100342-54-9

Upstream product

• 90097-61-3 2-acetylamino-2-ethoxycarbonyl-3-<2(1H)-quinolinon-4-yl>propionate 
• 100-46-9 benzylamine 
• 21298-80-6 2-(2-oxo-1,2-dihydroquinoline-4-yl)acetic acid 
• 103702-23-4 (2-oxo-1,2-dihydroquinolin-4-yl)acetic acid methylester 
• 607-66-9 4-methyl-1,2-dihydroquinolin-2-one 
• 5322-08-7 4-(2-hydroxyethyl)quinolin-2-(1H)-one 

Downstream Products

• 831176-43-3 N-benzyl-N-[2-(2-oxo-1,2-dihydro-4-quinolyl)ethyl]acrylamide 
• 831176-44-4 N-benzyl-2-methyl-N-[2-(2-oxo-1,2-dihydro-4-quinolyl)ethyl]acrylamide 
• 906664-09-3 N-benzyl-2-ethyl-N-[2-(2-oxo-1,2-dihydro-4-quinolyl)ethyl]acrylamide 

Relevant academic research and scientific papers

Stereoselective intra- and intermolecular [2+2] photocycloaddition reactions of 4-(2′-aminoethyl)quinolones

The 4-(2′-aminoethyl)quinolones 6, 8 and 9 were prepared starting from 4-(2′-bromoethyl)quinolone (4) in two steps and overall yields of 56-93%. They underwent inter- and intramolecular [2+2] photocycloaddition reactions with an alkene to provide the cycl

Photochemistry of 4-(2′-aminoethyl)quinolones: Enantioselective synthesis of tetracyclic tetrahydro-1aH-pyrido[4′,3′:2,3]- cyclobuta[1,2-c] quinoline-2,11(3H,8H)-diones by intra- and intermolecular [2 + 2]-photocycloaddition reactions in solution

Enantioselective [2 + 2]-photocycloaddition reactions on 4-(2′-aminoethyl)quinolones in solution were studied using the enantiomerically pure complexing agent 1 as source of chirality. The intermolecular reactions of fully N-protected substrates 5a-5c wit