This submission belongs to the session a. General Organic Synthesis of the event The 18th International Electronic Conference on Synthetic Organic Chemistry
Published date
31 Oct, 2014
Citation
Richard Kammel, Synthesis of Substitued 5-(2-Hydroxyphenyl)-1,3-Thiazol-4-Oles AS pH Switchable Fluorophores, in Proceedings of The 18th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2014, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-18-a009
Share
Email
Facebook
Twitter
LinkedIn
Synthesis of Substitued 5-(2-Hydroxyphenyl)-1,3-Thiazol-4-Oles AS pH Switchable Fluorophores
Richard Kammel 1
1. Institute of Organic Chemistry and Technology Faculty of Chemical Technology University of Pardubice Studentská 573 532 10 PARDUBICE Czech Republic
Abstract
Present work is a continuation of our previous research done in the field of transformation reaction of isothiuronium salts derived from various lactones and lactames giving substituted 2-iminothiazolidin-4-ones or 2-aminothiazolin-4-ones. These compounds are known e.g. for their significant biological activity but they do not possess any fluorescence behaviour. On the other hand some substituted 1,3-thiazol-4-oles are good fluorophores in solutions and sometimes also in solid state. It is also known that the presence of some ionizable groups (OH, NH2 etc.) can significantly affect the shift of their UV absorption/fluorescence band. Therefore we have prepared a new set of substituted 5-(2-hydroxyphenyl)-1,3-thiazol-4-oles and studied their spectral properties under various conditions.
Keywords
Thioamide
1,3-thiazol-4-ole
fluorophore
transformation
3-bromocoumaran-2-one
Manuscript
ECSOC18.pdf
Poster
ECSOC18 presentation.pdf
Anti-Inflammatory Activity of Extracts of Leaves of Hygrophila Spinosa T. Anders in Chronic Animal Models of Inflammation
Synthesis of Pyrazole-Derived Dithioethers Using in situ Generation of Dithiolate-Ions