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RESEARCH ARTICLE

Synthesis of some new fused thiopyrano[2,3-d]thiazoles and their derivatives

Pages 275-284 | Received 24 Nov 2006, Published online: 16 May 2007

Keep up to date with the latest research on this topic with citation updates for this article.

Read on this site (6)

Nataliya Zelisko, Olexandr Karpenko, Volodymyr Muzychenko, Andrzej Gzella & Roman Lesyk. (2021) Citraconic acid and its anhydride-based hetero-Diels–Alder reactions in the synthesis of new thiopyrano[2,3-d][1,3]thiazole derivatives. Synthetic Communications 51:6, pages 964-970.
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Nadia Hanafy Metwally, Mohamed Ahmed Badawy & Doha Samir Okpy. (2018) Green synthesis of some new thiopyrano[2,3-d][1,3]thiazoles using lemon juice and their antibacterial activity. Synthetic Communications 48:19, pages 2496-2509.
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Nadia Hanafy Metwally & Ibrahim Adel El-Doseky. (2015) Facile Synthesis of Some New Pyrazole-Based 2-Thioxo-4-thiazolidinone. Synthetic Communications 45:23, pages 2683-2690.
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Mohamed Ahmed Badawy, Nadia Hanafy Metwally & Doha Samir Okpy. (2015) Synthesis of some new 5-substituted-3-phenyl-4-thioxo-2-thiazolidinones and their fused thiopyrano[2,3-d]thiazole derivatives. Journal of Sulfur Chemistry 36:5, pages 511-525.
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Dmytro Atamanyuk, Borys Zimenkovsky & Roman Lesyk. (2008) Synthesis and anticancer activity of novel thiopyrano[2,3-d]thiazole-based compounds containing norbornane moiety. Journal of Sulfur Chemistry 29:2, pages 151-162.
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Articles from other publishers (10)

Andrii Lozynskyi, Ihor Yushyn, Yulia Shepeta, Olexandr Karpenko, Andrzej K. Gzella & Roman Lesyk. (2022) Synthesis and structure elucidation of thiopyrano[2,3-d]thiazole-6-carbonitriles as adducts of Michael reaction. Journal of Molecular Structure 1256, pages 132574.
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Andrii Lozynskyi, Andriy Karkhut, Svyatoslav Polovkovych, Olexandr Karpenko, Serhii Holota, Andrzej K. Gzella & Roman Lesyk. (2022) 3-Phenylpropanal and citral in the multicomponent synthesis of novel thiopyrano[2,3-d]thiazoles. Results in Chemistry 4, pages 100464.
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Anna Kryshchyshyn, Olexandra Roman, Andrii Lozynskyi & Roman Lesyk. (2018) Thiopyrano[2,3-d]Thiazoles as New Efficient Scaffolds in Medicinal Chemistry. Scientia Pharmaceutica 86:2, pages 26.
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Danylo Kaminskyy, Anna Kryshchyshyn & Roman Lesyk. (2017) 5-Ene-4-thiazolidinones – An efficient tool in medicinal chemistry. European Journal of Medicinal Chemistry 140, pages 542-594.
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I. R. Siddiqui, Arjita Srivastava, Shayna Shamim, Anjali Srivastava, Shireen & Malik A. Waseem. (2016) An Efficient One-Pot Regioselective Approach Towards the Synthesis of Thiopyrano[2,3- d ]thiazole-2-thiones Catalyzed by Basic Ionic Liquid under Microwave Irradiation . Journal of Heterocyclic Chemistry 53:3, pages 849-858.
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Nataliya Zelisko, Dmytro Atamanyuk, Yuri Ostapiuk, Andriy Bryhas, Vasyl Matiychuk, Andrzej Gzella & Roman Lesyk. (2015) Synthesis of fused thiopyrano[2,3-d][1,3]thiazoles via hetero-Diels–Alder reaction related tandem and domino processes. Tetrahedron 71:50, pages 9501-9508.
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Nadia Hanafy Metwally, Mohamed Ahmed Badawy & Doha Samir Okpy. (2015) Synthesis and Anticancer Activity of Some New Thiopyrano[2,3-<i>d</i>]thiazoles Incorporating Pyrazole Moiety. CHEMICAL & PHARMACEUTICAL BULLETIN Chemical and Pharmaceutical Bulletin 63:7, pages 495-503.
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Nataliya Zelisko, Dmytro Atamanyuk, Olexandr Vasylenko, Andriy Bryhas, Vasyl Matiychuk, Andrzej Gzella & Roman Lesyk. (2014) Crotonic, cynnamic, and propiolic acids motifs in the synthesis of thiopyrano[2,3-d][1,3]thiazoles via hetero-Diels–Alder reaction and related tandem processes. Tetrahedron 70:3, pages 720-729.
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Venkata Ramana Sirivolu, Sanjeev Kumar V. Vernekar, Christophe Marchand, Alena Naumova, Adel Chergui, Amelie Renaud, Andrew G. Stephen, Feng Chen, Yuk Y. Sham, Yves Pommier & Zhengqiang Wang. (2012) 5-Arylidenethioxothiazolidinones as Inhibitors of Tyrosyl–DNA Phosphodiesterase I. Journal of Medicinal Chemistry 55:20, pages 8671-8684.
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Vasyl S. Matiychuk, Roman B. Lesyk, Mykola D. Obushak, Andrzej Gzella, Dmytro V. Atamanyuk, Yuri V. Ostapiuk & Anna P. Kryshchyshyn. (2008) A new domino-Knoevenagel–hetero-Diels–Alder reaction. Tetrahedron Letters 49:31, pages 4648-4651.
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