Reaction between thiocarbamidoalkyl naphthols and acetylenic esters: An interesting cyclocondensation reaction for the synthesis of new thiazolidin-4-one derivatives
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Chemistry
Link
http://link.springer.com/content/pdf/10.1007/s12039-015-0944-5.pdf
Reference22 articles.
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3. Soleimani E and Zainali M 2012 Synth. Commun. 42 1885
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5. Zare A, Yousofi T and Moosavi Zare A R 2012 RSC Adv. 2 7988
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1. Efficient Synthesis of Novel Thioureidobenzamido Alkyl Naphthols in Molten Tetrabutylammonium Bromide;Letters in Organic Chemistry;2019-10-02
2. Visible-Light-Promoted Three-Component Coupling Annulation: Synthesis of 2-Iminothiazolidin-4-ones via in Situ Formed Electron Donor–Acceptor Complexes;The Journal of Organic Chemistry;2019-03-07
3. Synthesis of novel amidoalkyl naphthol-based azo dyes and evaluation of their antimicrobial activities;Journal of the Iranian Chemical Society;2018-12-12
4. A novel tandem Betti/Ullmann oxidation reaction as an efficient route for synthesis of new oxazepine derivatives;Journal of Chemical Sciences;2017-07-25
5. ChemInform Abstract: Reaction Between Thiocarbamidoalkyl Naphthols and Acetylenic Esters: An Interesting Cyclocondensation Reaction for the Synthesis of New Thiazolidin-4-one Derivatives.;ChemInform;2016-03
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