10549-16-3Relevant articles and documents
Synthesis of Polycyclic Imidazolidinones via Amine Redox-Annulation
Zhu, Zhengbo,Lv, Xin,Anesini, Jason E.,Seidel, Daniel
, p. 6424 - 6427 (2017)
α-Ketoamides undergo redox-annulations with cyclic secondary amines, such as 1,2,3,4-tetrahydroisoquinoline, pyrrolidine, piperidine, and morpholine. Catalytic amounts of benzoic acid significantly accelerate these transformations. This approach provides
ASYMMETRIC CATALYTIC HYDROGENATIONS OF CHIRAL alpha -KETO AMIDES.
Harada,Munegumi
, p. 3203 - 3209 (2007/10/02)
Asymmetric catalytic hydrogenations of chiral pyruvamides were carried out using palladium on charcoal (Pd-C) as a catalyst to give lactamides with the diastereoisomeric purities (d. p. ) of up to 62%. It was found that there was a linear correlation betw