Reactivity of 4H-3,1-benzoxazin-4-ones towards nitrogen and carbon nucleophilic reagents: Applications to the synthesis of new heterocycles

Arkivoc

Volumn 2004, Issue 1, 2004, Pages 36-54

  Madkour, H M F ^a  

^a Ain Shams University   (Egypt)

Author keywords

Benzoxazinones; Quinazolinones and Cyanoquinoline

Indexed keywords

1 HYDROXY 1 (2 ACETYLAMINO 3,5 DIBROMOPHENYL)METHYLIDENEBARBITURIC ACID; 1 HYDROXY 1 (2 ACETYLAMINO 3,5 DIBROMOPHENYL)METHYLIDENETHIOBARBITURIC ACID; 1,2 PHENYLENEDIAMINE; 10 BROMO 6 ISOPROPYL 2 OXO 3H,4H 1,2,4 TRIAZINO[2,3 C]QUINAZOLINE; 2 ACETYLAMINO 3,5 DIBROMO 2',4'(5') DIMETHYLBENZOPHENONE; 2 ACETYLAMINO 3,5 DIBROMO 4' ETHYLBENZOPHENONE; 2 ACETYLAMINO 3,5 DIBROMOBENZOPHENONE; 3 (2 AMINOPHENYL) 6,8 DIBROMO 2 METHYL 4(3H) QUINAZOLINONE; 3 (4 ACETOPHENYL) 6,8 DIBROMO 2 METHYL 4(3H) QUINAZOLINONE; 3 ACETOXY 6,8 DIBROMO 2 METHYL 4(3H) QUINAZOLINONE; 3,5 DIBROMO 2 (1 HYDROXY 1 PHENYL)ETHYLAMINOBENZOPHENONE; 4H 3,1 BENZOXAZIN 4 ONE DERIVATIVE; 6 BROMO (4H) 3,1 BENZOXAXIN 4 ONE; 6 BROMO 3 [2 (4 CHLOROPHENYL) 4 OXO 1,3 THIAZOL 3 YL] 2 ISOPROPYL 4(3H) QUINAZOLINONE; 6,8 DIBROMO (4H) 3,1 BENZOXAZINONE; 6,8 DIBROMO 2 METHYL 3 (4 SULFONAMIDOPHENYL) 4(3H) QUINAZOLINONE; 6,8 DIBROMO 3 (2 HYDROXYETHYL) 2 METHYL 4(3H) QUINAZOLINONE; 6,8 DIBROMO 3 (N PHTHALIMIDOETHYL) 2 METHYL 4(3H) QUINAZOLINONE; 6,8 DIBROMO 3 ETHOXYCARBONYLMETHOXY 2 METHYL 4(3H) QUINAZOLINONE; 6,8 DIBROMO 3 HYDROXY 2 METHYL 4(3H) QUINAZOLINONE; 7,9 DIBROMO 2 OXO 3 PHENYL 4 [PHENYLAMINOCARBONYL]IMINO 1,3 OXAZINO[5,6 C]QUINOLINE; 7,9 DIBROMO 5 METHYL 2 OXO 1,2,4 TRIAZOLO[2,3 C]QUINAZOLINE; [(2 HYDROXY 1 NAPHTHYL)ETHYL] 2 METHYL 4(3H) QUINAZOLINONE; [4 N (5 METHYL 3 ISOXAZOLYL)SULFONAMIDOPHENYL] 4(3H) QUINAZOLINONE; BENZYL 3,5 DIBROMO 2 (1 HYDROXY 1 BENZYL)ETHYLAMINOPHENYL KETONE; HETEROCYCLIC COMPOUND; HYDROXYLAMINE; REAGENT; SULFAMETHOXAZOLE; SULFANILAMIDE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL STRUCTURE; DRUG SYNTHESIS; FRIEDEL CRAFTS REACTION; REACTION ANALYSIS;

EID: 2942679380     PISSN: 14246376     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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