100498-97-3Relevant articles and documents
Selective C-H chalcogenation of thiazoles: Via thiazol-2-yl-phosphonium salts
Zi, You,Wagner, Konrad,Sch?mberg, Fritz,Vilotijevic, Ivan
, p. 5183 - 5191 (2020)
Thiazoles and benzothiazoles undergo regioselective C2-H chalcogenation via the sequence of thiazole C2-functionalization with phosphines to produce phosphonium salts which in turn react with S- and Se-centered nucleophiles to give products of C2-H chalco
Facile synthesis of a series of non-symmetric thioethers including a benzothiazole moiety and their use as effcient in vitro anti-trypanosoma cruzi agents
Avila-Sorrosa, Alcives,Tapia-Alvarado, Jazz D.,Nogueda-Torres, Benjamín,Chacón-Vargas, Karla Fabiola,Díaz-Cedillo, Francisco,Vargas-Díaz, María Elena,Morales-Morales, David
, (2019/09/03)
A series of 2-benzylsulfanyl benzothiazole (BTA) derivatives were synthesized and fully characterized and in vitro tested against two strains of T. cruzi (NINOA and INC-5), exhibiting good activities at low concentrations.
A Practical Access to Functionalized Alkyl Sulfinates
Tran,Flamme,Chagnes,Haddad,Phansavath,Ratovelomanana-Vidal
supporting information, p. 1622 - 1626 (2018/06/12)
We describe herein a three-step synthesis of aliphatic sulfinates. This cost-effective method involves the use of 2-mercaptobenzothiazole under mild conditions and exhibits good yields (up to 78% over three steps). This approach provides an access to a wi
