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Metal- and oxidant-free electrochemical synthesis of sulfinic esters from thiols and alcohols
Ist Teil von
Green chemistry : an international journal and green chemistry resource : GC, 2019, Vol.21 (2), p.5528-5531
Ort / Verlag
Cambridge: Royal Society of Chemistry
Erscheinungsjahr
2019
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
An efficient and eco-friendly electrochemical synthesis of various sulfinic esters from thiols and alcohols
via
sequential S-H/S bond cleavage and double S-O bond formation under mild reaction conditions has been developed. Stoichiometric oxidants, metal catalysts, activating agents and even added bases were avoided in this method, and the only by-product generated from this reaction was dihydrogen gas which could serve as a green source of energy. Various functional groups are compatible with this green protocol which can be easily conducted on a gram-scale.
An eco-friendly electrochemical synthesis of sulfinic esters from thiols and alcohols under mild reaction conditions has been developed.