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- W4381734241 endingPage "2331" @default.
- W4381734241 startingPage "2310" @default.
- W4381734241 abstract "Alkenes are valuable feedstocks in organic synthesis. Selenium or sulfur-containing coumpounds with a neighboring functional group can be easily prepared by direct difunctionalization of alkenes via three-component reactions. It will reduce the number of steps and waste generation, and form complicated molecules from simple starting materials. Herein, recent developments (2013–2022) have been summarized via two categories: (1) selenylation via seleniranium intermediates or Se-centered radicals; (2) thiolation with more diverse mechanisms and products Reactions with electron-rich arenes, alcohols, water, acids, NaN3, amines, KSCN, and sulfamides, TMSNCS, TMSN3, Et3N ⋅ 3HF, SOCl2, HCl, NFSI, tBuONO, pyridinium salts, tBuOOH, ArN2BF4, CO2, CO, O2, CF3SO2Cl, R2P(O)−H, (RO)2P(O)SH, (RO)2P(O)OH et al will be discussed. We hope this review will do help for future research in this area." @default.
- W4381734241 created "2023-06-24" @default.
- W4381734241 creator A5008526964 @default.
- W4381734241 creator A5024026873 @default.
- W4381734241 creator A5031219561 @default.
- W4381734241 creator A5035752408 @default.
- W4381734241 creator A5082119092 @default.
- W4381734241 date "2023-07-04" @default.
- W4381734241 modified "2023-09-27" @default.
- W4381734241 title "Recent Developments in Selenylation and Thiolation of Alkenes via Three‐component Reactions" @default.
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