14429-15-3Relevant articles and documents
Br?nsted acid catalyzed reductive amination with benzothiazoline as a highly efficient hydrogen donor
Zhu, Chen,Akiyama, Takahiko
, p. 1251 - 1254 (2011)
Reductive amination of aldehyde and amine proceeded smoothly in the presence of benzothiazoline as efficient hydrogen source by means of 20 mol% trifluoroacetic acid to give the corresponding amines in excellent yields. Hydrogen-donor abilities of benzothiazoline, benzimidazoline, and benzoxazoline were compared. Georg Thieme Verlag Stuttgart - New York.
Molecular iodine catalyzed transfer hydrogenation: Reduction of aldimines, ketimines, and α-imino esters
Bachu, Prabhakar,Zhu, Chen,Akiyama, Takahiko
supporting information, p. 3977 - 3981 (2013/07/25)
An efficient and practical protocol for the reduction of aldimines, ketimines, and α-imino esters in the presence of catalytic amount of molecular iodine with Hantzsch ester at ambient temperature afforded the corresponding amines in excellent yields.