Ring transformations of 2,3-dihydroisoxazoles via azomethine ylides - Formation of annulated 5- and 7-membered N-heterocycles

Tetrahedron

Volumn 57, Issue 20, 2001, Pages 4349-4358

  Friebolin, Wolfgang ^a   Eberbach, Wolfgang ^a  

^a UNIVERSITY OF FREIBURG   (Germany)

Author keywords

2,3 dihydroisoxazoles; Azepines; Azomethine ylides; Dipolar cyclizations

Indexed keywords

1 (10A METHYL 1,2,3,4,10,10A HEXAHYDROPYRIDO[1,2 A]AZEPIN 6 YL) 2,2 DIMETHYLPROPAN 1 ONE; 1 (2,2 DIMETHYL 7 VINYL 2,3 DIHYDRO 1H PYRROLIZIN 5 YL) 2,2 DIMETHYLPROPAN 1 ONE; 1 (2,2,9A TRIMETHYL 2,3,9,9A TETRAHYDRO 1H PYRROLO[1,2 A]AZEPIN 5 YL) 2,2 DIMETHYLPROPAN 1 ONE; 2,2 DIMETHYL 1 (1 VINYL 5,6,7,8 TETRAHYDROINDOLIZIN 3 YL)PROPAN 1 ONE; 2,3 DIHYDROISOXAZOLE DERIVATIVE; 3 [BUTA 1,3 DIENYL] 2 (TERT BUTYL) 3A METHYL 4,5,6,7 TETRAHYDRO 3AH ISOXAZOLO[2,3 A]PYRIDINE; 3 [BUTA 1,3 DIENYL] 2 (TERT BUTYL) 3A,5,5 TRIMETHYL 3A,4,5,6 TETRAHYDROPYRROLO[1,2 B]ISOXAZOLE; 3 [BUTA 1,3 DIENYL] 2 (TERT BUTYL) 3A,6,6 TRIMETHYL 3A,4,5,6 TETRAHYDROPYRROLO[1,2 B]ISOXAZOLE; 3 [BUTA 1,3 DIENYL] 2 PHENYL 3A,5,5 TRIMETHYL 3A,4,5,6 TETRAHYDROPYRROLO[1,2 B]ISOXAZOLE; 3 [BUTA 1,3 DIENYL] 3A METHYL 2 PHENYL 4,5,6,7 TETRAHYDRO 3AH ISOXAZOLO[2,3 A]PYRIDINE; 3 [BUTA 1,3 DIENYL] 3A,6,6 TRIMETHYL 2 PHENYL 3A,4,5,6 TETRAHYDROPYRROLO[1,2 B]ISOXAZOLE; AZEPINE DERIVATIVE; AZOMETHINE YLIDE; DIHYDROAZEPINE DERIVATIVE; ISOXAZOLE DERIVATIVE; PHENYL (1 VINYL 4,5,6,7 TETRAHYDROINDOLIZIN 3 YL)METHANONE; PHENYL (10A METHYL 1,2,3,4,10,10A HEXAHYDROPYRIDO[1,2 A]AZEPIN 6 YL)METHANONE; PHENYL (2,2,9A TRIMETHYL 2,3,9,9A TETRAHYDRO 1H PYRROLO[1,2 A]AZEPIN 5 YL)METHANONE; PHENYL (3,3,9A TRIMETHYL 2,3,9,9A TETRAHYDRO 1H PYRROLO[1,2 A]AZEPIN 5 YL)METHANONE; PHENYL (5,5 DIMETHYL 1 VINYL 6,7 DIHYDRO 5H PYRROLIZIN 3 YL)METHANONE; PHENYL (6,6 DIMETHYL 1 VINYL 6,7 DIHYDRO 5H PYRROLIZIN 3 YL)METHANONE; PYRROLE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL MODIFICATION; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLIZATION; PRIORITY JOURNAL; REACTION ANALYSIS; STRUCTURE ANALYSIS;

EID: 0035858655     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(01)00322-2     Document Type: Article

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