92326-86-8Relevant articles and documents
Mild and Chemoselective Thioacylation of Amines Enabled by the Nucleophilic Activation of Elemental Sulfur
Saito, Masato,Murakami, Sho,Nanjo, Takeshi,Kobayashi, Yusuke,Takemoto, Yoshiji
supporting information, p. 8130 - 8135 (2020/05/20)
A mild and chemoselective method for the thioacylation of amines using α-keto acids and elemental sulfur has been developed. The key to the success of this transformation is the nucleophilic activation of elemental sulfur by thiols such as 1-dodecanethiol
1,2,3-Thiadiazoles. I. Synthesis of Sodium (or Potassium) 1,2,3-Thiadiazole-4-thiolates via Thiocarbazonate Esters and N-Acylthiohydrazonate Esters
Lee, Ving J.,Curran, William V.,Fields, Thomas F.,Learn, Keith
, p. 1873 - 1891 (2007/10/02)
A general synthesis of 1,2,3-thiadiazole-4-thiolates 1 and their derivatives 2-3 by an extension of the Hurd-Mori 1,2,3-thiadiazole synthesis is described.Treatment of methyl (or ethyl) hydrazinocarboxylates 11 (thiocarbazonate es