C
Constantinos A. Tsoleridis
Researcher at Aristotle University of Thessaloniki
Publications - 110
Citations - 1218
Constantinos A. Tsoleridis is an academic researcher from Aristotle University of Thessaloniki. The author has contributed to research in topics: Chromone & One-pot synthesis. The author has an hindex of 17, co-authored 110 publications receiving 1112 citations.
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Journal ArticleDOI
Expeditious One-Pot Synthesis of Highly Substituted Thiazolo[3,2-a]pyridines Involving Chromones.
Michael A. Terzidis,Julia Stephanidou-Stephanatou,Constantinos A. Tsoleridis,A. Terzis,Catherine P. Raptopoulou,Vassilis Psycharis +5 more
TL;DR: The 1,4-zwitterion derived from 4,5-dimethylthiazole and acetylenedicarboxylates has been shown to react at low temperature readily with 3-formylchromones (chromone-3-carboxaldehydes) resulting, after an unusual rearrangement, in the facile synthesis of thiazolo[3,2-a]pyridine derivatives; in the case of electron-donating substituents in the chromone ring tetracyclic chromenothiazolopyr
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Diels‐alder adducts of a spirocyclopentenotriazoloazodienophile. Assignment of their 1H and 13C NMR spectra
Nicholas E. Alexandrou,G. E. Mertzanos,Julia Stephanidou-Stephanatou,Constantinos A. Tsoleridis +3 more
TL;DR: In this article, the 1H and 13C-nmr chemical shifts as well as the relative configuration of these adducts were assigned with the help of 2D (1H-1H COSY, 1H- 1H NOESY, 2H-13C XHCORR and 1H -13C COLOC) and NOE difference spectroscopy.
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One Pot Synthesis of Aryldiazepinothiophenones
TL;DR: Aryldiazepinothiophenones were obtained from the reaction of o-phenylenediamines with acetone in the presence of 2-mercaptopropionic acid.
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Azodicarboxylates: Valuable Reagents for the Multicomponent Synthesis of Novel 1,3,4-Thiadiazoles and Imidazo[2,1-b][1,3,4]thiadiazoles.
Tryfon Zarganes-Tzitzikas,Constantinos G. Neochoritis,Julia Stephanidou-Stephanatou,Constantinos A. Tsoleridis,Gernot Buth,George E. Kostakis +5 more
TL;DR: In this paper, the 3-thione substituent was replaced by the 5-thion substituents, and the thiadiazoles became the only reaction products, formed in very good yield by using 2-equiv of azodicarboxylates.
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One-Pot Synthesis of Functionalized Spirobenzofuranones via MCR Involving 3-Cyanochromones.
Tryfon Zarganes-Tzitzikas,Michael A. Terzidis,Julia Stephanidou-Stephanatou,Constantinos A. Tsoleridis,George E. Kostakis +4 more
TL;DR: Treatment of 3-cyanochromones with isocyanides and acetylenecarboxylates allows a new and facile access to spirobenzofuranones of biological interest.