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Russian Chemical Reviews, 1995, Volume 64, Issue 8, Pages 731–751
DOI: https://doi.org/10.1070/RC1995v064n08ABEH000172
(Mi rcr1248)
 

This article is cited in 30 scientific papers (total in 30 papers)

Sylfenyl chlorides in organic synthesis

I. V. Koval'

Ukrainian University of Chemical Engineering, Dnepropetrovsk
Abstract: The results of studies concerned with the use of sulfenyl chlorides in organic synthesis are described systematically and surveyed. The methods of synthesis of sulphenyl chlorides are also considered. The bibliography includes 271 references.
Received: 12.01.1995
Bibliographic databases:
Document Type: Article
UDC: 547.425.5
Language: English
Original paper language: Russian


Citation: I. V. Koval', “Sylfenyl chlorides in organic synthesis”, Usp. Khim., 64:8 (1995), 781–802; Russian Chem. Reviews, 64:8 (1995), 731–751
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  • https://www.mathnet.ru/eng/rcr1248
  • https://doi.org/10.1070/RC1995v064n08ABEH000172
  • https://www.mathnet.ru/eng/rcr/v64/i8/p781
  • This publication is cited in the following 30 articles:
    1. Andrés García-Domínguez, Nathan M. West, Robert T. Hembre, Guy C. Lloyd-Jones, ACS Catal., 13:14 (2023), 9487  crossref
    2. R. S. Ishigeev, S. V. Amosova, V. A. Potapov, Russ J Gen Chem, 93:S1 (2023), S87  crossref
    3. Harikesh Kumar, Atul Dubey, Gurudayal Prajapati, Ruchir Kant, Ravi S. Ampapathi, Pintu Kumar Mandal, New J. Chem., 46:7 (2022), 3426  crossref
    4. Murshida Karim, Nizamuddin Ahmed, Asian J. Chem., 34:8 (2022), 2061  crossref
    5. Musalov M.V. Maylyan A.A. Musalova M.V. Amosova S.V. Potapov V.A., Russ. Chem. Bull., 70:2 (2021), 420–423  isi
    6. Vladimir A. Potapov, Roman S. Ishigeev, Svetlana V. Amosova, Molecules, 26:4 (2021), 1116  crossref
    7. Vladimir A. Potapov, Roman S. Ishigeev, Svetlana V. Amosova, Molecules, 26:16 (2021), 4844  crossref
    8. Vladimir A. Potapov, Roman S. Ishigeev, Lyudmila A. Belovezhets, Irina V. Shkurchenko, Svetlana V. Amosova, Applied Sciences, 11:18 (2021), 8532  crossref
    9. Yan Cao, Shahrzad Abdolmohammadi, Roya Ahmadi, Alibek Issakhov, Abdol Ghaffar Ebadi, Esmail Vessally, RSC Adv., 11:51 (2021), 32394  crossref
    10. M. V. Musalov, A. A. Maylyan, M. V. Musalova, S. V. Amosova, V. A. Potapov, Russ Chem Bull, 70:2 (2021), 420  crossref
    11. Vladimir A. Potapov, Roman S. Ishigeev, Lyudmila A. Belovezhets, Svetlana V. Amosova, Molecules, 26:18 (2021), 5579  crossref
    12. Vladimir A. Potapov, Roman S. Ishigeev, Svetlana V. Amosova, Tatyana N. Borodina, Tetrahedron Letters, 60:6 (2019), 475  crossref
    13. Yakan H. Kutuk H., Mon. Chem., 149:11 (2018), 2047–2057  crossref  isi  scopus
    14. Jatuporn Meesin, Manat Pohmakotr, Vichai Reutrakul, Darunee Soorukram, Pawaret Leowanawat, Chutima Kuhakarn, Org. Biomol. Chem., 15:17 (2017), 3662  crossref
    15. Vera P. Demertzidou, Stavroula Pappa, Vasiliki Sarli, Alexandros L. Zografos, J. Org. Chem., 82:16 (2017), 8710  crossref
    16. Bei-Bei Liu, Xue-Qiang Chu, Huan Liu, Ling Yin, Shun-Yi Wang, Shun-Jun Ji, J. Org. Chem., 82:19 (2017), 10174  crossref
    17. Tirri T. Aubert M. Pawelec W. Holappa A. Wilen C.-E., Polymers, 8:10 (2016), 360  crossref  isi
    18. Li Ya., Zhu F., Wang Z., Wu X.-F., Chem.-Asian J., 11:24 (2016), 3503–3507  crossref  isi
    19. Hong Qi, Tongxin Zhang, Kefeng Wan, Meiming Luo, J. Org. Chem., 81:10 (2016), 4262  crossref
    20. Salavat S. Ashirbaev, Vitalij V. Levin, Marina I. Struchkova, Alexander D. Dilman, Journal of Fluorine Chemistry, 191 (2016), 143  crossref
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