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Phosphorus, Sulfur, and Silicon and the Related Elements Volume 180, 2005 - Issue 8
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Original Articles

Studies of Thiazolopyridines, Part 6: Synthesis and Antimicrobial Evaluation of Some Novel Thiazolo[3,2-a] Pyridine and Thiazolo[2′,3′:6,1]-pyrido[2,3-d]pyrimidine Derivatives

G. A. M. El-Hag Ali Department of Chemistry, Al-Azhar University, Nasr City, Cairo, Egypt
,
A. K. Khalil Department of Chemistry, Ain Shams University Cairo, Egypt
,
R. Q. Lamphon Department of Chemistry, King Abdel-Aziz University, Madine Munawarah, Saudia
&
A. A. El-Maghraby Department of Chemistry, Al-Azhar University, Nasr City, Cairo, Egypt
Pages 1909-1919 | Received 06 Jul 2004, Accepted 07 Sep 2004, Published online: 18 Aug 2006

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Himani Gupta, Rashmi Sharma & Anil Kumar. (2023) Multi-component syntheses based on β-oxodithioesters. Synthetic Communications 53:16, pages 1279-1304.
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Muhammad Shahid Nazir, Anam Nawaz, Sana Aslam, Matloob Ahmad, Ameer Fawad Zahoor & Noor ul Amin Mohsin. (2023) Synthetic strategies for thiazolopyridine derivatives. Synthetic Communications 53:7-8, pages 519-546.
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Y.A. Ammar, Y.A. Mohamed, G.A. M. El-Hagali, A. S. Abd El-Aal & M.S. A. El-Gaby. (2010) Some Cyclization Reactions with 2-Ethoxycarbonylmethylidene-4,5-Dihydro-4-Thiazolinone. Phosphorus, Sulfur, and Silicon and the Related Elements 185:7, pages 1386-1394.
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Articles from other publishers (19)

Hadiseh Rouzban, Mohammad Bayat & Hajar Hosseini. (2022) Efficient regioselective five-component synthesis of novel thiazolo[3,2-a]pyridine carbohydrazides and oxazolo[3,2-a]pyridine carbohydrazides. Molecular Diversity 27:2, pages 667-678.
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Firudin I. Guseinov, Vladislav M. Malinnikov, Kirill N. Lialin, Konstantin I. Kobrakov, Elena V. Shuvalova, Yulia V. Nelyubina, Bogdan I. Ugrak, Leonid M. Kustov & Kamran T. Mahmudov. (2022) Charge-assisted chalcogen bonding in 2-(4-substituted benzoyl)thiazolo[3,2-a]pyridin-4-ium bromides. Dyes and Pigments 197, pages 109898.
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Zohreh Sahhaf Razavi, Mohammad Bayat & Hajar Hosseini. (2020) Synthesis of highly functionalized thiazolo[3,2- a ]pyridine derivatives via a five-component cascade reaction based on nitroketene N , S -acetal . RSC Advances 10:52, pages 31039-31048.
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Mohammad Bayat, Fatemeh Safari, Shima Nasri & Fahimeh Sadat Hosseini. (2019) A chemoselective synthesis and biological evaluation of novel benzo[g]thiazolo[3,2-a]quinolone derivatives. Monatshefte für Chemie - Chemical Monthly 150:4, pages 703-710.
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Kavitha Kotthireddy, Srikrishna Devulapally, Pramod Kumar Dubey & Aparna Pasula. (2019) An Efficient One‐pot Three‐component Method for the Synthesis of 5‐Amino‐3‐(2‐oxo‐2 H ‐chromen‐3‐yl)‐7‐aryl‐7 H ‐thiazolo[3,2‐a]pyridine‐6,8‐dicarbonitriles . Journal of Heterocyclic Chemistry 56:3, pages 938-946.
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Shima Nasri, Fahimeh Sadat Hosseini & Mohammad Bayat. (2018) Solvent-controlled dehydration and diastereoselective formation of indenone-fused thiazolo[3,2-a]pyridines via a one-pot four-component reaction. Tetrahedron 74:33, pages 4409-4417.
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Galina A. Gazieva, Alexei N. Izmest’ev, Lada V. Anikina, Sergey A. Pukhov, Marina E. Meshchaneva, Dmitry V. Khakimov, Natalya G. Kolotyrkina & Angelina N. Kravchenko. (2018) The influence of substituents on the reactivity and cytotoxicity of imidazothiazolotriazinones. Molecular Diversity 22:3, pages 585-599.
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G. A. M. Elhagali, G. A. Elsayed, R. A. Eliswey & A. A. El-Sherif. (2018) Molecular modeling and cyclization reactions of 2-(4-oxothiazolidine-2-ylidene) acetonitrile. Journal of the Iranian Chemical Society 15:6, pages 1243-1254.
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Dhanasekar Elumalai, Ramachandran Gnanasekaran, Saraswathi Leelakrishnan, Gunavathy Nachimuthu, Tharanikkarasu Kannan, Thirumalai Perumal Paramasivam & Kamalraja Jayabal. (2018) InCl 3 ‐Assisted Eco‐Friendly Approach for N‐Fused 1,4‐Dihydropyridine Scaffolds via Ring Opening Michael Addition of Cyclic Nitroketene and Iminocoumarin: Synthesis and DFT Studies . ChemistrySelect 3:7, pages 2070-2079.
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Shimaa Abdel Halim & Ali Kh. Khalil. (2017) TD-DFT calculations, NBO analysis and electronic absorption spectra of some thiazolo[3,2-a]pyridine derivatives. Journal of Molecular Structure 1147, pages 651-667.
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Richa Gupta. (2016) Recent Advances in Chemistry of Condensed 4-Thiazolidinones. Journal of Heterocyclic Chemistry 53:6, pages 1687-1696.
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I. V. Dyachenko. (2015) New multicomponent synthesis of functionally substituted partially hydrogenated thiazolo[3,2-a]quinoline and thiazolo[3,2-a]pyridine. Russian Journal of Organic Chemistry 51:11, pages 1584-1586.
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Nagy M. Khalifa, Adel A.-H. Abdel-Rahman, Sherein I. Abd-Elmoez, Omar A. Fathalla & Amina A. Abd El-Gwaad. (2013) A convenient synthesis of some new fused pyridine and pyrimidine derivatives of antimicrobial profiles. Research on Chemical Intermediates 41:4, pages 2295-2305.
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Muthusamy Boominathan, Muthupandi Nagaraj, Chellaiah Maheshwaran, Shanmugam Muthusubramanian & Nattamai Bhuvanesh. (2014) One-Pot Green Synthesis of Thiazolo[3,2- a ]pyridine Derivatives via Tandem Cyclization in Aqueous Media . Journal of Heterocyclic Chemistry 51:1, pages 244-248.
Crossref
Hai-Liang Chen & Hong-Yun Guo. (2012) One-Pot Synthesis of Thiazolo[3,2-α]Pyridine Derivatives Catalysed by Ionic Liquids. Journal of Chemical Research 36:3, pages 162-165.
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Cevher Altug, Alan K. Burnett, Esra Caner, Yaşar Dürüst, Mark C. Elliott, Roger P.J. Glanville, Carol Guy & Andrew D. Westwell. (2011) An efficient one-pot multicomponent approach to 5-amino-7-aryl-8-nitrothiazolo[3,2-a]pyridines. Tetrahedron 67:49, pages 9522-9528.
Crossref
Feng Shi, Chunmei Li, Ming Xia, Kangjie Miao, Yanxia Zhao, Shujiang Tu, Weifa Zheng, Ge Zhang & Ning Ma. (2009) Green chemoselective synthesis of thiazolo[3,2-a]pyridine derivatives and evaluation of their antioxidant and cytotoxic activities. Bioorganic & Medicinal Chemistry Letters 19:19, pages 5565-5568.
Crossref
R.L. Riggs & D.M. Smith. 2008. Comprehensive Heterocyclic Chemistry III. Comprehensive Heterocyclic Chemistry III 857 973 .
G. A. M. El‐Hag Ali, A. K. Khalil, R. Q. Lamphon & A. A. El‐Maghraby. (2005) Studies of Thiazolopyridines. Part 6. Synthesis and Antimicrobial Evaluation of Some Novel Thiazolo[3,2‐a]pyridine and Thiazolo[2′,3′:6,1]pyrido[2,3‐d]pyrimidine Derivatives.. ChemInform 36:46.
Crossref

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