A convenient synthesis of thiazol-2(3H)-one skeletons from a reaction involving terminal alkynes, elemental sulfur, and isocyanates
Author:
Affiliation:
1. Faculty of Science, Department of Chemistry, University of Sistan and Baluchestan, Zahedan, Iran
2. Faculty of Science, Department of Chemistry, University of Zabol, Zabol, Iran
Publisher
Informa UK Limited
Subject
General Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/17415993.2019.1703987
Reference40 articles.
1. Synthesis of Functionalized 1,2-Dihydroisoquinolines via Multicomponent One-Pot Reaction of 2-Alkynylbenzaldehyde, Amine, Zinc, and Allylic Bromide or Benzyl Bromide
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3. Copper-Catalyzed Domino Addition, Hydroamination, and Cyclization: A Multicomponent Approach to Spiro Oxazolidinone Derivatives
4. Copper-Catalyzed Synthesis of Medium- and Large-Sized Nitrogen Heterocycles via N-Arylation of Phosphoramidates and Carbamates
5. Copper-Catalyzed C–H Functionalization Reactions: Efficient Synthesis of Heterocycles
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2. Preparation of 4-Arylthiazol-2(3H)-ones and the Three-Component Synthesis of Multidentate 5,5′-Methylenebis[4-arylthiazol-2(3H)-one] Ligands;Synthesis;2022-08-25
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5. Organo-catalytic synthesis of oxathians from isocyanides, isothiocyanates, and oxiranes;Journal of Sulfur Chemistry;2020-07-27
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