82422-32-0Relevant academic research and scientific papers
Base-promoted ring opening of 3-chlorooxindoles for the construction of 2-aminoarylthioates and their transformation to quinazolin-4(3: H)-ones
Poudel, Tej Narayan,Khanal, Hari Datta,Lee, Yong Rok
supporting information, p. 4735 - 4741 (2018/03/21)
An unprecedented methodology for the preparation of diverse S-alkyl 2-aminoarylthioates has been developed based on cesium carbonate-promoted direct ring opening of 3-chlorooxindoles with thiols. This novel protocol proceeds via cascade sulfenylation, aer
Decarboxylation of isatoic anhydrides with disulfides: An efficient and general synthesis of S-aryl 2-aminobenzothioate derivatives
Liu, Miaochang,Lin, Shaomiao,Ding, Jinchang,Gao, Wenxia,Wu, Huayue,Chen, Jiuxi
, p. 2283 - 2288 (2013/04/10)
The decarboxylation of isatoic anhydrides with disulfides was realized in the presence of sodium dithionite, leading to S-aryl 2-aminobenzothioate derivatives in moderate to excellent yields. Furthermore, the decarboxylation of diphenyldiselenide with isa
A simple acylation of thiols with anhydrides
Temperini, Andrea,Annesi, Diego,Testaferri, Lorenzo,Tiecco, Marcello
supporting information; experimental part, p. 5368 - 5371 (2010/10/20)
Different thiols were efficiently acylated at room temperature with different anhydrides in the presence of potassium carbonate. Chemoselective protection of thiol in the presence of hydroxy group was achieved using di-tert-butyl dicarbonate and isatoic anhydride.
