1244737-85-6Relevant articles and documents
An Ugi Reaction Incorporating a Redox-Neutral Amine C-H Functionalization Step
Zhu, Zhengbo,Seidel, Daniel
, p. 631 - 633 (2016)
Pyrrolidine and 1,2,3,4-tetrahydroisoquinoline (THIQ) undergo redox-neutral α-amidation with concurrent N-alkylation upon reaction with aromatic aldehydes and isocyanides. Reactions are promoted by acetic acid and represent a new variant of the Ugi reacti
Convenient synthesis of 1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid derivatives via isocyanide-based, three-component reactions
Schuster, Ildiko,Lazar, Laszlo,Fueloep, Ferenc
experimental part, p. 2488 - 2498 (2010/09/08)
The three-component reactions of 3,4-dihydroisoquinolines, isocyanides, and benzyl chloroformate furnished 2-benzyloxycarbonyl-1,2,3,4- tetrahydroisoquinoline-1-carboxamides in moderate to good yields. Hydrogenolysis or selective hydrolysis of the benzylo