62333-69-1

Upstream product

• 62497-65-8 4-nitro-N-phenethylbenzamide 
• 156-28-5 2-phenylethylamine hydrochloride 
• 122-04-3 4-nitro-benzoyl chloride 
• 64-04-0 phenethylamine 

Downstream Products

• 426840-05-3 4-(3,4-dihydro-[1]isoquinolyl)-aniline 
• 86448-89-7 1-(4-nitrophenyl)isoquinoline 
• 872788-13-1 7-nitro-1-(4-nitro-phenyl)-3,4-dihydro-isoquinoline 
• 88252-52-2 2-[9b-(4-Nitro-phenyl)-2-oxo-1,4,5,9b-tetrahydro-2H-azeto[2,1-a]isoquinolin-1-yl]-isoindole-1,3-dione 
• 92133-35-2 1-(4-Chloro-phenoxy)-9b-(4-nitro-phenyl)-1,4,5,9b-tetrahydro-azeto[2,1-a]isoquinolin-2-one 
• 86448-85-3 N-oxy p-nitrophenyl-1 dihydro-3,4 isoquinoleine 
• 877754-50-2 C₃₄H₂₆N₂O₄ 
• 86448-86-4 1-(4-nitrobenzoyl)indoline 
• 855653-41-7 7-nitro-1-(4-nitro-phenyl)-isoquinoline 
• 860370-44-1 5-nitro-1-(4-nitro-phenyl)-isoquinoline 
• 58992-84-0 4-(isoquinolin-1-yl)benzenamine 

Relevant academic research and scientific papers

Diprotonative stabilization of ring-opened carbocationic intermediates: conversion of tetrahydroisoquinoline to triarylmethanes

Superacid-promoted conversion of tetrahydroisoquinolines to triarylmethanes via tandem reactions of C-N bond scission, Friedel-Crafts alkylation, C-O bond scission, and electrophilic aromatic amidation was developed. Dication formation was important for stabilizing the ring-opened carbocationic intermediate, which is a new role for diprotonation in reaction mechanisms. This journal is

Asymmetric Transfer Hydrogenation of Unhindered and Non-Electron-Rich 1-Aryl Dihydroisoquinolines with High Enantioselectivity

The use of arene/Ru/TsDPEN catalysts bearing a heterocyclic group on the TsDPEN in the asymmetric transfer hydrogenation (ATH) of dihydroisoquinolines (DHIQs) containing meta- or para-substituted aromatic groups at the 1-position results in the formation of products of high enantiomeric excess. Previously, only 1-(ortho-substituted)aryl DHIQs, or with an electron-rich fused ring gave products with high enantioselectivity; therefore, this approach solves a long-standing challenge for imine ATH.

Highly-efficiency red-emitting platinum (II) complexes containing 4′-diarylamino-1-phenylisoquinoline ligands in polymer light-emitting diodes: Synthesis, structure, photoelectron and electroluminescence

Heteroleptic cyclometalated platinum (II) complexes bearing diarylamino-functionalized 1-phenylisoquinoline derivatives as primary ligand and acetyl acetonate as ancillary ligand were prepared and characterized. Single-crystal X-ray diffraction revealed t

(Dihydro) Isoquinoline derivatives as phosphodiesterase inhibitors

3,4-Dihydroisoquinoline and isoquinoline compounds of formula I, in which Ar represents a phenyl raidcal of the formulae IIa, IIb or IIc are novel effective PDE7 inhibitors.