Cryovoltammetrically probing functional group reductive cleavage: alkyl-sulfur versus aryl-sulfur bond cleavage in an alkyl naphthyl thioether under single electron-transfer is temperature switchable.
A series of single electron-transfer (SET) reactions on a naphthyl thioether have shown that the reductive cleavage mechanism changes at low temperatures and this selectivity is proved using an electrochemical analysis that mimics the SET reaction conditions.
Päätekijät: | Paddon, C, Bhatti, F, Donohoe, T, Compton, R |
---|---|
Aineistotyyppi: | Journal article |
Kieli: | English |
Julkaistu: |
2006
|
Samankaltaisia teoksia
-
Electrocatalytic reduction of alkyl iodides in tetrahydrofuran at silver electrodes
Tekijä: Paddon, C, et al.
Julkaistu: (2007) -
Expedient Synthesis of Alkyl and Aryl Thioethers Using Xanthates as Thiol-Free Reagents
Tekijä: Jinli Nie, et al.
Julkaistu: (2024-05-01) -
C(alkyl)–C(vinyl) bond cleavage enabled by Retro-Pallada-Diels-Alder reaction
Tekijä: Qingyang Zhao, et al.
Julkaistu: (2023-05-01) -
Rhodium-Catalyzed Synthesis of Organosulfur Compounds Involving S-S Bond Cleavage of Disulfides and Sulfur
Tekijä: Mieko Arisawa, et al.
Julkaistu: (2020-08-01) -
Cryo-electrochemistry in tetrahydrofuran: The electrochemical reduction of a phenyl thioether: [(3-{[trans-4-(methoxymethoxy)cyclohexyl]oxy}propyl)thio]benzene
Tekijä: Paddon, C, et al.
Julkaistu: (2006)