An article In Situ Activation of Disulfides for Multicomponent Reactions with Isocyanides and a Broad Range of Nucleophiles WOS:000460491700052 published article about ISOTHIOUREAS; EQUIVALENT; ACCESS; VITRO in [Lei, Xiaofang; Wang, Yuanyuan; Sun, Zhihua] Shanghai Univ Engn Sci, Coll Chem & Chem Engn, 333 Longteng Rd, Shanghai 201620, Peoples R China; [Fan, Erkang] Univ Washington, Dept Biochem, 1705 NE Pacific St, Seattle, WA 98195 USA in 2019.0, Cited 27.0. The Name is Benzyl Alcohol. Through research, I have a further understanding and discovery of 100-51-6. COA of Formula: C7H8O
Activation of disulfides with N-halogen succinimide in the presence of TEMPO allows insertion reaction by an isocyanide, the product of which can further accept a wide range of nucleophiles for the generation of isothioureas and related molecular moieties. This new procedure overcomes previous methods that accept essentially only aryl amines as the third nucleophilic component. The diverse nucleophiles usable in our new protocol make this approach a general method for de novo synthesis of many S-containing heterocycles.
COA of Formula: C7H8O. About Benzyl Alcohol, If you have any questions, you can contact Lei, XF; Wang, YY; Fan, EK; Sun, ZH or concate me.
Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles