REVERSIBLE CONDENSATION OF 4-ARYLIDENE-1,2-DIMETHYL-1<i>H</i>-IMIDAZOL-5(4<i>H</i>)-ONES WITH AROMATIC ACYL CHLORIDES
DOI:
https://doi.org/10.1007/2660Keywords:
imidazolones, chromophores, fluorescent proteins, condensationAbstract
(Z)-1,2-Dimethyl-4-(4-methoxybenzylidene)-1H-imidazol-5(4H)-one underwent a condensation reaction with aromatic acyl chlorides, forming keto derivatives that were structurally similar to chromophores of red fluorescent proteins, as well as to the products of their maturation and/or degradation. The reverse reaction of the obtained products was observed upon treatment with aqueous alkali.
How to Cite
Golodukhina, S. V.; Baleev, N. S.; Mineyev, K. S.; Baranov, M. S. Chem. Heterocycl. Compd. 2015, 51, 944. [Khim. Geterotsikl. Soedin. 2015, 51, 944.]
For this article in the English edition see DOI 10.1007/s10593-015-1802-6
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Published
2015-10-29
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Letters to the Editor