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Volumn 60, Issue 44, 2004, Pages 9937-9944
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Synthesis of indazole-N-oxides via the 1,7-electrocyclization of azomethine ylides
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Author keywords
Cycloadditions; Electrocyclic reactions; Indazoles; Isoquinolines; Nitro compounds
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Indexed keywords
2 BENZYL 2H INDAZOLE N OXIDE;
2 METHYL 2H INDAZOLE;
2 METHYL 2H INDAZOLE N OXIDE;
2 METHYL 5 BROMO 2H INDAZOLE N OXIDE;
2 METHYL 5,6 DIMETHOXY 2H INDAZOLE N OXIDE;
2 METHYL 5,6 METHYLENEDIOXY 2H INDAZOLE N OXIDE;
2,3 DIMETHOXY 8 (2 NITROPHENYL) 10 PHENYL 8,8A,11A,11B TETRAHYDRO 6H PYRROLO[3'4':3,4]PYRROLO[2,1 A]ISOQUINOLINE 9,11(5H,10H) DIONE;
3 BENZYL 5 (2 NITROPHENYL)OXAZOLIDINE;
3 METHYL 5 (2' NITROPHENYL)OXAZOLIDINE;
3 METHYL 5 (3' BROMO 6' NITROPHENYL)OXAZOLIDINE;
3 METHYL 5 (3',4' DIMETHOXY 6' NITROPHENYL)OXAZOLIDINE;
3 METHYL 5 (3',4' METHYLENEDIOXY 6' NITROPHENYL)OXAZOLIDINE;
4,5 DIMETHOXY 2 [2' (2''H 2'' INDAZOLYL 1'' N OXIDE)ETHYL]BENZALDEHYDE;
6,7 DIETHOXY 1 (2' NITROPHENYL) 3,4 DIHYDROISOQUINOLINE;
6,7 DIETHOXY 1 (5' CHLORO 2' NITROPHENYL) 3,4 HYDROISOQUINOLINE;
6,7 DIMETHOXY 1 (2' NITROPHENYL) 3,4 DIHYDROISOQUINOLINE;
6,7 DIMETHOXY 1 (5' CHLORO 2' NITROPHENYL) 3,4 DIHYDROISOQUINOLINE;
AZOMETHINE YLIDE;
INDAZOLE DERIVATIVE;
UNCLASSIFIED DRUG;
ANALYTIC METHOD;
ARTICLE;
CHEMICAL REACTION;
CHEMICAL STRUCTURE;
CYCLIZATION;
DRUG SYNTHESIS;
PRIORITY JOURNAL;
REACTION ANALYSIS;
STRUCTURE ANALYSIS;
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EID: 4644281548
PISSN: 00404020
EISSN: None
Source Type: Journal
DOI: 10.1016/j.tet.2004.08.026 Document Type: Article |
Times cited : (25)
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References (14)
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