82044-09-5Relevant academic research and scientific papers
A One-Pot Process for the Enantioselective Synthesis of Amines via Reductive Amination under Transfer Hydrogenation Conditions
Williams, Glynn D.,Pike, Richard A.,Wade, Charles E.,Wills, Martin
, p. 4227 - 4230 (2007/10/03)
(Equation presented) Cyclic amines may be prepared via a sequence of deprotection followed by intramolecular reductive amination of t-Boc-protected amino ketones under asymmetric transfer hydrogenation conditions. In cases where the corresponding imine reaction proceeds with high enantioselectivity, this is reflected in the one-step process.
Reaction of Isoquinoline Enamides with Electrophiles
Lenz, George R.,Woo, Chi-Min,Hawkins, Bruce L.
, p. 3049 - 3053 (2007/10/02)
The reaction of isoquinoline enamides with acyl isocyanates yields vinylogous amides through carbon-carbon bond formation between the β carbon of the enamide and the isocyanate carbonyl.Enamide formation occurs between 1-benzyl-3,4-dihydroisoquinolines and phenylacetic anhydride.However, a N,C-bis(phenylacetyl) derivative is formed with phenylacetyl chloride.The reaction occurs through preferential reaction of phenylketene with the enamine tautomer of the 1-benzyl-3,4-dihydroisoquinoline at the carbon terminus, followed by N-acylation.The equilibrium is demonstrated by deuterium NMR.
