167
Views
4
CrossRef citations to date
0
Altmetric
Research Articles

Fe3O4@NCs/Sb(V): As a Cellulose Based Nano-Catalyst for the Synthesis of 4H-Pyrimido[2,1-b]benzothiazoles

&
Pages 1013-1022 | Received 26 Feb 2020, Accepted 30 Apr 2020, Published online: 19 May 2020

References

  • Leila Zare Fekri, Mohammad Nikpassand, Sakineh Pourmirzajani, and Behnaz Aghazadeh, “Synthesis and Characterization of Aminoglucose Functionalized Silica-Coated NiFe2O4 Nanoparticles: A Heterogeneous, New and Magnetically Separable Catalyst for the Solvent-Free Synthesis of Pyrano[3,2-c]Chromen-5(4H)-Ones,” RSC Advances 8, no. 40 (2018): 22313–20.
  • Behnaz Aghazadeh, and Mohammad Nikpassand, “2-Aminoglucose as a Substrate for Synthesis of Magnetically Recoverable Nanocatalyst NiFe2O4@SiO2@Amino Glucose for the Green Synthesis of Novel Bis(1,2-Dihydro-4-Hydroxy-2-Oxoquinolin-3-yl)Methanes,” Carbohydrate Research 483 (2019): 107755.
  • Mohammad Nikpassand, “NiFe2O4@SiO2@Glucoseamine Nanoparticle Catalyzed Reaction of Azo-Linked Thiosalicylic Acid with CO2: Access to Azo-Linked Benzo[d] Oxathiine-2,4-Diones,” Dyes and Pigments 173 (2020): 107936.
  • Mohammad Nikpassand, Leila Fekri, Lia Karimian, and Mehdi Rassa, “Synthesis of Biscoumarin Derivatives Using Nanoparticle Fe3O4 as an Efficient Reusable Heterogeneous Catalyst in Aqueous Media and Their Antimicrobial Activity,” Current Organic Synthesis 12, no. 3 (2015): 358–62.
  • Leila Zare Fekri, Mohammad Nikpassand, Shahab Shariati, Behnaz Aghazadeh, Reza Zarkeshvari, and Nahid Norouz Pour, “Synthesis and Characterization of Aminoglucose Functionalized Silica‐Coated NiFe2O4 Nanoparticles: A Heterogeneous, New and Magnetically Separable Catalyst for the Solvent‐Free Synthesis of 2,4,5–Trisubstituted Imidazoles, Benzo[d]imidazoles, Benzo[d]oxazoles and Azo-Linked Benzo[d]Oxazoles,” Journal of Organometallic Chemistry 871 (2018): 60–73.
  • Mohammad Nikpassand, Leila Zare Fekri, and Sina Sanagou, “Green Synthesis of 2-Hydrazonyl-4-Phenylthiazoles Using KIT-6 Mesoporous Silica Coated Magnetite Nanoparticles,” Dyes and Pigments 136 (2017): 140–4.
  • Naeimeh Salehi, and Bi Bi Fatameh Mirjalili, “Synthesis of Highly Substituted Dihydro-2-Oxopyrroles Using Fe3O4@Nano-Cellulose–OPO3H as a Novel Bio-Based Magnetic Nanocatalyst,” RSC Advances 7, no. 48 (2017): 30303–9.
  • Sara Azad, and Bi Bi Fatameh Mirjalili, “Fe3O4@Nano-Cellulose/TiCl: A Bio-Based and Magnetically Recoverable Nano-Catalyst for the Synthesis of Pyrimido [2,1-b] Benzothiazole Derivatives,” RSC Advances 6, no. 99 (2016): 96928–34.
  • Yongliang Liu, “Chemical Composition and Characterization of Cotton Fibers,” Cotton Fiber: Physics, Chemistry and Biology (2018): 75–94.
  • Noor Rehman, Sultan Alam, Noor Ul Amin, Inamullah Mian, and Hidayat Ullah, “Ecofriendly Isolation of Cellulose from Eucalyptus Lenceolata: A Novel Approach,” International Journal of Polymer Science 2018 (2018): 1–7.
  • Albert Mihranyan, “Cellulose from Cladophorales Green Algae: From Environmental Problem to High‐Tech Composite Materials,” Journal of Applied Polymer Science 119, no. 4 (2011): 2449–60.
  • Gandhi Divyani, Kalal Priyanka, Prajapat Prakash, K. Agarwal Dinesh, and Agarwal Shikha, “Diversity Oriented Synthesis of 4H-Pyrimido[2,1-b]benzothiazole Derivatives via Biginellis Reaction: A Review,” Combinatorial Chemistry & High Throughput Screening 21, no. 4 (2018): 236–53.
  • Tilak Raj, Hemant Sharma, Mayank, Ajnesh Singh, Thammarat Aree, Navneet Kaur, Narinder Singh, and Doo Ok Jang, “Solvent-Less Mechanochemical Approach to the Synthesis of Pyrimidine Derivatives,” ACS Sustainable Chemistry & Engineering 5 (2017): 1468–75.
  • Agarwal Shikha, Kr Agarwal Dinesh, Gandhi Divyani, Goyal Kshamta, and Goyal Pradeep, “Multicomponent One-Pot Synthesis of Substituted 4H-Pyrimido [2,1-b] [1,3] Benzothiazole Curcumin Derivatives and Their Antimicrobial Evaluation,” Letters in Organic Chemistry 15, no. 10 (2018): 863–9.
  • Shikha Agarwal, Dinesh Kr Agarwal, Priyanka Kalal1, and Divyani Gandhi, “A comparative study: Greener vs conventional synthesis of 4H-pyrimido[2,1-b]benzothiazoles via Biginelli reaction,” AIP Conference Proceedings 1953, no. 08001 (2018). doi: https://doi.org/10.1063/1.5032807.
  • Goyal Kshamta, Agarwal Shikha, Kr Agarwal Dinesh, Gautam Naveen, and D. C. Gautam, “Synthesis, Spectral Characterization and Biological Evaluation of New Substituted 2H-Pyrimido[2,1-b]Benzothiazol-2-Ones,” Letters in Organic Chemistry 13, no. 10 (2017): 726–33.
  • Moustafa T. Gabr, Nadia S. El-Gohary, Eman R. El-Bendary, and Mohamed M. El-Kerdawy, “New Series of Benzothiazole and Pyrimido[2,1-b]Benzothiazole Derivatives: Synthesis, Antitumor Activity, EGFR Tyrosine Kinase Inhibitory Activity and Molecular Modeling Studies,” Medicinal Chemistry Research 24, no. 2 (2015): 860–78.
  • Vinaykumar Deshmukh, Ravi Prasad, Prafullakumar Kulkarni, and Sharad V. Kuberkar, “Design, Synthesis and Biological Activities of Novel 4H-Pyrimido[2,1-b][1,3]Benzothiazole Derivatives,” International Journal of ChemTech Research 3, no. 1 (2011): 136–42.
  • Leena B. Labhsetwar, Giridhar R. Shendarkar, and Sharad V. Kuberkar, “Synthesis and in Vitro Anticancer Activity of 8-Chloro-3-Cyano-4-Imino-2-Methylthio-4H-Pyrimido[2,1-b][1,3]Benzothiazole and Its 2-Substituted Derivatives,” Asian Journal of Pharmaceutical Research and Health Care 2, no. 3 (2010): 273–8.
  • Magde A. El-Sherbeny, “Synthesis of Certain Pyrimido[2,1-b]Benzo-Thiazole and Benzothiazolo[2,3-b]Quinazoline Derivatives for in Vitro Antitumor and Antiviral Activities,” Arzneimittelforschung 50, no. 9 (2011): 848–53.
  • Pramod K. Sahu, Praveen K. Sahu, Sushil K. Gupta, Duraipandian Thavaselvam, and Dau D. Agarwal, “Synthesis and Evaluation of Antimicrobial Activity of 4H-Pyrimido[2,1-b]Benzothiazole, Pyrazole and Benzylidene Derivatives of Curcumin,” European Journal of Medicinal Chemistry 54 (2012): 366–78.
  • Shikha Gupta, Neha Ajmera, Naveen Gautam, Rajni Sharma, and D. C. Gautam, “Novel Synthesis and Biological Activity Study of Pyrimido[2,1-b] Benzothiazoles,” Indian Journal of Chemistry 48B, no. 6 (2009): 853–7.
  • Pramod K. Sahu, Praveen K. Sahu, Jaggi Lal, Duraipandian Thavaselvam, and Dau D. Agarwal, “A Facile Green Synthesis and in Vitro Antimicrobial Activity 4H-Pyrimido[2,1-b][1,3]Benzothiazole Derivatives Using Aluminumtrichloride under Solvent-Free Conditions,” Medicinal Chemistry Research 21, no. 11 (2012): 3826–34.
  • Moulay H. Youssoufi, Pramod K. Sahu, Praveen K. Sahu, Dau D. Agarwal, Mushtaq Ahmad, Mouslim Messali, Siham Lahsasni, and Taibi Ben Hadda, “POM Analyses of Antimicrobial Activity of 4H-Pyrimido[2,1-b]Benzothiazole, Pyrazole, and Benzylidene Derivatives of Curcumin,” Medicinal Chemistry Research 24, no. 6 (2015): 2381–92.
  • Ruhi Ali, and Nadeem Siddiqui, “Biological Aspects of Emerging Benzothiazoles: A Short Review,” Journal of Chemistry 2013 (2013): 1–13.
  • Joseph P. Yevich, Davis L. Temple, Jr., R. R. Covington, Desmond Owens, Richard J. Seidehamel, and Kendrick W. Dungan, “Antiallergics: 3-(1H-Tetrazol-5-yl)-4H-Pyrimido[2,1-b]Benzothiazol-4-Ones,” Journal of Medicinal Chemistry 25, no. 7 (1982): 864–8.
  • Deepak Mene, and Mayura Kale, “Exploration of Different Methodologies for Synthesizing Biologically Important Benzothiazoles: An Overview,” Current Organic Synthesis 13, no. 1 (2015): 41–57.
  • R. Yadav Mukesh, K. Deshmukh Vinayak, and R. Chaudhari Sanjay, “Microwave Assisted Synthesis and Anticancer Activity of Substituted Pyrimido[2,1-b][1,3]benzothiazole Derivatives,” International Journal of Pharmaceutical Sciences Review and Research 22, no. 1 (2013): 41–7.
  • Ahmad Shaabani, Abbas Rahmati, and Soheila Naderi, “A Novel One-Pot Three-Component Reaction: Synthesis of Triheterocyclic 4H-Pyrimido[2,1-b]Benzazoles Ring Systems,” Bioorganic & Medicinal Chemistry Letters 15, no. 24 (2005): 5553–7.
  • Amol B. Atar, Yong Seok Jeong, and Yeon Tae Jeong, “Iron Fluoride: The Most Efficient Catalyst for One-Pot Synthesis of 4H-Pyrimido[2,1-b]Benzothiazoles under Solvent-Free Conditions,” Tetrahedron 70, no. 34 (2014): 5207–13.
  • Sayujiata R. Vaidya, and Jaishri Chamergore, “Thiamine Hydrochloride (VB1) as an Efficient Catalyst for the Synthesis of 4H-Pyrimido [2,1-b] Benzothiazole Derivatives,” Chemistry & Biology Interface 6, no. 1 (2016): 47–51.
  • Lingaiah Nagarapu, Hanmant K. Gaikwad, Jyothsna Devi Palem, Ramineni Venkatesh, Rajashaker Bantu, and B. Sridhar, “Convenient Approach for the One-Pot, Three-Component Synthesis of Triheterocyclic 4H-Pyrimido[2,1-b]Benzothiazole Derivatives Using TBAHS,” Synthetic Communications 43, no. 1 (2013): 93–104.
  • Pramod Kumar Sahu, Praveen Kumar Sahu, and Dau Dayal Agarwal, “Efficient and Facile Synthesis of Heterocycles and Their Mechanistic Consideration Using Kaolin,” RSC Advances 3, no. 25 (2013): 9854.
  • Pramod Kumar Sahu, Praveen Kumar Sahu, Yogesh Sharma, and Dau Dayal Agarwal, “Synthesis and Mechanistic Study of Triheterocyclic 4H‐Pyrimido[2,1‐b]Benzothiazole Derivatives, One‐Pot Three‐Component Reaction under Solvent‐Free Conditions,” Journal of Heterocyclic Chemistry 51, no. 4 (2014): 1193–8.
  • Seyede Azita Fazeli-Attar, and Bi Bi Fatemeh Mirjalili, “Nano-Fe3O4@SiO2–TiCl3 as a Novel Nano-Magnetic Catalyst for the Synthesis of 4H-Pyrimido[2,1-b]Benzothiazoles,” Research on Chemical Intermediates 44, no. 10 (2018): 6419–30.
  • Bi Bi Fatemeh Mirjalili, and Fatemeh Aref, “Nano-Cellulose/BF3/Fe3O4: A Magnetic Bio-Based Nano-Catalyst for the Synthesis of Pyrimido[2,1-b]Benzothiazoles under Solvent-Free Conditions,” Research on Chemical Intermediates 44, no. 7 (2018): 4519–31.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.