Domino-Heck reactions of carba- and oxabicyclic, unsaturated dicarboximides: Synthesis of aryl-substituted, bridged perhydroisoindole derivatives

Helvetica Chimica Acta

Volumn 92, Issue 6, 2009, Pages 1092-1101

  Celik, Cumali ^a   Kulu, Irem ^a   Ocal, Nuket ^a   Kaufmann, Dieter E ^b  

^a YILDIZ TECHNICAL UNIVERSITY   (Turkey)

^b CLAUSTHAL UNIVERSITY OF TECHNOLOGY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

C-C COUPLING; C-C COUPLING REACTIONS; HECK ARYLATION; HECK REACTIONS; TRIMETHYLSILYL;

ACETYLENE; AMINES; CHEMICAL REACTIONS; LIGHTING;

AROMATIC COMPOUNDS;

5 (4 CHLOROPHENYL) N (4 METHOXYPHENYL) 6 EXO (PHENYLETHYNYL) 7 OXABICYCLO[2.2.1]HEPTANE 2 EXO,3 EXO DICARBOXIMIDE 5 (4 CHLOROPHENYL)HEXAHYDRO 2 4 METHOXYPHENYL 6 (2 PHENYLETHYNYL) 4,7 EPOXY 1H ISOINDOLE 1,3(2H) DIONE; 5 EXO (4 CHLOROPHENYL) N PHENYL 6 EXO (2 PHENYLETHYNYL) 7 OXABICYCLO[2.2.1]HEPTANE 2 EXO,3 EXO DICARBOXIMIDE 5 (4 CHLOROPHENYL)HEXAHYDRO 2 PHENYL 6 (2 PHENYLETHYNYL) 4,7 EPOXY 1H ISOINDOLE 1,3(2H) DIONE; 5 EXO (4 CHLOROPHENYL) N PHENYL EXO [2 (6 TRIMETHYLSILYL)ETHYNYL] 7 OXABICYCLO[2.2.1]HEPTANE 2 EXO,3 EXO DICARBOXIMIDE 5 (4 CHLOROPHENYL)HEXAHYDRO 2 PHENYL 6 [2 (TRIMETHYLSILYL)ETHYNYL] 4,7 EPOXY 1H ISOINDOLE 1,3(2H) DIONE; 5 EXO (4 METHOXYPHENYL) N PHENYL 6 EXO [2 (TRIMETHYLSILYL)ETHYNYL] 7 OXABICYCLO[2.2.1]HEPTANE 2 EXO,3 EXO DICARBOXIMIDE HEXAHYDRO 5 (4 METHOXYPHENYL) 2 PHENYL 6 [2 (TRIMETHYLSILYL)ETHYNYL] 4,7 EPOXY 1H ISOINDOLE 1,3(2H) DIONE; 5 EXO (6 CHLOROPYRIDIN 3 YL) N (4 METHOXYPHENYL) 7 OXABICYCLO[2.2.1]HEPTANE 2 EXO,3 EXO DICARBOXIMIDE 5 (6 CHLOROPYRIDIN 3 YL)HEXAHYDRO 2 (4 METHOXYPHENYL) 4,7 EPOXY 1H ISOINDOLE 1,3(2H) DIONE; 5 HYDROXY 4 (4 METHOXYPHENYL) 8 'EXO' (NAPHTHALEN 1 YL) 10 OXA 4 AZATRICYCLO[5.2.1.02,6]DECAN 3 ONE OCTAHYDRO 3 HYDROXY 2 (4 METHOXYPHENYL) 5 (NAPHTHALEN 1 YL) 4,7 EPOXY 1H INDOL 1 ONE; 5 HYDROXY 4 (4 METHOXYPHENYL) 9 'EXO' (NAPHTHALEN 1 YL) 10 OXA 4 AZATRICYCLO[5.2.1.0 2,6]DECAN 3 ONE OCTAHYDRO 3 HYDROXY 2 (4 METHOXYPHENYL) 6 (NAPHTHALEN 1 YL) 4,7 EPOXY 1H INDOL 1 ONE; 8 'EXO' (NAPHTHALEN 1 YL) 4 PHENYL 10 OXA 4 AZATRICYCLO[5.2.1.0 2,6]DECANE OCTAHYDRO 5 (NAPHTHALEN 1 YL) 2 PHENYL 4,7 EPOXY 1H ISOINDOLE; ISOINDOLE DERIVATIVE; N (4 CHLOROPHENYL) 5 EXO (NAPHTHALEN 1 YL) 7 OXABICYCLO[2.2.1]HEPTANE 2 EXO,3 EXO DICARBOXIMIDE 2 (4 CHLOROPHENYL)HEXAHYDRO 5 (NAPHTHALEN 1 YL) 4,7 EPOXY 1H ISOINDOLE 1,3(2H) DIONE; N (4 CHLOROPHENYL) 5 EXO PHENYL 6 EXO [2 (TRIMETHYLSILYL)ETHYNYL] 7 OXABICYCLO[2.2.1]HEPTANE 2 EXO,3 EXO DICARBOXIMIDE 2 (4 CHLOROPHENYL)HEXAHYDRO 5 PHENYL 6 [2 (TRIMETHYLSILYL)ETHYNYL] 4,7 EPOXY 1H ISOINDOLE 1,3(2H) DIONE; N (4 METHOXYPHENYL) 5 EXO (2 THIENYL) 7 OXABICYCLO[2.2.1]HEPTANE 2 EXO,3 EXO DICARBOXIMIDE HEXAHYDRO 2 (4 METHOXYPHENYL) 5 (2 THIENYL) 4,7 EPOXY 1H ISOINDOLE 1,3(2H) DIONE; N (4 METHOXYPHENYL) 5 EXO PHENYL 7 OXABICYCLO[2.2.1]HEPTANE 2 EXO,3 EXO DICARBOXIMIDE HEXAHYDRO 2 (4 METHOXYPHENYL) 5 PHENYL 4,7 EPOXY 1H ISOINDOLE 1,3(2H) DIONE; N,5 EXO BIS(4 CHLOROPHENYL) 7 OXABICYCLO[2.2.1]HEPTANE 2 EXO,3 EXO DICARBOXIMIDE 2,5 BIS(4 CHLOROPHENYL)HEXAHYDRO 4,7 EPOXY 1H ISOINDOLE 1,3(2H) DIONE; UNCLASSIFIED DRUG;

ARTICLE; ARYLATION; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYSIS; CHEMICAL STRUCTURE; HECK REACTION; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS;

EID: 67649669767     PISSN: 0018019X     EISSN: None     Source Type: Journal    
DOI: 10.1002/hlca.200800388     Document Type: Article

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