chemistry p. 1484 - 1489 (1990)
Update date:2022-08-10
Topics:
Singh, Satendra
Jen, Jen-Fon
Dryhurst, Glenn
The autoxidation of the indolic neurotoxin 5,6-dihydroxytryptamine has been studied in pH 7,2 phosphate buffer.The major initial product of the autoxidation has been isolated and by using spectral methods ist structure is shown to be 2,7'-bi(5,6-dihydroxytryptamine).Liquid chromatography-mass spectrometry has been used to identify two trihydroxytryptamines and a second dimer of 5,6-DHT as minor autoxidation products.
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