Palladium-catalysed direct arylation of heteroaromatics using unprotected iodoanilines with inhibition of the amination reaction

Synthesis (Germany)

Volumn 44, Issue 14, 2012, Pages 2264-2276

  Beladhria, Anissa ^a,b,c   Beydoun, Kassem ^b   Ammar, Hamed Ben ^a   Salem, Ridha Ben ^c   Doucet, Henri ^b  

^a UNIVERSITY OF GABES   (Tunisia)

^b UMR 6509 Organometalliques et Catalyse Chimie et Electrochimie Moleculaires   (France)

^c UNIVERSITY OF SFAX   (Tunisia)

Author keywords

amines; catalysis; green chemistry; heterocycles; palladium

Indexed keywords

AMINATION REACTION; ARYLATIONS; GREEN CHEMISTRY; HETEROARENES; HETEROAROMATICS; HETEROCYCLES; HIGH YIELD; POTASSIUM ACETATE;

AMINES; AROMATIC COMPOUNDS; PALLADIUM;

CATALYSIS;

1 [5 (2 AMINOPHENYL) 4 CHLOROTHIOPHEN 2 YL]ETHANONE; 1 [5 (3 AMINOPHENYL) 1 METHYLPYRROL 2 YL]ETHANONE; 1 [5 (3 AMINOPHENYL) 4 CHLOROTHIOPHEN 2 YL]ETHANONE; 1 [5 (3 AMINOPHENYL) 4 METHYLTHIOPHEN 2 YL]ETHANONE; 1 [5 (4 AMINOPHENYL) 4 CHLOROTHIOPHEN 2 YL]ETHANONE; 2 (2 ISOBUTYLTHIAZOL 5 YL)PHENYLAMINE; 3 (1 METHYLPYRROL 2 YL)PHENYLAMINE; 3 (2 ISOBUTYLTHIAZOL 5 YL)PHENYLAMINE; 3 (2 PROPYLTHIAZOL 5 YL)PHENYLAMINE; 3 (3,5 DIMETHYLISOXAZOL 4 YL)PHENYLAMINE; 3 (5 BUTYLTHIOPHEN 2 YL)PHENYLAMINE; 3 (5 CHLOROTHIOPHEN 2 YL)PHENYLAMINE; 3 (5 METHYLTHIOPHEN 2 YL)PHENYLAMINE; 3 (5 NUTYLFURAN 2 YL)PHENYLAMINE; 3 [5 (2 METHYL[1,3]DIOXOLAN 2 YL)THIOPHEN 2 YL]PHENYLAMINE; 4 (1 METHYLPYRROL 2 YL)PHENYLAMINE; 4 (2 ISOBUTYLTHIAZOL 5 YL)PHENYLAMINE; 4 (2 PROPYLTHIAZOL 5 YL)PHENYLAMINE; 4 (5 IBUTYLTHIOPHEN 2 YL) 2 CHLOROPHENYLAMINE; 5 (2 AMINOPHENYL)THIOPHENE 2 CARBONITRILE; 5 (3 AMINOPHENYL)THIOPHENE 2 CARBONITRILE; 5 (4 AMINO 3 CHLOROPHENYL)THIOPHENE 2 CARBONITRILE; 5 (4 AMINOPHENYL)THIOPHENE 2 CARBONITRILE; ACETIC ACID; ANILINE DERIVATIVE; AROMATIC AMINE; IODOANILINE DERIVATIVE; METHYL 5 (3 AMINOHENYL) 2 METHYLFURAN 3 CARBOXYLATE; PALLADIUM; UNCLASSIFIED DRUG; UNINDEXED DRUG;

AMINATION; ARTICLE; ARYLATION; CATALYSIS; DRUG STRUCTURE; DRUG SYNTHESIS; ENZYME INHIBITION;

EID: 84863724841     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0031-1291124     Document Type: Article

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