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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 40, 2010 - Issue 16
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Original Articles

Ionic Liquid–Mediated, One-Pot Synthesis for 4-Thiazolidinones

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Pages 2397-2401 | Received 20 May 2009, Published online: 26 Jul 2010

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Read on this site (7)

Nayana Pahade, Devendra Wagare, D. W. Shinde & Dinesh Lingampalle. (2023) Ionic Liquid Catalyzed One-Pot Synthesis of 5-(4-Substituted-Phenyl)-1,3,4-Thiadiazole-2-Amines. Polycyclic Aromatic Compounds 43:10, pages 8593-8598.
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Amol V. Sapkal, Jaysing M. Dinore, Ajeet A. Yelwande, Manoj P. Palve & Balaji R. Madje. (2023) Ultrasound Promoted One-Pot Multicomponent Synthesis of Highly Functionalized Tetrahydropyridine Derivatives. Polycyclic Aromatic Compounds 0:0, pages 1-11.
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Navjeet Kaur. (2019) Ionic liquid assisted synthesis of S-heterocycles. Phosphorus, Sulfur, and Silicon and the Related Elements 194:3, pages 165-185.
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Amarsinh R. Deshmukh, Sambhaji T. Dhumal, Laxman U. Nawale, Vijay M. Khedkar, Dhiman Sarkar & Ramrao A. Mane. (2019) Dicationic liquid mediated synthesis of tetrazoloquinolinyl methoxy phenyl 4-thiazolidinones and their antibacterial and antitubercular evaluation. Synthetic Communications 49:4, pages 587-601.
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Poonam Gautam, Deepika Gautam & R.P. Chaudhary. (2014) Regioselective synthesis of new 2,5,6-trisubstituted 5,6-dihydro-2H-pyrazolo[3,4-d]thiazoles from 5-dimethylaminoethylene-thaozolidin-4-thiones. Journal of Sulfur Chemistry 35:6, pages 628-640.
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Articles from other publishers (27)

Simranpreet K. Wahan, Pooja A. Chawla, Parvesh Singh, Rupesh Kumar & Gaurav Bhargava. (2023) A Facile, Mechanochemical, Solvent-, and Catalyst-Free Synthesis of Functionalized 4-Thiazolidinones. SynOpen 07:04, pages 615-618.
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Hadis Goudarzi, Davood Habibi & Arezo Monem. (2023) Application of a novel deep eutectic solvent as a capable and new catalyst for the synthesis of tetrahydropyridines and 1,3-thiazolidin-4-ones. Scientific Reports 13:1.
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Jonas da Silva Santos, Joel Jones Junior & Flavia Martins da Silva. (2023) Solvent-free MALI-MGRE Procedure for Synthesizing 1,4-thiazolidin-4- one MALI (Mercaptoacetic Acid Looking Imine) MGRE (Mechanical Grinding Reaction Equipment). Current Organic Synthesis 20:2, pages 258-266.
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Pragya Pali, Dhananjay Yadav, Gaurav Shukla & Maya Shankar Singh. (2021) Copper(II)-Catalyzed [3+2] Annulation of Thioamides with AIBN: Facile Access to Highly Functionalized Thiazolidin-4-ones. Synthesis 54:06, pages 1613-1620.
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Monish Arbaz Ansari, Dhananjay Yadav & Maya Shankar Singh. (2020) Rhodium(II)-Catalyzed Annulative Coupling of β-Ketothioamides with α-Diazo Compounds: Access to Highly Functionalized Thiazolidin-4-ones and Thiazolines. The Journal of Organic Chemistry 85:13, pages 8320-8329.
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Navjeet Kaur, Pranshu Bhardwaj, Meenu Devi, Yamini Verma, Neha Ahlawat & Pooja Grewal. (2019) Ionic Liquids for the Synthesis of Five-Membered N,N-, N,N,N- and N,N,N,NHeterocycles. Current Organic Chemistry 23:11, pages 1214-1238.
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Navjeet Kaur. (2019) Ionic Liquids: A Versatile Medium for the Synthesis of Six-membered Two Nitrogen- Containing Heterocycles. Current Organic Chemistry 23:1, pages 76-96.
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Subbiah SowmiahJosé M. S. S. Esperança, Luís P. N. Rebelo & Carlos A. M. Afonso. (2018) Pyridinium salts: from synthesis to reactivity and applications. Organic Chemistry Frontiers 5:3, pages 453-493.
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Dushyant V. Patel & Nirav R. Patel. 2018. Vicinal Diaryl Substituted Heterocycles. Vicinal Diaryl Substituted Heterocycles 245 276 .
Sadaf Mutahir, Muhammad Asim Khan, Islam Ullah Khan, Muhammad Yar, Muhammad Ashraf, Sidra Tariq, Ren-long Ye & Bao-jing Zhou. (2017) Organocatalyzed and mechanochemical solvent-free synthesis of novel and functionalized bis-biphenyl substituted thiazolidinones as potent tyrosinase inhibitors: SAR and molecular modeling studies. European Journal of Medicinal Chemistry 134, pages 406-414.
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Lalit D. Khillare, Manisha R. Bhosle, Amarsinh R. Deshmukh & Ramrao A. Mane. (2015) One-pot rapid synthesis of thiazole-substituted pyrazolyl-4-thiazolidinones mediated by diisopropylethylammonium acetate. Research on Chemical Intermediates 41:11, pages 8955-8964.
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Anshu Dandia, Ruby Singh, Jyoti Joshi & Shuchi Maheshwari. (2014) Green and chemoselective synthesis of pyrazolo[3,4-e][1,4]thiazepines and evaluation of their anti-infective activities. Research on Chemical Intermediates 41:7, pages 4213-4226.
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Lalit D. Khillare, Manisha R. Bhosle, Amarsinh R. Deshmukh & Ramrao A. Mane. (2014) Synthesis and anti-inflammatory evaluation of new pyrazoles bearing biodynamic thiazole and thiazolidinone scaffolds. Medicinal Chemistry Research 24:4, pages 1380-1386.
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Hellen G. Masteloto, Bruna B. Drawanz, Gabriele A. Berwaldt, Patricia D. Neuenfeldt, Geonir M. Siqueira & Wilson Cunico. (2014) 3,4-(Methylenedioxy)aniline as precursor to the synthesis of thiazolidin-4-ones. Monatshefte für Chemie - Chemical Monthly 146:2, pages 327-334.
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Girijesh Kumar Verma, Gaurav Shukla, Anugula Nagaraju, Abhijeet Srivastava & Maya Shankar Singh. (2014) DMAP-promoted cascade C–S/C–N bonds formation approach to 1,3-thiazolidin-4-ones via annulation of β-ketothioamides with α-halocarboxylic acids at room temperature. Tetrahedron 70:39, pages 6980-6984.
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Poovan Shanmugavelan, Murugan Sathishkumar, Sangaraiah Nagarajan, Raja Ranganathan & Alagusundaram Ponnuswamy. (2013) The First Solvent‐Free, Microwave‐Accelerated, Three‐Component Synthesis of Thiazolidin‐4‐ones via One‐Pot Tandem Staudinger/aza‐Wittig Reaction. Journal of Heterocyclic Chemistry 51:4, pages 1004-1011.
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Girijesh Kumar Verma, Gaurav Shukla, Anugula Nagaraju, Abhijeet Srivastava, Keshav Raghuvanshi & Maya Shankar Singh. (2014) DMAP-promoted domino annulation of β-ketothioamides with internal alkynes: a highly regioselective access to functionalized 1,3-thiazolidin-4-ones at room temperature. RSC Adv. 4:23, pages 11640-11647.
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Sophie Pelletier, Benjamin Pinson, Tomas Smejkal & Clemens Lamberth. (2013) A general synthesis of tetrahydropyrazolo[3,4-d]thiazoles. Tetrahedron 69:23, pages 4641-4651.
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Dinesh Kumar, Mukesh Sonawane, Brahmam Pujala, Varun K. Jain, Srikant Bhagat & Asit K. Chakraborti. (2013) Supported protic acid-catalyzed synthesis of 2,3-disubstituted thiazolidin-4-ones: enhancement of the catalytic potential of protic acid by adsorption on solid supports. Green Chemistry 15:10, pages 2872.
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Kothanahally S. Sharath Kumar, Toreshettahally R. Swaroop, Kachigere B. Harsha, Kereyagalahally H. Narasimhamurthy & Kanchugarakoppal S. Rangappa. (2012) T3P®-DMSO mediated one pot cascade protocol for the synthesis of 4-thiazolidinones from alcohols. Tetrahedron Letters 53:42, pages 5619-5623.
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Davinder Prasad & Mahendra Nath. (2012) Three‐Component Domino Reaction in PPG: An Easy Access to 4‐Thiazolidinone Derivatives. Journal of Heterocyclic Chemistry 49:3, pages 628-633.
Crossref
Manisha R. Bhosle, Jyotirling R. Mali, Aparna A. Mulay & Ramrao A. Mane. (2011) Polyethylene glycol mediated one‐pot three‐component synthesis of new 4‐thiazolidinones. Heteroatom Chemistry 23:2, pages 166-170.
Crossref
Asha B. Thomas, Rabindra K. Nanda, Lata P. Kothapalli & Avinash D. Deshpande. (2011) Synthesis and Antimicrobial Activity of N-[2-(aryl/substituted aryl)-4-oxo-1,3-thiazolidin-3-yl]pyridine-4-carboxamide. Journal of the Korean Chemical Society 55:6, pages 960-968.
Crossref
DHANAJI V JAWALE, UMESH R PRATAP, APARNA A MULAY, JYOTIRLING R MALI & RAMRAO A MANE. (2011) Synthesis of New dihydropyrimidinones catalysed by dicationic ionic liquid. Journal of Chemical Sciences 123:5, pages 645-655.
Crossref
Dhanaji V. Jawale, Umesh R. Pratap, Dinesh L. Lingampalle & Ramrao A. Mane. (2011) Dicationic Ionic Liquid Mediated Synthesis of 5‐Arylidine‐2,4‐thiazolidinediones. Chinese Journal of Chemistry 29:5, pages 942-946.
Crossref
Umesh R. Pratap, Dhanaji V. Jawale, Manisha R. Bhosle & Ramrao A. Mane. (2011) Saccharomyces cerevisiae catalyzed one-pot three component synthesis of 2,3-diaryl-4-thiazolidinones. Tetrahedron Letters 52:14, pages 1689-1691.
Crossref
Dinesh Lingampalle, Dhanaji Jawale, Rahul Waghmare & Ramrao Mane. (2010) ChemInform Abstract: Ionic Liquid‐Mediated, One‐Pot Synthesis for 4‐Thiazolidinones.. ChemInform 42:4.
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