120154-96-3

Usage

InChI:InChI=1/C24H12N4/c1-3-7-17-13(5-1)15-9-11-25-21-19(15)23(27-17)24-20-16(10-12-26-22(20)21)14-6-2-4-8-18(14)28-24/h1-12H

Upstream product

• 150127-43-8 9-methyl-8H-acridino<2,3,4-de><3,6>phenanthrolin-8-one 
• 1188-33-6 N,N-dimethylformamide diethyl diacetal 
• 120-80-9 benzene-1,2-diol 
• 14428-46-7 9-methyl-3,4-dihydroacridin-1(2H)-one 
• 148149-00-2 N-(3-(2-aminophenyl)-3-oxopropyl)-2,2,2-trifluoroacetamide 
• 150127-36-9 2-trifluoromethanesulfonyl-5,8-dimethoxy-4-(2-nitrophenyl)quinoline 
• 150127-39-2 6-acetylanilino-4-(2-nitrophenyl)quinoline-5,8-dione 
• 150127-40-5 11-methy-4-(2-nitrophenyl)pyrido<2,3-b>acridine-5,12-dione 
• 150127-42-7 10-(2-acetylanilino)-8H-benzo<4,3,2-de><3,6>phenanthrolin-8-one 
• 121998-60-5 5,8-Dimethoxy-4-(2-nitrophenyl)-2(1H)-quinolinone 
• 150127-37-0 5,8-dimethoxy-4-(2-nitrophenyl)quinoline 
• 150127-38-1 4-(2-nitrophenyl)quinoline-5,8-dione 
• 114552-25-9 4-<2-(trifluoroacetylamino)phenyl>quinoline-5,8-dione 
• 551-93-9 2-aminoacetophenone 

Relevant academic research and scientific papers

A divergent approach to the total synthesis of the marine pyridoacridine alkaloid eilatin and its synthetic isomer isoeilatin

Herein we report the total synthesis of the heptacyclic pyridoacridine alkaloid eilatin (1) and its synthetic isomer isoeilatin (2). Starting from readily available 9-methyl-3,4-dihydroacridin-1(2H)-one (5) and 2-aminoacetophenone, a divergent synthesis gave alkaloid 1 in seven, and isomer 2 in eight steps.

A two step biomimetic total synthesis of eilatin

The symmetrical tetraaza heptacyclic alkaloid eilatin (1) was synthesized in a biomimetic two step reaction from catechol and monotrifluoro kynuramine (6) under oxidative conditions in the first step (aq. EtOH, NaIO3) and basic conditions (ammo

TOTAL SYNTHESIS OF EILATIN

Synthesis of the symmetrical pentacyclic fused aromatic alkaloid called eilatin (1) is described.