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Molbank 2018, 2018(4), M1024; https://doi.org/10.3390/M1024

Purine-Furan and Purine-Thiophene Conjugates

Faculty of Materials Science and Applied Chemistry, Riga Technical University, P. Valdena Str. 3, LV-1048 Riga, Latvia
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Received: 14 September 2018 / Revised: 4 October 2018 / Accepted: 5 October 2018 / Published: 8 October 2018
(This article belongs to the Section Organic Synthesis)
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Abstract

Furyl and thienyl moieties were introduced into a purine structure to elevate its fluorescence properties, while a trityl group was used to increase the amorphous properties of the purine compounds. The title compounds were prepared by a sequence involving a Mitsunobu, a SNAr and a Suzuki–Miyaura reaction and their photophysical properties were studied. Quantum yields in the solution reached up to 88% but only up to 5% in the thin layer. View Full-Text
Keywords: purine; furan conjugates; thiophene conjugates; fluorescence; Suzuki–Miyaura reaction purine; furan conjugates; thiophene conjugates; fluorescence; Suzuki–Miyaura reaction
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This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited (CC BY 4.0).

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Kapilinskis, Z.; Novosjolova, I.; Turks, M. Purine-Furan and Purine-Thiophene Conjugates. Molbank 2018, 2018, M1024.

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