Progress in Drug Research / Fortschritte Der Arzneimittelforschung / Progrès Des Recherches Pharmaceutiques 1963
DOI: 10.1007/978-3-0348-7050-4_3
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Physico Chemical Methods in Pharmaceutical Chemistry I. Spectrofluorometry

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1964
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Cited by 2 publications
(3 citation statements)
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“…However, it has recently been claimed that 4-and 7-hydroxyindole fluoresce when activated in the 288-290 my range (9). Under these conditions solutions of 4-and 7-hydroxyindole in methanol showed maximum fluorescence a t 312 mp and 315 my respectively (9). So far, very few investigators have described work which deals with the fluorescence characteristics of the hydrogen sulfate esters of the hydroxyindoles.…”
Section: R a Heacock~ And 0 Hut Zinger^mentioning
confidence: 97%
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“…However, it has recently been claimed that 4-and 7-hydroxyindole fluoresce when activated in the 288-290 my range (9). Under these conditions solutions of 4-and 7-hydroxyindole in methanol showed maximum fluorescence a t 312 mp and 315 my respectively (9). So far, very few investigators have described work which deals with the fluorescence characteristics of the hydrogen sulfate esters of the hydroxyindoles.…”
Section: R a Heacock~ And 0 Hut Zinger^mentioning
confidence: 97%
“…3630 my, while the corresponding 4-and 7-hydrsxytryptamines and 7-hydroxy-3-indolylacetic acid apparently did not fluoresce under these conditions (8). However, it has recently been claimed that 4-and 7-hydroxyindole fluoresce when activated in the 288-290 my range (9). Under these conditions solutions of 4-and 7-hydroxyindole in methanol showed maximum fluorescence a t 312 mp and 315 my respectively (9).…”
Section: R a Heacock~ And 0 Hut Zinger^mentioning
confidence: 98%
See 1 more Smart Citation