853995-38-7Relevant articles and documents
Synthesis of N,N-disubstituted 3-amino-1,4-diynes and 3-amino-1-ynes by addition of alkynyldimethylaluminum reagents to N,N-disubstituted formamides and N,O-acetals
Korbad, Balaji L.,Lee, Sang-Hyeup
, p. 5089 - 5095 (2014/08/18)
A wide range of alkynyldimethylaluminum reagents, which were derived from terminal alkynes and trimethylaluminum, underwent a double addition to N,N-disubstituted formamides and their acetals to provide the corresponding N,N-disubstituted 3-amino-1,4-diynes in moderate to excellent yields. Also, these reagents smoothly underwent the addition to N,O-acetals to give the corresponding N,N-disubstituted 3-amino-1-ynes in excellent yields.
Addition reaction of zinc acetylides to thioiminium salts leading to 3-amino-1-sulfenyl-1,4-enynes
Murai, Toshiaki,Ohta, Yukiyasu,Mutoh, Yuichiro
, p. 3637 - 3640 (2007/10/03)
The reaction of thioiminium salts with zinc acetylides took place at 60°C to give 3-amino-1-sulfenyl-1,4-enynes in moderate to good yields. Two molecules of acetylides were incorporated into the products. Nucleophilic attack of zinc acetylides to thioimin