39234-20-3Relevant articles and documents
Utilization of carbon disulfide as a powerful building block for the synthesis of 2-aminobenzoxazoles
Guntreddi, Tirumaleswararao,Allam, Bharat Kumar,Singh, Krishna Nand
, p. 9875 - 9880 (2013/09/02)
This protocol describes a novel, mild and convenient route to afford 2-aminobenzoxazoles in high yields, and represents a significant advance towards an environmentally friendly strategy. Aliphatic amines are made to react with carbon disulfide to provide intermediate dithiocarbamates (DTC), which in the presence of 2-aminophenol, subsequently undergo successive intermolecular nucleophilic attack and desulfurization to produce 2-aminobenzoxazoles within 3 h.
INVESTIGATION IN THE FIELD OF BIACETYLENE DERIVATIVES. XLII. ADDITION OF AMMONIUM DITHIOCARBAMATES TO BIACETYLENE
Sokolyanskaya, L. V.,Vavilova, A. N.,Volkov, A. N.,Trofimov, B. A.
, p. 2025 - 2028 (2007/10/02)
A simple method was developed for the production of cis-1-buten-ynyl dialkyldithiocarbamates and 1,4-bis(dialkylthiocarbamoylthio)-1,3-butadienes by the reaction of biacetylene and carbon bisulfide in the presence of secondary amines without a catalyst in protic and aprotic solvents.