|
Volumn 64, Issue 19, 2008, Pages 4196-4203
|
Synthesis of dimethyl substituted benzimidazoles containing cyclopropane fused onto five to eight membered [1,2-a]alicyclic rings and influence of methyl group substituents on cytotoxicity of benzimidazolequinones
|
Author keywords
Antitumor agents; Aziridinylimines; Cycloaddition; Heterocycles
|
Indexed keywords
(1 ALLYL 5,6 DIMETHYL 1H BENZIMIDAZOL 2 YL) METHANOL;
(1 BUT 3 ENYL 5,6 DIMETHYL 1H BENZIMIDAZOL 2 YL)METHANOL;
(1 HEX 5 ENYL 5,6 DIMETHYL 1H BENZIMIDAZOL 2 YL)METHANOL;
(1 PENT 4 ENYL 5,6 DIMETHYL 1H BENZIMIDAZOL 2 YL)METHANOL;
1 ALLYL 5,6 DIMETHYL 1H BENZIMIDAZOLE 2 CARBALDEHYDE;
1 BUT 3 ENYL 5,6 DIMETHYL 1H BENZIMIDAZOLE 2 CARBALDEHYDE;
1 HEX 5 EN 1 YL 5,6 DIMETHYL 1H BENZIMIDAZOLE 2 CARBALDEHYDE;
1 PENT 4 EN 1 YL 5,6 DIMETHYL 1H BENZIMIDAZOLE 2 CARBALDEHYDE;
4,5 DIMETHYL 1,1A,8,8A TETRAHYDROCYCLOPROPA[3,4]PYRROLO[1,2 A]BENZIMIDAZOLE;
4,5 DIMETHYL 1,1A,8,8A TETRAHYDROCYCLOPROPA[3,4]PYRROLO[1,2 A]BENZIMIDAZOLE 3,6 DIONE;
4,5 DIMETHYLCYCLOPROPA[3,4]PYRROLO[1,2 A]BENZIMIDAZOLE 3,6 DIONE;
4,5 DIMETHYLCYCLOPROPAPYRROLO[1,2 A]BENZIMIDAZOLEQUINONE;
6,7 DIMETHYL 1A,2,3,9B TETRAHYDRO 1H CYCLOPROPA[3,4]PYRIDO[1,2 A]BENZIMIDAZOLE;
7,8 DIMETHYL 1,1A,3,4,10B HEXAHYDROCYCLOPROPA[3,4]AZEPINO[1,2 A]BENZIMIDAZOLE;
7,8 DIMETHYL 3,3A,4,10B TETRAHYDROPYRAZOLO[3',4':3,4]PYRROLO[1,2 A]BENZIMIDAZOLE;
8,9 DIMETHYL 1A,2,3,4,5,11B HEXAHYDRO 1H CYCLOPROPA[3,4]AZOCINO[1,2 A]BENZIMIDAZOLE;
ANTINEOPLASTIC AGENT;
BENZIMIDAZOLE DERIVATIVE;
BENZIMIDAZOLEQUINONE DERIVATIVE;
CARBENE;
CYCLOPROPANE;
CYCLOPROPAPYRROLOL[1,2 A]BENZIMIDAZOLEQUINONE;
HYDRAZONE DERIVATIVE;
N [(ALLYL 5,6 DIMETHYL 1H BENZIMIDAZOL 2 YL)METHYLENE] 2,3 DIPHENYLAZIRIDIN 1 AMINE;
N [(BUT 3 ENYL 5,6 DIMETHYL 1H BENZIMIDAZOL 2 YL)METHYLENE] 2,3 DIPHENYLAZIRIDIN 1 AMINE;
N [(HEX 5 ENYL 5,6 DIMETHYL 1H BENZIMIDAZOL 2 YL)METHYLENE] 2,3 DIPHENYLAZIRIDIN 1 AMINE;
N [(PENT 4 ENYL 5,6 DIMETHYL 1H BENZIMIDAZOL 2 YL)MEHYLENE] 2,3 DIPHENYLAZIRIDIN 1 AMINE;
UNCLASSIFIED DRUG;
ARTICLE;
CHEMICAL REACTION;
CONTROLLED STUDY;
CYCLOADDITION;
CYTOTOXICITY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
HUMAN;
HUMAN CELL;
PRIORITY JOURNAL;
SKIN FIBROBLAST;
|
EID: 41549123952
PISSN: 00404020
EISSN: None
Source Type: Journal
DOI: 10.1016/j.tet.2008.02.093 Document Type: Article |
Times cited : (19)
|
References (19)
|