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Mendeleev Communications, 2001, Volume 11, Issue 3, Pages 90–91
DOI: https://doi.org/10.1070/MC2001v011n03ABEH001430
(Mi mendc4234)
 

This article is cited in 2 scientific papers (total in 2 papers)

Photoisomerization of 2,4,4,6-tetraaryl-4H-selenopyrans: a new heterocyclic ring contraction

J. Kroulika, J. Cejkab, P. Sebeka, P. Sedmerac, P. Haladac, V. Havlicekc, S. Nespurekd, B. Kratochvilb, J. Kuthana

a Department of Organic Chemistry, Institute of Chemical Technology, Prague, Czech Republic
b Department of Solid State Chemistry, Institute of Chemical Technology, Prague, Czech Republic
c Institute of Microbiology, Academy of Science of the Czech Republic, Prague
d Institute of Macromolecular Chemistry, Academy of Sciences of the Czech Republic, Prague, Czech Republic
Full-text PDF (116 kB) Citations (2)
Abstract: The UV illumination of title compounds 3a,b in acetonitrile solutions leads to corresponding five-membered ring isomers 4a,b, probably, via open-ring intermediates, whereas the photocolouration was observed in the solid state
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Document Type: Article
Language: English


Citation: J. Kroulik, J. Cejka, P. Sebek, P. Sedmera, P. Halada, V. Havlicek, S. Nespurek, B. Kratochvil, J. Kuthan, “Photoisomerization of 2,4,4,6-tetraaryl-4H-selenopyrans: a new heterocyclic ring contraction”, Mendeleev Commun., 11:3 (2001), 90–91
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  • This publication is cited in the following 2 articles:
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