5728-82-5Relevant academic research and scientific papers
Thioderivatives of Resorcin[4]arene and Pyrogallol[4]arene: Are Thiols Tolerated in the Self-Assembly Process?
Nemat, Suren J.,Tiefenbacher, Konrad
supporting information, p. 6861 - 6865 (2021/09/14)
Three novel thiol bearing resorcin[4]arene and pyrogallol[4]arene derivatives were synthesized. Their properties were studied with regards to self-assembly, disulfide chemistry, and Br?nsted acid catalysis. This work demonstrates that (1) one aromatic thiol on the resorcin[4]arene framework is tolerated in the self-assembly process to a hexameric hydrogen bond-based capsule, (2) thio-derivatized resorcin[4]arene analogs can be covalently linked through disulfides, and (3) the increased acidity of aromatic thio-substituent is not sufficient to replace HCl as cocatalyst for capsule catalyzed terpene cyclizations.
Bis(2,6-dimethoxyphenyl) sulfide, selenide and telluride, and their derivatives
Wada, Masanori,Nobuki, Shin-Ichi,Tenkyuu, Yoshinori,Natsume, Satoko,Asahara, Masahiro,Erabi, Tatsuo
, p. 282 - 289 (2007/10/03)
2,6-Dimethoxyphenyl derivatives of sulfur, selenium, and tellurium, such as ΦEEΦ, Φ2E, ΦSeH, [MeΦ2E]X (X = MeSO4, ClO4), Φ2EO · xH2O, [Φ2EOH]ClO4, [Φ2EOR]Cl
Reductive Coupling of Aromatic Sulfinate Salts to Disulfides
Pinnick, Harold W.,Reynolds, Michael A.,McDonald, Robert T.,Brewster, Wanda D.
, p. 930 - 932 (2007/10/02)
A variety of aromatic sulfinate salts undergo reductive coupling to disulfides in the presence of ethyl hypophosphite.Support for the intermediacy of sulfoxy sulfones and thiosulfonates has been obtained.
