Reinvestigation of dimerization of Z-N-alkylarylmethylideneindoxyls upon exposure to UV-vis radiation View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2017-02

AUTHORS

O. L. Babii, A. A. Hodak, A. S. Peregudov, V. I. Polshakov, Z. A. Starikova, Yu. A. Borisov, Yu. V. Fedorov, V. S. Velezheva

ABSTRACT

N-Alkyl-2-arylmethylideneindoxyls upon exposure to UV or visible light undergo dimerization not to cyclobutane adducts as it has been reported earlier, but to spiropyrano[3,2-b]-pseudoindoxyls with a spiropseudoindoxyl fragment characteristic of many natural alkaloids. The structure of spiropyranopseudoindoxyls was established by NMR spectroscopy and X-ray crystallography.

PAGES

350-354

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11172-017-1739-2

DOI

http://dx.doi.org/10.1007/s11172-017-1739-2

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1090364732


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