Alkoxysulfenylation of alkenes: Development and recent advances
Cao Y. Soleimani-Amiri S. Ahmadi R. Issakhov A. Ebadi A.G. Vessally E.
24 August 2021Royal Society of Chemistry
RSC Advances
2021#11Issue 5132513 - 32525 pp.
Among the wide variety of synthetic transformations of inexpensive and abundant feedstock alkenes, vicinal difunctionalization of carbon-carbon double bonds represent one of the most powerful and effective strategies for the introduction of two distinct functional groups into target compounds in a one-pot process. In this context, the direct alkoxysulfenylation of alkenes has emerged as an elegant method to construct valuable β-alkoxy sulfides in an atom- and pot-economic manner utilizing readily accessible starting materials. Here, we review the available literature on this appealing research topic by hoping that it will be beneficial for eliciting further research and thinking in this domain. This journal is
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School of Mechatronic Engineering, XiAn Technological University, Xian, 710021, China
Department of Chemistry, Karaj Branch, Islamic Azad University, Karaj, Iran
Department of Chemistry, College of Basic Sciences, Yadegar-e-Imam Khomeini (RAH), Shahre Rey Branch, Islamic Azad University, Tehran, Iran
Department of Mathematical and Computer Modelling, Al-Farabi Kazakh National University, Almaty, 050040, Kazakhstan
Department of Mathematics and Cybernetics, Kazakh British Technical University, Almaty, 050000, Kazakhstan
Department of Agriculture, Jouybar Branch, Islamic Azad University, Jouybar, Iran
Department of Chemistry, Payame Noor University, P.O. Box 19395-3697, Tehran, Iran
School of Mechatronic Engineering
Department of Chemistry
Department of Chemistry
Department of Mathematical and Computer Modelling
Department of Mathematics and Cybernetics
Department of Agriculture
Department of Chemistry
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