1613243-68-7

Upstream product

• 1613244-01-1 (S)-1-(3,4-dihydroquinolin-1(2H)-yl)-2-(piperidin-1-yl)propan-1-one 
• 4392-24-9 Cinnamyl bromide 
• 4392-24-9 3-bromo-1-phenyl-1-propenyl bromide 
• 1217715-96-2 (S)-2-amino-1-(3,4-dihydroquinolin-1(2H)-yl)propan-1-one 
• 1613243-98-3 (S)-benzyl (1-(3,4-dihydroquinolin-1(2H)-yl)-1-oxopropan-2-yl)carbamate 

Relevant academic research and scientific papers

Double axial chirality promoted asymmetric [2,3] Stevens rearrangement of N-cinnamyl l-alanine amide-derived ammonium ylides

The base-induced asymmetric [2,3] Stevens rearrangement of N-cinnamyl tetraalkylammonium ylides derived from l-alanine amides proceeds via a double axially chiral intermediate to afford the corresponding α-substituted alanine derivatives with high enantio- and diastereoselectivities. the Partner Organisations 2014.