摘要
The nucleophilic reaction of diamines and carbon disulfide in aqueous NaOH afforded a series of bis-dithiocarbamate salts. Activation of these with aqueous ClCH(2)COOK and subsequent nucleophilic substitution reaction with trisulfonamide aqueous KOH at room temperature provided N-tosyl-macrocycles containing two thiourea units. This strategy has the advantages of simple operation, mild reaction condition, easy product-isolation and environmental friendliness.
- 出版日期2010
- 单位天津大学