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Acknowledgement to Reviewers of Molbank in 2018
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3-Chloro-5-(3-n-hexylthien-2-yl)-4H-1,2,6-thiadiazin-4-one
Open AccessFeature PaperShort Note

3,5-Bis[5-(thiazol-2-yl)thien-2-yl]-4H-1,2,6-thiadiazin-4-one

1
Department of Life Sciences, School of Sciences, European University Cyprus, 6 Diogenis Str., Engomi, P. O. Box 22006, 1516 Nicosia, Cyprus
2
Department of Chemistry, University of Cyprus, P. O. Box 20537, 1678 Nicosia, Cyprus
*
Author to whom correspondence should be addressed.
Molbank 2019, 2019(1), M1045; https://doi.org/10.3390/M1045
Received: 21 December 2018 / Revised: 11 January 2019 / Accepted: 13 January 2019 / Published: 15 January 2019
(This article belongs to the Special Issue Heteroatom Rich Organic Heterocycles)
Stille coupling of 3,5-bis(5-bromothien-2-yl)-4H-1,2,6-thiadiazin-4-one (10) with 2-(tri-n-butylstannyl)thiazole and Pd(Ph3P)2Cl2 in PhMe, at ca. 110 °C, for 2 h, gave 3,5-bis[5-(thiazol-2-yl)thien-2-yl]-4H-1,2,6-thiadiazin-4-one (9) in 81% yield. The latter is evaluated for its electronic properties. View Full-Text
Keywords: heterocycle; 1,2,6-thiadiazine; thiazole; Stille coupling; oligomer heterocycle; 1,2,6-thiadiazine; thiazole; Stille coupling; oligomer
MDPI and ACS Style

Kalogirou, A.S.; Koutentis, P.A. 3,5-Bis[5-(thiazol-2-yl)thien-2-yl]-4H-1,2,6-thiadiazin-4-one. Molbank 2019, 2019, M1045.

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