Benzenoid-quinonoid tautomerism in azomethines and their structural analogs 45. 3-Hydroxy-2-acetyl-1-methylindole imines View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1989-06

AUTHORS

E. N. Shepelenko, A. D. Dubonosov, A. E. Lyubarskaya, V. A. Bren', V. I. Minkin

ABSTRACT

Some 3-hydroxy-2-acetyl-1-methylindole N-aryl- and N-alkylimines have been obtained. According to UV and IR spectroscopy, they exist as the acoplanar E-ketoenamine isomers. Structural relaxation in the excited state results in the formation of flattened, fluorescing forms.

PAGES

639-642

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf00470021

DOI

http://dx.doi.org/10.1007/bf00470021

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1008725832


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