Synthesis of isoindolo[2,1-a]quinazoline-5,11-dione derivatives via the reductive one-pot reaction of N-substituted 2-nitrobenzamides and 2-formylbenzoic acids

Helvetica Chimica Acta

Volumn 96, Issue 3, 2013, Pages 419-423

  Mahdavi, Mohammad ^a   Najafi, Ramin ^b   Saeedi, Mina ^a   Alipour, Eskandar ^b   Shafiee, Abbas ^a   Foroumadi, Alireza ^a  

^a TEHRAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^b ISLAMIC AZAD UNIVERSITY   (Iran)

Author keywords

Benzamides, 2 nitro ; Benzoic acids, 2 formyl ; Heterocycles; Isoindolo 2,1 a quinazoline 5,11 diones; Multicomponent reactions

Indexed keywords

2-NITROBENZAMIDES; BENZAMIDES; HETEROCYCLES; ISOINDOLO[2,1-A]QUINAZOLINE-5,11-DIONES; MULTI-COMPONENT REACTIONS; NUCLEOPHILIC ADDITIONS; ONE-POT REACTION; RING CLOSURES;

ADDITION REACTIONS;

SUBSTITUTION REACTIONS;

2 FORMYLBENZOIC ACID DERIVATIVE; 2 NITROBENZAMIDE DERIVATIVE; 6 (2 CHLOROBENZYL) 6,6A DIHYDROISOINDOL[2,1 A]QUINAZOLINE 5,11 DIONE; 6 (4 CHLOROBENZYL) 6,6A DIHYDRO 9, 10 DIMETHOXYISOINDOL[2,1 A]QUINAZOLINE 5,11 DIONE; 6 (4 CHLOROBENZYL) 6,6A DIHYDROISOINDOL[2,1 A]QUINAZOLINE 5,11 DIONE; 6 (FURAN 2 YLMETHYL) 6,6A DIHYDRO 9, 10 DIMETHOXYISOINDOL[2,1 A]QUINAZOLINE 5,11 DIONE; 6 (FURAN 2 YLMETHYL) 6,6A DIHYDROISOINDOL[2,1 A]QUINAZOLINE 5,11 DIONE; 6 BENZYL 6,6A DIHYDRO 9, 10 DIMETHOXYISOINDOL[2,1 A]QUINAZOLINE 5,11 DIONE; 6,6A DIHYDRO 6 (PYRIDIN 2 YLMETHYL)ISOINDOL[2,1 A]QUINAZOLINE 5,11 DIONE; 6,6A DIHYDRO 9, 10 DIMETHOXY 6 (PYRIDIN 2 YLMETHYL)ISOINDOL[2,1 A]QUINAZOLINE 5,11 DIONE; ALCOHOL; AMMONIA; BENZAMIDE DERIVATIVE; BENZOIC ACID DERIVATIVE; CARBOXYLIC ACID; FUNCTIONAL GROUP; ISOINDOL[2,1 A]QUINAZOLINE 5,11 DIONE DERIVATIVE; NUCLEOPHILE; QUINAZOLINE DERIVATIVE; STANNOUS CHLORIDE; UNCLASSIFIED DRUG;

ADDITION REACTION; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL BOND; DRUG STRUCTURE; DRUG SYNTHESIS; INFRARED SPECTROSCOPY; MASS SPECTROMETRY; ONE POT SYNTHESIS; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; REDUCTION;

EID: 84875232585     PISSN: 0018019X     EISSN: 15222675     Source Type: Journal    
DOI: 10.1002/hlca.201200199     Document Type: Article

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