22158-12-9Relevant academic research and scientific papers
NFSI-catalyzed S[sbnd]S bond exchange reaction for the synthesis of unsymmetrical disulfides
Hu, Qingyue,Li, Zheng-Yi,Song, Mengjie,Sun, Xiaoqiang,Yang, Ke
supporting information, (2022/01/26)
The metal-free S[sbnd]S bond exchange reaction of symmetrical disulfides catalyzed by NFSI is described. This novel protocol provides a facile and efficient approach to accessing important unsymmetrical disulfides. Furthermore, this strategy could also be utilized in the late-stage functionalization of amino acids, drugs, and natural products. The broad substrate scope, good functional group tolerance and easy accessibility of catalyst indicate that this strategy affords a green and practical complementary method to various unsymmetrical disulfides.
Disulfiram-based disulfides as narrow-spectrum antibacterial agents
Sheppard, Jordan G.,Frazier, Keely R.,Saralkar, Pushkar,Hossain, Mohammad F.,Geldenhuys, Werner J.,Long, Timothy E.
, p. 1298 - 1302 (2018/03/26)
Sixteen disulfides derived from disulfiram (Antabuse) were evaluated as antibacterial agents. Derivatives with hydrocarbon chains of seven and eight carbons in length exhibited antibacterial activity against Gram-positive Staphylococcus, Streptococcus, En
Aminecarbotrithioates
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, (2008/06/13)
A thiolsulfonate is reacted with an aminecarbodithioate salt to give an aminecarbotrithioate product. The products of this invention have biological activity, particularly in controlling microorganisms and other pests.
