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Makale Tam Makale Uluslararası 2024

Catalyst/Metal/Solvent-Free Markovnikov Hydrothiolation of Unactivated Alkenes with Dithiocarbamic Acids

Azim Ziyaei Halimehjani, Ziya Dağalan, Zahra Marjani, Figen Gunduz, Arif Daştan, Bilal Nişancı

JOURNAL OF ORGANIC CHEMISTRY Cilt 89 · Sayı 8 · ss. 5353–5362 · 19.04.2024
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Özet

Catalyst-free Markovnikov-selective hydrothiolation of unactivated alkenes still remains a great challenge. Herein, we develop a catalyst/metal/solvent-free methodology for the Markovnikov hydrothiolation of unactivated alkenes with in situ prepared dithiocarbamic acids, providing a wide array of alkyl dithiocarbamates. A variety of terminal, internal, cyclic, and acyclic unactivated alkenes were applied successfully in this protocol. This three-component thiol-ene reaction can be considered as a new family of click reactions.

Atıf için künye

Halimehjani, A. Z., Dağalan, Z., Marjani, Z., Gunduz, F., Daştan, A., & Nişancı, B. (2024). Catalyst/Metal/Solvent-Free Markovnikov Hydrothiolation of Unactivated Alkenes with Dithiocarbamic Acids. JOURNAL OF ORGANIC CHEMISTRY, 89(8), 5353–5362. https://doi.org/10.1021/acs.joc.3c02722

BibTeX
@article{halimehjani2024-54189,
  author = {Halimehjani, Azim Ziyaei and Dağalan, Ziya and Marjani, Zahra and Gunduz, Figen and Daştan, Arif and Nişancı, Bilal},
  title = {Catalyst/Metal/Solvent-Free Markovnikov Hydrothiolation of Unactivated Alkenes with Dithiocarbamic Acids},
  journal = {JOURNAL OF ORGANIC CHEMISTRY},
  year = {2024},
  volume = {89},
  number = {8},
  pages = {5353--5362},
  issn = {0022-3263},
  doi = {10.1021/acs.joc.3c02722},
  url = {https://akademik.atauni.edu.tr/yayinlar/54189-catalystmetalsolvent-free-markovnikov-hydrothiolation-of-unactivated-alkenes}
}