Synthesis of new tetraheterocyclic systems by the mixed condensation reactions on [1,2,4]triazolo[4,3-a][1,5]benzodiazepines

Synthetic Communications

Volumn 36, Issue 5, 2006, Pages 573-578

  Boudina, A ^a   Baouid, A ^a,b   Hasnaoui, A ^a   Essaber, M ^a  

^a FACULTÉ DES SCIENCES SEMLALIA   (Morocco)

^b CADI AYYAD UNIVERSITY   (Morocco)

Author keywords

Benzodiazepine; Bis adducts; Nitrile oxides; Nitrilimines; Oxadiazole; Regioselective; Triazole

Indexed keywords

BENZODIAZEPINE DERIVATIVE; CARBOXYLIC ACID DERIVATIVE; ETHYL 1 (4 CHLOROPHENYL) 4A METHYL 5 (4 NITROPHENYL) 3A PHENYL 3A,4A,8,13 TETRAHYDRO 4H [1,2,4]OXADIAZOLO[5,4 D][1,2,4]TRIAZOLO[4,3 A][1,5]BENZODIAZEPINE 7 CARBOXYLATE; ETHYL 1,5 BIS(4 CHLOROPHENYL) 4A METHYL 3A PHENYL 3A,4A,8,13 TETRAHYDRO 4H BIS[1,2,4]OXADIAZOLO[5,4 D][1,2,4]TRIAZOLO[4,3 A][1,5]BENZODIAZEPINE 7 CARBOXYLATE; ETHYL 3 (4 CHLOROPHENYL) 3A METHYL 4A,5 DIPHENYL 7 (4 TOLYL) 3A,4A,8,13 TETRAHYDRO 4H BIS[1,2,4 TRIAZOLO][4,3 A:3',4' D][1,5]BENZODIAZEPINE 1 CARBOXYLATE; ETHYL 3 (4 CHLOROPHENYL) 3A METHYL 7 (4 NITROPHENYL) 4A,5 DIPHENYL 3A,4A,8,13 TETRAHYDRO 4H BIS[1,2,4 TRIAZOLO][4,3 A:3',4' D][1,5]BENZODIAZEPINE 1 CARBOXYLATE; ETHYL 3,7 BIS(4 CHLOROPHENYL) 3A METHYL 4A,5 DIPHENYL 3A,4A,8,13 TETRAHYDRO 4H BIS[1,2,4 TRIAZOLO][4,3 A:3',4' D][1,5]BENZODIAZEPINE 1 CARBOXYLATE; ETHYL 3A METHYL 3 (4 NITROPHENYL) 4A,5 DIPHENYL 7 (4 TOLYL) 3A,4A,8,13 TETRAHYDRO 4H BIS[1,2,4 TRIAZOLO][4,3 A:3',4' D][1,5]BENZODIAZEPINE 1 CARBOXYLATE; ETHYL 4A METHYL 1,5 DI(4 CHLOROPHENYL) 3A METHYL 3A PHENYL 3A,4A,8,13 TETRAHYDRO 4H [1,2,4]OXADIAZOLO[5,4 D][1,2,4]TRIAZOLO[4,3 A][1,5]BENZODIAZEPINE 7 CARBOXYLATE; ETHYL 7 (4 NITROPHENYL) 3A METHYL 3 (4 NITROPHENYL) 4A,5 DIPHENYL 3A,4A,8,13 TETRAHYDRO 4H BIS[1,2,4 TRIAZOLO][4,3 A:3',4' D][1,5]BENZODIAZEPINE 1 CARBOXYLATE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL PROCEDURES; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLOADDITION; MASS SPECTROMETRY; POLYMERIZATION; PROTON NUCLEAR MAGNETIC RESONANCE;

EID: 32644481377     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910500406443     Document Type: Article

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