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Russian Chemical Reviews, 1996, Volume 65, Issue 5, Pages 421–440
DOI: https://doi.org/10.1070/RC1996v065n05ABEH000218
(Mi rcr1294)
 

This article is cited in 28 scientific papers (total in 28 papers)

Synthesis and application of sulfenamides

I. V. Koval'

Ukrainian State University of Chemical Engineering, Dnepropetrovsk
Abstract: The results of studies on the use of sulfenamides in organic synthesis are systematised and generalised. The fields of industrial application of sulfenamides are considered. The bibliography includes 220 references.
Received: 15.08.1995
Bibliographic databases:
Document Type: Article
UDC: 547.425.5
Language: English
Original paper language: Russian


Citation: I. V. Koval', “Synthesis and application of sulfenamides”, Usp. Khim., 65:5 (1996), 452–473; Russian Chem. Reviews, 65:5 (1996), 421–440
Linking options:
  • https://www.mathnet.ru/eng/rcr1294
  • https://doi.org/10.1070/RC1996v065n05ABEH000218
  • https://www.mathnet.ru/eng/rcr/v65/i5/p452
  • This publication is cited in the following 28 articles:
    1. Şukriye Çakmak, Tuğba Aycan, Hasan Yakan, Aysel Veyisoğlu, Hasan Tanak, Meryem Evecen, Acta Crystallogr C Struct Chem, 79:6 (2023), 249  crossref
    2. Jessica T. Liu, Daniel S. Brandes, Nathaniel S. Greenwood, Jonathan A. Ellman, Synthesis, 55:15 (2023), 2353  crossref
    3. Ziqian Bai, Shiyang Zhu, Yiyao Hu, Peng Yang, Xin Chu, Gang He, Hao Wang, Gong Chen, Nat Commun, 13:1 (2022)  crossref
    4. Hatice Mutlu, Patrick Theato, Sulfur‐Containing Polymers, 2021, 191  crossref
    5. Makitalo C.L., Yoshimura A., Rohde G.T., Mironova I.A., Yusubova R.Y., Yusubov M.S., Zhdankin V.V., Saito A., Eur. J. Org. Chem., 2020:41 (2020), 6433–6439  crossref  isi
    6. Mutlu H., Theato P., Macromol. Rapid Commun., 41:13 (2020), 2000181, 2000181  crossref  isi
    7. Guin A., Rathod T., Gaykar R.N., Roy T., Biju A.T., Org. Lett., 22:6 (2020), 2276–2280  crossref  isi
    8. Petkowski J.J., Bains W., Seager S., Astrobiology, 19:4 (2019), 579–613  crossref  isi  scopus
    9. Halimehjani A.Z., Klepetarova B., Beier P., Tetrahedron, 74:15 (2018), 1850–1858  crossref  isi  scopus
    10. Nasab Fatemeh Alsadat Hosseini, Fekri L.Z., Monfared A., Hosseinian A., Vessally E., RSC Adv., 8:33 (2018), 18456–18469  crossref  isi  scopus
    11. Yakan H. Kutuk H., Mon. Chem., 149:11 (2018), 2047–2057  crossref  isi  scopus
    12. Yang L. Li Sh. Dou Y. Zhen Sh. Li H. Zhang P. Yuan B. Yang G., Asian J. Org. Chem., 6:3 (2017), 265–268  crossref  isi  scopus
    13. Monteiro Maria Lucia G., Marsico E.T., Canto Anna Carolina V. da C. S., da Costa-Lima B.R.C., da Costa M.P., Viana F.M., da Silva T.J.P., Conte-Junior C.A., J. Food Sci., 82:4 (2017), 1028–1036  crossref  isi  scopus
    14. Musiejuk M., Witt D., Phosphorus Sulfur Silicon Relat. Elem., 191:2, SI (2016), 305–310  crossref  isi  scopus
    15. Javorskis T., Bagdziunas G., Orentas E., Chem. Commun., 52:23 (2016), 4325–4328  crossref  isi  scopus
    16. Tirri T. Aubert M. Pawelec W. Holappa A. Wilen C.-E., Polymers, 8:10 (2016), 360  crossref  isi  scopus
    17. Saidalimu I., Guo M., Tokunaga E., Shibata N., Asian J. Org. Chem., 5:10 (2016), 1208–1212  crossref  isi  scopus
    18. Shiro D., Fujiwara Sh.-i., Tsuda S., Iwasaki T., Kuniyasu H., Kambe N., Tetrahedron Lett., 56:12 (2015), 1531–1534  crossref  isi  elib  scopus
    19. Pluta R., Rueping M., Chem.-Eur. J., 20:52 (2014), 17315–17318  crossref  isi  scopus
    20. Greene's Protective Groups in Organic Synthesis, 2014, 895  crossref
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