Synthesis and highly efficient light-induced rearrangements of diphenylmethylene(2-benzo[b]thienyl)fulgides and fulgimides

Synthesis and highly efficient light-induced rearrangements of diphenylmethylene(2-benzo[b]thienyl)fulgides and fulgimides

2-Benzo[b]thienyl fulgides and fulgimides containing bulky diphenylmethylene substituents were synthesized in the form of their ring-opened E- or Z-isomers. In contrast to the majority of known fulgides/fulgimides, that form colored ring-closed structures under UV irradiation, the obtained compounds...

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Bibliographic Details
Main Authors: Vladimir P. Rybalkin, Sofiya Yu. Zmeeva, Lidiya L. Popova, Valerii V. Tkachev, Andrey N. Utenyshev, Olga Yu. Karlutova, Alexander D. Dubonosov, Vladimir A. Bren, Sergey M. Aldoshin, Vladimir I. Minkin
Format: Article
Language:English
Published: Beilstein-Institut 2020-07-01
Series:Beilstein Journal of Organic Chemistry
Subjects:
benzo[b]thiophene
fulgide
fulgimide
photorearrangement
x-ray diffraction
Online Access:https://doi.org/10.3762/bjoc.16.149

Internet

https://doi.org/10.3762/bjoc.16.149

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