CC BY 4.0 · SynOpen 2023; 07(03): 371-373
DOI: 10.1055/a-2134-9007
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Copper Sulfate (CuSO4): An Efficient Reagent in Organic Synthesis

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Euzébio G. Barbosa
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Abstract



Publication History

Received: 11 May 2023

Accepted after revision: 19 July 2023

Accepted Manuscript online:
21 July 2023

Article published online:
15 August 2023

© 2023. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by/4.0/)

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  • References

  • 1 The Merck Index, 11th ed . Budavari S. Merck & Co; Rahway: 1989
  • 2 Ruggiero MT, Erba A, Orlando R, Korter TM. Phys. Chem. Chem. Phys. 2015; 17: 31023
  • 3 Aquilina G, Bach A, Bampidis V, Bastos ML, Flachowsky G, Gasa-Gasó J, Gralak M, Hogstrand C, Leng L, López-Puente S, Martelli G, Mayo B, Renshaw D, Rychen D, Saarela M, Sejrsen K, Beelen PV, Wallace RJ, Westendorf J. EFSA J. 2012; 10: 12
  • 4 Manto M. Toxics 2014; 2: 327
  • 5 Güner EK, Kancan D, Naktiyok J, Özer A. Asia-Pac. J. Chem. Eng. 2021; 16: e2583
  • 6 Hann RM, Hudson CS. American Chemical Society 1944; 66: 735
  • 7 Tao C.-Z, Cui X, Li J, Liu A.-X, Liu L, Guo Q.-X. Tetrahedron Lett. 2007; 48: 3525
  • 8 Gonzaga D, Da Silva FC, Ferreira VF, Wardell JL, Wardell SM. S. V. J. Chem. Crystallogr. 2016; 46: 67
  • 9 Decuypere E, Bernard S, Feng M, Porte K, Riomet M, Thuéry P, Audisio D, Taran F. ACS Catal. 2018; 8: 11882
  • 10 Ficker M, Svenningsen SW, Larribeau T, Christensen JB. Tetrahedron Lett. 2018; 59: 1125
  • 11 Al-Qahtani SD, Alsoliemy A, Almehmadi SJ, Alkhamis K, Alrefaei AF, Zaky R, El-Metwaly N. J. Mol. Struct. 2021; 1244
  • 12 Chaudhari PR, Bhise NB, Singh GP, Bhat V, Shenoy GG. J. Chem. Sci. 2022; 134: 56
  • 13 Vrbata D, Filipová M, Tavares MR, Cerveny J, Vlachova M, Sirova M, Pelantova H, Petraskova L, Bumba L, Konefał R, Etrych T, Kren V, Chytil P, Bojarová P. J. Med. Chem. 2022; 65: 3866
  • 14 Fan H, Tong Z, Ren Z, Mishra K, Morita S, Edouarzin E, Gorla L, Averkiev B, Day VW, Hua DH. J. Org. Chem. 2022; 87: 6742
  • 15 Groch JR, Lauta NR, Njardarson JT. Org. Lett. 2023; 25: 395
  • 16 Hunt-Painter AA, Deeble BM, Stocker BL, Timmer MS. M. ACS Omega 2022; 7: 28756
  • 17 Banerjee A, Saha S, Maji MS. J. Org. Chem. 2022; 87: 4343
  • 18 Seki M, Takahashi Y. J. Org. Chem. 2021; 86: 7842
  • 19 Shan X.-H, Yang B, Qu J.-P, Kang Y.-B. Chem. Commun. 2020; 56: 4063