16525-35-2Relevant academic research and scientific papers
Decarboxylative thioamidation of arylacetic and cinnamic acids: A new approach to thioamides
Guntreddi, Tirumaleswararao,Vanjari, Rajeshwer,Singh, Krishna Nand
supporting information, p. 3624 - 3627 (2014/08/05)
A new decarboxylative strategy has been developed for the synthesis of thioamides via a three-component reaction involving arylacetic or cinnamic acids, amines and elemental sulfur powder, without the need of a transition metal and an external oxidant.
Three-component reaction between alkynes, elemental sulfur, and aliphatic amines: A general, straightforward, and atom economical approach to thioamides
Nguyen, Thanh Binh,Tran, Minh Quan,Ermolenko, Ludmila,Al-Mourabit, Ali
supporting information, p. 310 - 313 (2014/01/23)
A general, straightforward, and atom-economical three-component synthesis of thioamides from alkynes, elemental sulfur, and aliphatic amines has been developed.
Synthesis of thioamides via one-pot A3-coupling of alkynyl bromides, amines, and sodium sulfide
Sun, Yadong,Jiang, Huanfeng,Wu, Wanqing,Zeng, Wei,Li, Jianxiao
supporting information, p. 700 - 707 (2014/01/06)
We herein describe a novel method for the synthesis of thioamides by a three component condensation of alkynyl bromides, amines, and Na 2S·9H2O. The developed method is applicable for a wide range of amines and alkynyl bromides bearing different functional groups furnishing the corresponding products in moderate to excellent yields. The Royal Society of Chemistry.
