World Scientific News
EISSN 2392-2192
  • Login
  • Home
  • About
    • About Us
    • Editorial Board
    • Guide for Authors
    • Abstracting & Indexing
    • Instruction for Authors
    • Submit your Article
  • View Articles
    • 2026
    • 2025
    • 2024
    • 2023
    • 2022
    • 2021
    • 2020
    • 2019
    • 2018
    • 2017
    • 2016
    • 2015
    • 2014
    • 2013
  • Careers
  • News
No Result
View All Result
SUBMIT ARTICLE
Register
  • Home
  • About
    • About Us
    • Editorial Board
    • Guide for Authors
    • Abstracting & Indexing
    • Instruction for Authors
    • Submit your Article
  • View Articles
    • 2026
    • 2025
    • 2024
    • 2023
    • 2022
    • 2021
    • 2020
    • 2019
    • 2018
    • 2017
    • 2016
    • 2015
    • 2014
    • 2013
  • Careers
  • News
No Result
View All Result
World Scientific News
No Result
View All Result
Home 2024

Review on Cavintands Molecules: Calix[4] arene and Resorcin[4]arene

Authors: Juhi B. Upadhyay, Hitesh M. Parekh, WSN 195 (2024) 118-157

2024-08-14
Reading Time: 31 mins read
0

ABSTRACT

From last ten years extensive research on supramolecular chemistry has been carried upon, specifically on calixarenes, resorcinarenes and its cavitands due to its wide industrial applications. Researchers has developed, different types of novel supramolecular moiety using various traditional synthesis process by modifying certain reaction condition that may help to develop new character contain supramolecule. In this review we summarized different types of reactions like acid-amide reaction, esterification, Schiff base, chalcone, formylation etc. Development of new potential compounds by derivation of calix[4]arene and resorsine[4] arene on their upper rim or lower rim which shown liquid crystal materials, biological activity, drug delivery host-guest system, optical chemo sensor, catalysis and many other applications. Therefore, researchers line of attack on the green synthesis way, microwave irradiation and modified classical methods for synthesis. All the synthesized macromolecules prepared by different reactions and are very useful to develop a new supramolecular generation and it has create many application in the future.

REFERENCES

1. Lehn, J. M.; Supramolecular chemistry-scope and perspectives molecules, supermolecules and molecular devices. Angew. Chem. Int. Ed. 1988, 27, 89. https://doi.org/10.1002/anie.198800891

2. Supramol Chem, 2nd ed., J. W. Steed; J. L. Atwood; P. A. Gale; John Wiley and Sons: New York, 2012.

3. Lehn, J.; From supramolecular chemistry towards constitutional dynamic chemistry and adaptive chemistry. Chem Soc Rev. 2007, 106, 151. https://doi.org/10.1039/B616752G

4. Boinski, T.; Cieszkowski A; Szumna A.  Hybrid [n]Arenes through Thermodynamically Driven Macrocyclization Reactions. J. Org. Chem. 2015, 3488. https://doi.org/10.1021/acs.joc.5b00099

ADVERTISEMENT

5. Taylor & francis group. Synergy in supramolecular chemistry, 1st ed.; N. Tatsuya; Boca Raton: CRC Press, 2014.

6. Core Concepts in Supramolecular Chemistry and Nanochemistry, 1st ed.; J. W. Steed; D. R. Turner; K. J. Wallace; John Wiely & sons Ltd: John Wiley & Sons: West Sussex, England, 2007.

7. Monograph in Supramolecular Chemistry, C. D. Gutsche; J. F. Stoddart; The Royal Society of Chemistry: Cambridge, 1989.

8. Jozsef, S.; Introduction and General Overview of Cyclodextrin Chemistry. Chem. Rev. 1998, 98, 1743. https://doi.org/10.1021/cr970022c

9. Calixarenes for Separations, C. D. Gutsche; J. F. Stoddart; ACS Symposium Series: Washington, DC, 1989.

10. Hooley, R. J.; Rebek, J. Chemistry and Catalysis in Functional Cavitands. ACS Chem. Biol. 2009, 16, 255. https://doi.org/10.1016/j.chembiol.2008.09.015

11. Far, A. R.; Shivanyuk, A.; Rebek, J. Water-Stabilized Cavitands. J. Am. Chem. Soc. 2002, 124, 4.

12. Melegari, M.; Suman, M.; Pirondini, L.; Moiani, D. Supramolecular Sensing with Phosphonate Cavitands. Chem. Eur. J. 2008, 14, 5772. https://doi.org/10.1002/chem.200800327

13. Gibb, B., Kim, S. K., Ogoshi, T., Gibb, B. C. , Murray, J., Kim, K. The aqueous supramolecular chemistry of cucurbit[n]urils, pillar[n]arenes and deep-cavity cavitands. Chem Soc Rev. 2017, 9, 2479. https://doi.org/10.1039/C7CS00095B

14. Rudkevich, D. M.; Rebek, J.; Scripps, T.; Torrey, N.; Road, P.; Jolla, L. Self-Folding Cavitands, J. Am. Chem. Soc. 1998, 120, 12216. https://doi.org/10.1021/ja982970g

15. Rudkevich, D. M., Rebek, J., Deepening Cavitands. EurJOC. 1999, 120, 1991. https://doi.org/10.1002/(SICI)1099-0690(199909)1999:9%3C1991::AID-EJOC1991%3E3.0.CO;2-5

16. Blackwell, J. M., Foster, K. L., Beck, V. H., Piers, W. E. B(C6F5)3-Catalyzed Silation of Alcohols: A Mild, General Method for Synthesis of Silyl Ethers. J. Org. Chem. 1999, 64, 2577. https://doi.org/10.1021/jo9903003

17. Brook, A. G.; Nyburg, S. C.; Reynolds, W. F.; Poon, Y. C.; Chang, Y.; Lee, J. Silicon-29 NMR studies of relatively stable silaethylenes. J. Am. Chem. Soc. 1979, 101, 6752. https://doi.org/10.1021/ja00516a047

18. Synthesis of bowlic liquid crystals containing acyclotriveratrylene core, Vo, L. P.; San Jose State University, USA, 1997, 1611. https://doi.org/10.31979/etd.v8nw-gfun

19. Mcmurry, J. E., Christopher, J. Synthesis and conformation of unsubstituted calix[4]arene. Tetrahedron Lett. 1991, 32, 5655. https://doi.org/10.1016/S0040-4039(00)93521-4

20. Cram, D. J., Cram, J. M. Cyclophane chemistry: bent and battered benzene rings. Acc. Chem. Res. 1970, 4, 204. https://doi.org/10.1021/ar50042a003

21. Mezo, A.R., Sherman, J. C. Water-Soluble Cavitands:  Synthesis of Methylene-Bridged Resorcin[4]arenes Containing Hydroxyls and Phosphates at Their Feet and Bromomethyls and Thiomethyls at Their Rims, Journal of Organic Chemistry. 1998, 63, (20), 6824. https://doi.org/10.1021/jo980305k

22. Naumann, C., Roma, E., Peinador, C., Ren, T., Patrick, B. O., Kaifer, A. E., Sherman, J. C. Expanding Cavitand Chemistry: The Preparation and Characterization of [n]Cavitands with n≥4, Chem. Eur. J. 2001, 7, 1637. https://doi.org/10.1002/1521-3765(20010417)

23. Irwin, J. L., Sherburn, M.S. Practical Synthesis of Selectively Functionalized Cavitands. J. Org. Chem. 2000, 65, 602. https://doi.org/10.1021/jo991185z

24. Niederl, J. B., Vogel, H. J., Aldehyde—Resorcinol Condensations. J. Am. Chem. Soc. 1940, 62, 2512. https://doi.org/10.1021/ja01866a067

25. Bourgeois, J., Stoeckli-evans, H. Synthesis of New Resorcinarenes Under Alkaline Conditions. Helv. Chim. Acta. 2007, 88, 2722. https://doi.org/10.1002/hlca.200590211

26. Archives of Environmental Protection, Iwanek, W. A., Wzorek, A; Bentham Science- International Publisher of Journals, 398, 2009.

27. Düker, M. H., Gómez, R., Vande, C. M. L., Azov, V. A. Upper rim tetrathiafulvalene-bridged calix[4]arenes. Tetrahedron Lett. 2011, 52, 2881. https://doi.org/10.1016/j.tetlet.2011.03.140

28. Hauke, F., Myles, A. J., Rebek, J. Lower rim mono-functionalization of resorcinarenes. ChemComm. 2005, 33, 4164. https://doi.org/10.1039/B506048F.

29. Miao, S., Adams, R. D., Guo, D., Zhang, Q. Structural conformers of symmetry substituted resorcin[4]arenes. J. Mol. Struct. 2003, 659, 119. https://doi.org/10.1016/j.molstruc.2003.08.004

30. Perry, J. J. B., Kilburn, J. D. For a review of synthetic developments in host-guest chemistry. Contemp. Org. Synth., 1997, 4, 61. https://doi.org/10.1039/CO9970400061

31. Hogberg, A. S. Two stereoisomeric macrocyclic resorcinol-acetaldehyde condensation products. J. Org. Chem. 1980, 45, 4498. https://doi.org/10.1021/jo01310a046

32. Cay, S., Sayin, S., Engin, M. S., Eymur, S. Preparation and Characterization of Calix[4]aren-immobilized Magnetic Microcapsule and Its Application in Heavy Metal Removal, Polycyclic Aromatic Compounds., 2017, 40, 116. https://doi.org/10.1080/10406638.2017.1363063

33. Kundrat, O., Cisarova, I., Bo, S., Pojarova, M., Lhotak, P. Uncommon Regioselectivity in Thiacalix[4]arene Formylation. J. Org. Chem. 2009, 5, 4775. https://doi.org/10.1021/jo9005574

34. Chawla, H. M., Pant, N., Srivastava, B. Regioselective ipso formylation of p-tert-butylcalix[4]arene. Tetrahedron Lett. 2005, 46, 7259. https://doi.org/10.1016/j.tetlet.2005.08.041

35. Chawla, H. M., Santra, A. Convenient One Pot Procedure for Synthesis of Formylated Calix[n]arenes. Synth. Commun. 2006, 31, 17. https://doi.org/10.1081/SCC-100105385

36. Kumar, S., Chawla, H. M., Varadarajan, R. A single step preparation of p-sulphonated calixarenes. Indian J. Chem. 2003, 42, 2863.

37. Lukasek, J., Böhm, S., Dvořáková, H., Eigner, V., Lhoták, P. Regioselective Halogenation of Thiacalix[4]arenes in the Cone and 1,3-Alternate Conformations. Org. Lett. 2014, 16, 5100. https://doi.org/10.1021/ol5024536

38. Hudecek, O., Budka, J., Eigner, V., Lhot, P. Recognition of chiral anions using calix[4]arene-based ureido receptor in the 1,3-alternate conformation. Tetrahedron Lett. 2012, 68, 4187. https://doi.org/10.1016/j.tet.2013.11.030

39. Kundrat, O., Kroupa, J., Bohm, S., Eigner, V., Lhotak, P. Meta Nitration of Thiacalixarenes. J. Org. Chem. 2010, 75, 8372. https://doi.org/10.1021/jo1013492

40. Barrett, E. S., Irwin, J. L., Edwards, A. J., Sherburn, M. S. Superbowl Container Molecules. J. Am. Chem., 2006, 126, 16747. https://doi.org/10.1021/ja044405l

41. Karami, B., Khodabakhshi, S., Hashemi, F. Synthesis of a novel class of benzofurans via a three-component, regiospecific intramolecular heterocylization reaction. Tetrahedron Lett. 2013, 54, 3583. https://doi.org/10.1016/j.tetlet.2013.03.124

42. Kamaei, V., Karami, B. Silica-supported molybdic acid: preparation, characterization, and its catalytic application in synthesis of pyranocoumarins. Polycycl Aromat Compd. 2015, 34, 37.

43. Karami, B., Khodabakshi, S. Synthesis of a novel class of benzofurans via a three-component, regiospecific intramolecular heterocylization reaction. Polycycl Aromat Compd. 2013, 31, 7. https://doi.org/10.1016/j.tetlet.2013.03.124

44. Khodabakhshi, S., Karami, B. A rapid and eco-friendly synthesis of novel and known benzopyrazines using silica tungstic acid (STA) as a new and recyclable catalyst. Catal. Sci. Technol. 2012, 2, 1940. https://doi.org/10.1039/C2CY20227A

45. Karami, B., Ghashghaee, V., Khodabakhshi, S. Novel silica tungstic acid (STA): Preparation, characterization and its first catalytic application in synthesis of new benzimidazoles. Catal. Commun. 2012, 20, 71. https://doi.org/10.1016/j.catcom.2012.01.012

46. Aoyama, Y., Tanaka, Y., Toi, H., Ogoshi, H. 2. Molecular recognition of amino acids: two-point fixation of amino acids with bifunctional metalloporphyrin receptors. J. Am. Chem. Soc. 1988, 110, 634. https://doi.org/10.1021/ja00220a078

47. Timmerman, P., Verboom, W., Reinhoudt, D. N. Resorcinarenes. Tetrahedron Lett. 1996, 52, 2663. https://doi.org/10.1016/0040-4020(95)00984-1

48. Cram, D. J., Karbach, S., Kim, H., Knobler, C. B., Maverick, E. F., Ericson, J. L., Helgeson, R. C. Cavitands as open molecular vessels form solvates J. Am. Chem. Soc. 1988, 110, 2229. https://doi.org/10.1021/ja00215a037

49. Bonsignore, S., Cometti, G., Dalcanale, E., Du Vosel, A. New columnar liquid crystals Correlation between molecular structure and mesomorphic behaviour. Liq. Cryst. 1990, 8, 639. https://doi.org/10.1080/02678299008047377

50. Barrett, A. G. M., Braddock, D. C., Henschke, J. P., Walker, E. R. Ytterbium(III) triflate-catalysed preparation of calix[4]resorcinarenes: Lewis assisted Brønsted acidity. J. Chem. Soc. 1999, 1, 873. https://doi.org/10.1039/A809919G

51. Peterson, K. E., Smith, R. C., Mohan, R. S. Bismuth compounds in organic synthesis, Synthesis of resorcinarenes using bismuth triflate. Tetrahedron Lett. 2003, 44, 7723. https://doi.org/10.1016/j.tetlet.2003.08.093

52. Hedidi, M., Hamdi, S. M., Mazari, T., Boutemeur, B., Rabia, C. Microwave-assisted synthesis of calix [4] resorcinarenes. Tetrahedron Lett. 2006, 62, 5652. https://doi.org/10.1016/j.tet.2006.03.095

53. Kudo, H., Shigematsu, K., Mitani, K., Nishikubo, T. One-pot synthesis of a novel ladder polymer of calixarene via condensation reaction of resorcinol and alkanedial based on dynamic covalent chemistry. Macromolecules. 2008, 41, 2030. https://doi.org/10.1021/ma7019573

54. Mobinikhaledi, A., Kalhor, M., Ghorbani, A. R., Fatinejad, H. Chem. Asian J. 2010, 22, 1103.

55. Liu, K., Chen, S.L., Xiao, S.W., Zhang, X.L., Ba, D.C., Wang, D.Y., Du, G.Y. Ba, Y.S. Molecular simulation of protein transport controlled by pressure-driven flow in silica nanofluidic channels. Bulg. Chem. Commun. 2015, 47, 552.

56. Yashiro, A., Onodera, K., Li, C., Suzuki, Y., Katagiri, H. Supramol Chem. 2014, 26, 48. https://doi.org/10.1080/10610278.2013.822969

57. Konishi, H., Iwasaki, Y., Synth Commun. 1995, 6, 612.

58. Karami, B., Khodabakhshi, S., Safikhani, N., Arami, A. A green and highly efficient solvent-free synthesis of novel calicx [4] resorcinarene derivatives using tungstate sulfuric acid. Bull Korean Chem Soc. 2012, 33, 2. http://dx.doi.org/10.5012/bkcs.2012.33.1.123

59. Ngurah, B. I. G. M., Anwar, C. Synthesis of Benzoyl C-Phenylcalix [4] Resorcinaryl Octaacetate and Cinnamoyl C-Phenylcalix [4] arene for UV Absorbers. Indones. J. Chem. 2014, 14, 160. http://dx.doi.org/10.22146/ijc.21253

60. Darvish, F., Khazraee, S. Molecular iodine: An efficient and environment-friendly catalyst for the synthesis of calix[4]resorcinarenes. C. R. Acad. Sci. 2014, 17, 890. https://doi.org/10.1016/j.crci.2013.10.017

61. Knyazeva, I. R., Matveeva, V. I., Syakaev, V. V, Gabidullin, B. M., Gubaidullin, A. T., Gruner, M., Habicher, W. D., Burilov, A. R., Pudovik, M. A. Thiophosphorylated derivatives of meta-and ortho-hydroxybenzaldehydes in one-step syntheses of novel calix [4] resorcinols. Tetrahedron Lett. 2014, 55, 7209. https://doi.org/10.1016/j.tetlet.2014.11.019

62. McIldowie, M. J., Mocerino, M., Skelton, B. W., White, A. H. Facile Lewis Acid Catalyzed Synthesis of C4 Symmetric Resorcinarenes. Org. Lett. 2000, 2, 3869. https://doi.org/10.1021/ol006608u

63. Yasmin, L., Coyle, T., Stubbs, K. A., Raston, C. L. Stereospecific synthesis of resorcin [4] arenes and pyrogallol [4] arenes in dynamic thin films. ChemComm. 2013, 49, 10932. https://doi.org/10.1039/C3CC45176C.

64. Xu, M., Huo, F., Yin, C. A supramolecular sensor system to detect amino acids with different carboxyl groups. Sens. Actuators B Chem. 2017, 240, 1245. https://doi.org/10.1016/j.snb.2016.09.105

65. Oliveira, C. B. S., Meurer, Y. S. R., Oliveira, M. G., Medeiros, W. M. T. Q., Silva, Brito, A. C. F., Pontes, D. D. L., Andrade-neto, V. F. Comparative Study on the Antioxidant and Anti-Toxoplasma Activities of Vanillin and Its Resorcinarene Derivative. Molecules. 2014, 19, 5898. https://doi.org/10.3390/molecules19055898

66. Abosadiya, H. M., Hasbullah, S. A., Mackeen, M. M., Low, S. C., Ibrahim, N., Koketsu, M., Yamin, B. M. Synthesis, Characterization, X-ray Structure and Biological Activities of C-5-Bromo-2-hydroxyphenylcalix [4]-2-methyl resorcinarene. Molecules. 2013, 18, 13369. https://www.mdpi.com/1420-3049/18/11/13369#

67. Szumna, A., Wierzbicki, M., Iwanek, W., Stefa, K. Solvent-free synthesis and structure of 2-naphthol derivatives of resorcinarenes. Tetrahedron Lett. 2015, 71, 2222. http://www.sciencedirect.com/science/article/pii/S004040201500277X

68. Konishi, H., Sakakibara, H., Kobayashi, K., Morikawa, O. Synthesis of the parent resorcin [4] arene. J. Chem. Soc. 1999, 1, 2583. https://doi.org/10.1039/A905613K

69. Pashirova, T. N., Gibadullina, E. M., Burilov, A. R., Kashapov, R. R., Zhiltsova, E. P., Syakaev, V. V., Habicher, W. D., Latypov, S. K., Konovalov, A. I. Amphiphilic O-functionalized calix [4] resocinarenes with tunable structural behavior. RSC Adv. 2014, 4, 9912. https://doi.org/10.1039/C3RA46146G

70. Mulatier, J., Martinez, A., Dutasta, J. Investigating Host–Guest Complexes in the Catalytic Synthesis of Cyclic Carbonates from Styrene Oxide and CO2. ACS Catal. 2015, 150, 6748. https://doi.org/10.1021/acscatal.5b01545

71. Maslennikova, V. I., Burikhina, A. V., Vasyanina, L. K., Nifant, E. E. Amination of calix[4]resorcinarenes. First synthesis of calix[4]phenylenediamines. Russ. J. Gen. Chem. 2010, 80, 548. https://doi.org/10.1134/S1070363210030333

72. Pansuriya, P. B., Friedrich, H. B. 1, 1′-(Ethane-1, 2-diyl) bis [3-(4-chlorobenzoyl) thiourea]. Acta. Crystallogr. B. 2011, E67, 112. https://doi.org/10.1107/S2414314616009275

73. Fangzhu, Y. P., Suya, X., Cheng, H. Synthesis of the p-tert-butyl calix[4] arene symmetrical sulfide derivatives and its extraction properties towards U(VI) from aqueous solution. J. Radioanal. Nucl. Chem. 2017, 314, 2137. https://doi.org/10.1007/s10967-017-5608-0

74. Grajda, M., Cmoch, P., Szumna, A. Inherently Chiral Iminoresorcinarenes through Regioselective Unidirectional Tautomerization. J. Org. Chem. 2013, 78, 1. https://doi.org/10.1021/jo4019182

75. Jain, V. K., Kanaiya, E. P. H. Diazo reductive: a new approach to the synthesis of novel “upper rim” functionalized resorcin [4] arene Schiff-bases. J. Incl. Phenom. Macrocycl. Chem. 2008, 62, 111. https://doi.org/10.1007/s10847-008-9445-1

76. Parulekar, S. N., Muppalla, K., Fronczek, F. R., Bisht, K. S. Synthesis of resorcin [4] arene cavitands by ring-closing metathesis. ChemComm. 2007, 46, 4901. https://doi.org/10.1039/B712981E

77. Atwood, J. L., Szumna, A. Hydrogen bonds seal single-molecule capsules. J. Am. Chem. Soc. 2002, 124, 10646. https://doi.org/10.1021/ja027191l

78. Beyeh, N. K., Pan, F., Ras, R. H. N‐Alkyl Ammonium Resorcinarene Chloride Receptors for Guest Binding in Aqueous Environment. Asian J. Org. Chem. 2016, 5, 1027. https://doi.org/10.1002/ajoc.201600187

79. Husain, A. A., Maknenko, A. M., Bisht, K.S. Spatially directional resorcin [4] arene cavitand glycoconjugates for organic catalysis. Chem. Eur. J. 2016, 22, 18. https://doi.org/10.1002/chem.201600352

80. Upadhyay, J. B., Parekh, H. M. Synthesis of supramolecular receptors for amino acid recognition. Curr. Chem. Lett. 2019, 8, 225. http://dx.doi.org/10.5267/j.ccl.2019.6.002

81. Upadhyay, J. B., Parekh, H. M. Resorcin[4]arene Schiff base derivatives: Synthesis, characterization, and extraction studies. J. Chem. Res. 2020, 44, 660–666. https://doi.org/10.1177/1747519820915871

82.  Upadhyay, J. B., Parekh, H. M. Extraction of toxic metal ions by resorcin [4] arene Schiff base derivatives. S. Afr. J. Chem. 2020, 73, 157–162. http://dx.doi.org/10.17159/0379-4350/2020/v73a22


Download all article in PDF

WSN-195-2024-118-157


 

Tags: Calix[4]areneCavitandsGreen ApproachResorcin[4]areneSchiff baseSupramolecules
ShareTweetPin
Next Post

Positive mental health as an antidote to negative social adjustment of in-school adolescents: a review

Exploring Factors Influencing the Adoption of Collaborative Teaching Approaches among Trainee Teachers at Federal Capital Territory College of Education Zuba, Nigeria: Counselling Implications.

View free articles

  • Open access

View Articles

  • 2013 (5)
    • Volume 1 (2013), pp. 1-14 (2)
    • Volume 2 (2013), pp. 1-29 (3)
  • 2014 (13)
    • Volume 3 (2014), pp. 1-21 (3)
    • Volume 4 (2014), pp. 1-16 (2)
    • Volume 5 (2014), pp. 1-36 (4)
    • Volume 6 (2014), pp. 1-23 (3)
  • 2015 (109)
    • Volume 10 (2015), pp. 1-100 (5)
    • Volume 11 (2015), pp. 1-96 (6)
    • Volume 12 (2015), pp. 1-76 (6)
    • Volume 13 (2015), pp. 1-130 (7)
    • Volume 14 (2015), pp. 1-55 (1)
    • Volume 15 (2015), pp. 1-25 (2)
    • Volume 16 (2015), pp. 1-158 (9)
    • Volume 17 (2015), pp. 1-63 (1)
    • Volume 18 (2015), pp. 1-127 (8)
    • Volume 19 (2015), pp. 1-111 (7)
    • Volume 20 (2015), pp. 1-336 (1)
    • Volume 21 (2015), pp. 1-89 (7)
    • Volume 22 (2015), pp. 1-119 (8)
    • Volume 23 (2015), pp. 1-127 (10)
    • Volume 24 (2015), pp. 1-87 (6)
    • Volume 7 (2015), pp. 1-237 (9)
    • Volume 8 (2015), pp. 1-203 (7)
    • Volume 9 (2015), pp. 1-160 (9)
  • 2016 (517)
    • Volume 25 (2016), pp. 1-16 (2)
    • Volume 26 (2016), pp. 1-19 (2)
    • Volume 27 (2016), pp. 1-16 (2)
    • Volume 28 (2016), pp. 1-100 (7)
    • Volume 29 (2016), pp. 1-95 (6)
    • Volume 30 (2016), pp. 1-142 (10)
    • Volume 31 (2016), pp. 1-124 (8)
    • Volume 32 (2016), pp. 1-81 (9)
    • Volume 33 (2016), pp. 1-121 (8)
    • Volume 34 (2016), pp. 1-145 (10)
    • Volume 35 (2016), pp. 1-133 (10)
    • Volume 36 (2016), pp. 1-152 (10)
    • Volume 37 (2016), pp. 1-303 (18)
    • Volume 38 (2016), pp. 1-59 (1)
    • Volume 39 (2016), pp. 1-30 (2)
    • Volume 40 (2016), pp. 1-299 (20)
    • Volume 41 (2016), pp. 1-287 (36)
    • Volume 42 (2016), pp. 1-316 (21)
    • Volume 43(1,2,3) (2016), pp. 1-157 (3)
      • Volume 43, Issue 1 (2016), pp. 1-55 (1)
      • Volume 43, Issue 2 (2016), pp. 56-103 (1)
      • Volume 43, Issue 3 (2016), pp. 104-157 (1)
    • Volume 44 (2016), pp. 1-301 (20)
    • Volume 45(1,2) (2016), pp. 1-383 (21)
      • Volume 45, Issue 1 (2016), pp. 1-62 (1)
      • Volume 45, Issue 2 (2016), pp. 63-383 (20)
    • Volume 46 (2016), pp. 1-286 (20)
    • Volume 47(1,2) (2016), pp. 1-350 (21)
      • Volume 47, Issue 1 (2016), pp. 1-61 (1)
      • Volume 47, Issue 2 (2016), pp. 62-350 (20)
    • Volume 48 (2016), pp. 1-163 (17)
    • Volume 49(1,2) (2016), pp. 1-404 (21)
      • Volume 49, Issue 1 (2016), pp. 1-58 (1)
      • Volume 49, Issue 2 (2016), pp. 59-404 (20)
    • Volume 50 (2016), pp. 1-316 (20)
    • Volume 51 (2016), pp. 1-71 (7)
    • Volume 52 (2016), pp. 1-275 (20)
    • Volume 53(1,2,3) (2016), pp. 1-429 (22)
      • Volume 53, Issue 1 (2016), pp. 1-66 (1)
      • Volume 53, Issue 2 (2016), pp. 67-109 (1)
      • Volume 53, Issue 3 (2016), pp. 110-429 (20)
    • Volume 54 (2016), pp. 1-299 (20)
    • Volume 55 (2016), pp. 1-288 (20)
    • Volume 56 (2015), pp. 1-266 (20)
    • Volume 57 (2016), pp. 1-570 (53)
    • Volume 58 (2016), pp. 1-161 (10)
    • Volume 59 (2016), pp. 1-128 (10)
    • Volume 60 (2016), pp. 1-120 (10)
  • 2017 (481)
    • Volume 61(1,2) (2017), pp. 1-194 (11)
      • Volume 61, Issue 1 (2017), pp. 1-51 (1)
      • Volume 61, Issue 2 (2017), pp. 52-194 (10)
    • Volume 62 (2017), pp. 1-146 (10)
    • Volume 63 (2017), pp. 1-240 (1)
    • Volume 64 (2017), pp. 1-140 (10)
    • Volume 65 (2017), pp. 1-175 (10)
    • Volume 66 (2017), pp. 1-300 (20)
    • Volume 67(1,2,) (2017), pp. 1-389 (21)
      • Volume 67, Issue 1 (2017), pp. 1-67 (1)
      • Volume 67, Issue 2 (2017), pp. 68-389 (20)
    • Volume 68 (2017), pp. 1-141 (1)
    • Volume 69 (2017), pp. 1-253 (20)
    • Volume 70(1,2) (2017), pp. 1-321 (21)
      • Volume 70, Issue 1 (2017), pp. 1-50 (1)
      • Volume 70, Issue 2 (2017), pp. 51-321 (20)
    • Volume 71 (2017), pp. 1-219 (18)
    • Volume 72 (2017), pp. 1-478 (46)
    • Volume 73 (2017), pp. 1-133 (15)
    • Volume 74 (2017), pp. 1-287 (20)
    • Volume 75 (2017), pp. 1-111 (12)
    • Volume 76 (2017), pp. 1-199 (20)
    • Volume 77(1,2) (2017), pp. 1-380 (21)
      • Volume 77, Issue 1 (2017), pp. 1-102 (1)
      • Volume 77, Issue 2 (2017), pp. 103-380 (20)
    • Volume 78 (2017), pp. 1-230 (24)
    • Volume 79 (2017), pp. 1-89 (1)
    • Volume 80 (2017), pp. 1-323 (20)
    • Volume 81(1,2) (2017), pp. 1-312 (21)
      • Volume 81, Issue 1 (2017), pp. 1-47 (1)
      • Volume 81, Issue 2 (2017), pp. 48-312 (20)
    • Volume 82 (2017), pp. 1-90 (1)
    • Volume 83 (2017), pp. 1-239 (20)
    • Volume 84 (2017), pp. 1-92 (1)
    • Volume 85 (2017), pp. 1-73 (10)
    • Volume 86(1,2,3) (2017), pp. 1-370 (22)
      • Volume 86, Issue 1 (2017), pp. 1-58 (1)
      • Volume 86, Issue 2 (2017), pp. 59-122 (1)
      • Volume 86, Issue 3 (2017), pp. 123-370 (20)
    • Volume 87 (2017), pp. 1-255 (20)
    • Volume 88(1,2) (2017), pp. 1-226 (11)
      • Volume 88, Issue 1 (2017), pp. 1-57 (1)
      • Volume 88, Issue 2 (2017), pp. 58-226 (10)
    • Volume 89 (2017), pp. 1-321 (33)
    • Volume 90 (2017), pp. 1-270 (20)
  • 2018 (486)
    • Volume 100 (2018), pp. 1-253 (20)
    • Volume 101 (2018), pp. 1-252 (20)
    • Volume 102 (2018), pp. 1-223 (20)
    • Volume 103 (2018), pp. 1-249 (18)
    • Volume 104 (2018), pp. 1-492 (40)
    • Volume 105 (2018), pp. 1-232 (20)
    • Volume 106 (2018), pp. 1-244 (20)
    • Volume 107 (2018), pp. 1-232 (20)
    • Volume 108 (2018), pp. 1-244 (20)
    • Volume 109 (2018), pp. 1-266 (19)
    • Volume 110 (2018), pp. 1-243 (20)
    • Volume 111 (2018), pp. 1-181 (17)
    • Volume 112 (2018), pp. 1-251 (20)
    • Volume 113 (2018), pp. 1-250 (26)
    • Volume 114 (2018), pp. 1-264 (20)
    • Volume 91 (2018), pp. 1-137 (10)
    • Volume 92(1,2) (2018), pp. 1-399 (21)
      • Volume 92, Issue 1 (2018), pp. 1-138 (1)
      • Volume 92, Issue 2 (2018), pp. 139-399 (20)
    • Volume 93 (2018), pp. 1-141 (15)
    • Volume 94(1,2) (2018), pp. 1-332 (21)
      • Volume 94, Issue 1 (2018), pp. 1-71 (1)
      • Volume 94, Issue 2 (2018), pp. 72-332 (20)
    • Volume 95 (2018), pp. 1-272 (20)
    • Volume 96 (2018), pp. 1-250 (20)
    • Volume 97 (2018), pp. 1-284 (20)
    • Volume 98 (2018), pp. 1-232 (20)
    • Volume 99 (2018), pp. 1-229 (19)
  • 2019 (467)
    • Volume 115 (2019), pp. 1-268 (20)
    • Volume 116 (2019), pp. 1-252 (19)
    • Volume 117 (2019), pp. 1-242 (20)
    • Volume 118 (2019), pp. 1-280 (20)
    • Volume 119 (2019), pp. 1-253 (20)
    • Volume 120(1,2) (2019), pp. 1-295 (21)
      • Volume 120, Issue 1 (2019), pp. 1-59 (1)
      • Volume 120, Issue 2 (2019), pp. 60-295 (20)
    • Volume 121 (2019), pp. 1-100 (13)
    • Volume 122 (2019), pp. 1-262 (20)
    • Volume 123 (2019), pp. 1-273 (20)
    • Volume 124(1,2) (2019), pp. 1-333 (21)
      • Volume 124, Issue 1 (2019), pp. 1-85 (1)
      • Volume 124, Issue 2 (2019), pp. 86-1-333 (20)
    • Volume 125 (2019), pp. 1-259 (20)
    • Volume 126 (2019), pp. 1-298 (20)
    • Volume 127(1,2,3) (2019), pp. 1-376 (22)
      • Volume 127, Issue 1 (2019), pp. 1-55 (1)
      • Volume 127, Issue 2 (2019), pp. 56-105 (1)
      • Volume 127, Issue 3 (2019), pp. 106-376 (20)
    • Volume 128(1,2) (2019), pp. 1-432 (21)
      • Volume 128, Issue 1 (2019), pp. 1-70 (1)
      • Volume 128, Issue 2 (2019), pp. 71-432 (20)
    • Volume 129 (2019), pp. 1-267 (20)
    • Volume 130 (2019), pp. 1-308 (20)
    • Volume 131 (2019), pp. 1-288 (20)
    • Volume 132 (2019), pp. 1-312 (24)
    • Volume 133 (2019), pp. 1-274 (20)
    • Volume 134(1,2) (2020), pp. 1-338 (21)
      • Volume 134, Issue 1 (2019), pp. 1-51 (1)
      • Volume 134, Issue 2 (2019), pp. 52-338 (20)
    • Volume 135 (2019), pp. 1-298 (22)
    • Volume 136 (2019), pp. 1-246 (16)
    • Volume 137 (2019), pp. 1-236 (14)
    • Volume 138(1,2) (2019), pp. 1-294 (13)
      • Volume 138, Issue 1 (2019), pp. 1-64 (1)
      • Volume 138, Issue 2 (2019), pp. 65-294 (12)
  • 2020 (179)
    • Volume 139(1,2) (2020), pp. 1-258 (13)
      • Volume 139, Issue 1 (2020), pp. 1-60 (1)
      • Volume 139, Issue 2 (2020), pp. 61-258 (12)
    • Volume 140 (2020), pp. 1-184 (10)
    • Volume 141 (2020), pp. 1-155 (10)
    • Volume 142 (2020), pp. 1-194 (12)
    • Volume 143 (2020), pp. 1-261 (16)
    • Volume 144 (2020), pp. 1-449 (30)
    • Volume 145 (2020), pp. 1-408 (30)
    • Volume 146 (2020), pp. 1-289 (18)
    • Volume 147 (2020), pp. 1-208 (12)
    • Volume 148 (2020), pp. 1-121 (8)
    • Volume 149 (2020), pp. 1-165 (10)
    • Volume 150 (2020), pp. 1-181 (10)
  • 2021 (143)
    • Volume 151 (2021), pp. 1-122 (8)
    • Volume 152 (2021), pp. 1-125 (8)
    • Volume 153(1,2) (2021), pp. 1-215 (13)
      • Volume 153, Issue 1 (2021), pp. 1-42 (1)
      • Volume 153, Issue 2 (2021), pp. 43-215 (12)
    • Volume 154 (2021), pp. 1-174 (10)
    • Volume 155 (2021), pp. 1-154 (10)
    • Volume 156 (2021), pp. 1-191 (12)
    • Volume 157 (2021), pp. 1-188 (10)
    • Volume 158 (2021), pp. 1-298 (16)
    • Volume 159 (2021), pp. 1-223 (14)
    • Volume 160 (2021), pp. 1-337 (20)
    • Volume 161 (2021), pp. 1-156 (10)
    • Volume 162 (2021), pp. 1-178 (12)
  • 2022 (125)
    • Volume 163 (2022), pp. 1-157 (8)
    • Volume 164 (2022), pp. 1-149 (8)
    • Volume 165 (2022), pp. 1-209 (12)
    • Volume 166 (2022), pp. 1-145 (10)
    • Volume 167 (2022), pp. 1-161 (9)
    • Volume 168 (2022), pp. 1-146 (10)
    • Volume 169 (2022), pp. 1-201 (10)
    • Volume 170 (2022), pp. 1-171 (10)
    • Volume 171 (2022), pp. 1-125 (8)
    • Volume 172 (2022), pp. 1-333 (20)
    • Volume 173 (2022), pp. 1-161 (10)
    • Volume 174 (2022), pp. 1-176 (10)
  • 2023 (132)
    • Volume 175 (2023), pp. 1-108 (8)
    • Volume 176 (2023), pp. 1-174 (10)
    • Volume 177 (2023), pp. 1-136 (8)
    • Volume 178 (2023), pp. 1-165 (10)
    • Volume 179 (2023), pp. 1-164 (10)
    • Volume 180 (2023), pp. 1-162 (12)
    • Volume 181 (2023), pp. 1-215 (12)
    • Volume 182 (2023), pp. 1-265 (18)
    • Volume 183 (2023), pp. 1-226 (14)
    • Volume 184 (2023), pp. 1-154 (10)
    • Volume 185 (2023), pp. 1-191 (10)
    • Volume 186 (2023), pp. 1-160 (10)
  • 2024 (183)
    • Volume 187 (2024), pp. 1-156 (10)
    • Volume 188 (2024), pp. 1-197 (12)
    • Volume 189 (2024), pp. 1-310 (20)
    • Volume 190(1,2) (2024), pp. 1-351 (18)
      • Volume 190, Issue 1 (2024), pp. 1-69 (1)
      • Volume 190, Issue 2 (2024), pp. 70-351 (17)
    • Volume 191 (2024), pp. 1-207 (12)
    • Volume 192 (2024), pp. 1-319 (20)
    • Volume 193(1,2) (2024), pp. 1-252 (13)
      • Volume 193, Issue 1 (2024), pp. 1-45 (1)
      • Volume 193, Issue 2 (2024), pp. 46-252 (12)
    • Volume 194 (2024), pp. 1-213 (13)
    • Volume 195 (2024), pp. 1-235 (13)
    • Volume 196 (2024), pp. 1-221 (14)
    • Volume 197 (2024), pp. 1-231 (15)
    • Volume 198 (2024), pp. 1-402 (23)
  • 2025 (169)
    • Volume 199 (2025), pp. 1-253 (16)
    • Volume 200 (2025), pp. 1-223 (14)
    • Volume 201 (2025), pp. 1-245 (12)
    • Volume 202 (2025), pp. 1-317 (17)
    • Volume 203 (2025), pp. 1-438 (15)
    • Volume 204 (2025), pp. 1-353 (19)
    • Volume 205 (2025), pp. 1-272 (16)
    • Volume 206 (2025), pp. 1-172 (13)
    • Volume 207 (2025), pp. 1-173 (12)
    • Volume 208 (2025), pp. 1-174 (11)
    • Volume 209 (2025), pp. 1-184 (12)
    • Volume 210 (2025), pp. 1-158 (12)
  • 2026 (28)
    • Volume 211 (2026), pp. 1-348 (21)
    • Volume 212 (2026), pp. (7)
  • Info (6)
  • News (3)
  • Open access (467)
  • Premium (39)

Last Articles

  • All
  • Premium
  • Open access

Synthesis, characterization and docking studies of some novel xanthene derivatives

2024-01-18

Antimicrobial effects and phytochemical analysis of Psidium gujava leaf extract against Pseudomonas aeruginosa

2024-05-16

Usage of acupuncture in neurosurgical conditions

2024-02-15

Popular Articles

  • About Us

    About Us

    0 shares
    Share 0 Tweet 0
  • Submit your Article

    0 shares
    Share 0 Tweet 0
  • Jeevamrut – A Natural Fertilizer

    0 shares
    Share 0 Tweet 0
  • Abstracting & Indexing

    0 shares
    Share 0 Tweet 0
  • Guide for Authors

    0 shares
    Share 0 Tweet 0

Careers

  • All
  • Careers
No Content Available
World Scientific News

World Scientific News (WSN) is an open-access fully peer-reviewed scholarly journal. The monthly – interdisciplinary journal is directed in the first place to scientists who want to publish their findings, insights, observations, conclusions, etc.

READ MORE

Menu

  • Home
  • About Us
  • Editorial Board
  • Guide for Authors
  • Instruction for Authors
  • Abstracting & Indexing
  • Submit your Article
  • Careers
  • News

Other databases

Crossref

CAS
Google Scholar
Google Scholar Metrics
ICZN
ProQuest
Road Directory
ZooBank

AGRO

 

EISSN 2392-2192

Login / Register
Privacy Policy
Cookie Policy

made by fixfix

No Result
View All Result
  • Home
  • About
    • About Us
    • Editorial Board
    • Guide for Authors
    • Abstracting & Indexing
    • Instruction for Authors
    • Submit your Article
  • View Articles
    • 2026
    • 2025
    • 2024
    • 2023
    • 2022
    • 2021
    • 2020
    • 2019
    • 2018
    • 2017
    • 2016
    • 2015
    • 2014
    • 2013
  • Careers
  • News

made by fixfix

Welcome Back!

Login to your account below

Forgotten Password?

Retrieve your password

Please enter your username or email address to reset your password.

Log In
Are you sure want to unlock this post?
Unlock left : 0
Are you sure want to cancel subscription?
We use cookies to ensure that we give you the best experience on our website. If you continue to use this site we will assume that you are happy with it.