73683-05-3

Upstream product

• 100-39-0 benzyl bromide 
• 73683-04-2 ethyl N-(1,2-dihydro-2-oxo-1-qunolil)glycinate 
• 26539-38-8 1-amino-1,2-dihydroisoquinolin-2(1H)-one 

Downstream Products

• 73683-06-4 N-benzyl N-(1,2-dihydro-2-oxo-1-qunolil)glycin 
• 73683-06-4 [Benzyl-(2-oxo-2H-quinolin-1-yl)-amino]-acetic acid 
• 73683-06-4 [Benzyl-(2-oxo-2H-quinolin-1-yl)-amino]-acetic acid 
• 78034-54-5 [Benzyl-(2-oxo-2H-quinolin-1-yl)-amino]-acetic acid; compound with (S)-1-phenyl-ethylamine 
• 78034-56-7 (S)-(6-Methoxy-quinolin-4-yl)-((1S,2S,4S,5R)-5-vinyl-1-aza-bicyclo[2.2.2]oct-2-yl)-methanol; compound with [benzyl-(2-oxo-2H-quinolin-1-yl)-amino]-acetic acid 

Relevant academic research and scientific papers

Optical Activity as a Consequence of an N-N-Chiral Axis: Resolution of N-Benzyl-N-(1,2-Dihydro-2-oxo-1-quinolyl)glycine

The title compound (6) has been synthesised and the pure, laevorotatory enantiomer separated via the quinine salt.Rates of racemisation give a barrier for rotation around the N-N bond of 26 +/- 0.5 kcal mol-1.