Palladium-catalyzed synthesis of 2,3-disubstituted 5-azaindoles via heteroannulation reaction and of 2-substituted 5-azaindoles through domino sila-Sonogashira/5-endo cyclization

Journal of Organic Chemistry

Volumn 77, Issue 11, 2012, Pages 5006-5016

  Livecchi, Marion ^a,b,c   Calvet, Géraldine ^a,b   Schmidt, Frédéric ^a,b  

^a INSTITUT CURIE   (France)

^b CNRS   (France)

^c UNIVERSITÉ PARIS DESCARTES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

HETEROANNULATION; PALLADIUM-CATALYZED;

CATALYSIS;

CYCLIZATION;

2 (METHOXYMETHYL) 3 PHENYL 1H PYRROLO[3,2 C]PYRIDINE; 2 BUTYL 3 PHENYL 1H PYRROLO[3,2 C]PYRIDINE; 2 CYCLOHEXYL 3 PHENYL 1H PYRROLO[3,2 C]PYRIDINE; 2 CYCLOPROPYL 3 PHENYL 1H PYRROLO[3,2 C]PYRIDINE; 2 ISOBUTYL 3 PHENYL 1H PYRROLO[3,2 C]PYRIDINE; 2 ISOPROPYL 3 PHENYL 1H PYRROLO[3,2 C]PYRIDINE; 2 METHYL 3 PHENYL 1H PYRROLO[3,2 C]PYRIDINE; 2 PHENYL 3 (PYRIDIN 4 YL) 1H PYRROLO[3,2 C]PYRIDINE; 2,3 BIS(METHOXYMETHYL) 1H PYRROLO[3,2 C]PYRIDINE; 2,3 DIPROPYL 1H PYRROLO[3,2 C]PYRIDINE; 3 BUTYL 2 PHENYL 1H PYRROLO[3,2 C]PYRIDINE; 3 CYCLOHEXYL 2 PHENYL 1H PYRROLO[3,2 C]PYRIDINE; 3 ISOBUTYL 2 PHENYL 1H PYRROLO[3,2 C]PYRIDINE; 3 ISOPROPYL 2 PHENYL 1H PYRROLO[3,2 C]PYRIDINE; 3 PHENYL 2 (PYRIDIN 4 YL) 1H PYRROLO[3,2 C]PYRIDINE; 4 AMINO 2 BROMO 3 IODOPYRIDINE; 4 AMINO 2 BROMO 3,5 DIIODOPYRIDINE; 4 AMINO 2 BROMO 5 IODOPYRIDINE; 4 AMINO 2 CHLORO 3 IODOPYRIDINE; 4 AMINO 2 CHLORO 3,5 DIIODOPYRIDINE; 4 AMINO 2 CHLORO 5 IODOPYRIDINE; 4 AMINO 3 BROMO 5 IODOPYRIDINE; 4 AMINO 3 CHLORO 5 IODOPYRIDINE; 4 AMINO 3 IODOPYRIDINE; 4 AMINO 3,5 DIIODOPYRIDINE; 5 AZAINDOLE DERIVATIVE; INDOLE DERIVATIVE; PALLADIUM; PYRIDINE DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

ANNULATION REACTION; ARTICLE; CATALYSIS; CHEMICAL REACTION; CYCLIZATION; DOMINO SILA SONOGASHIRA REACTION; DRUG SYNTHESIS; HETEROANNULATION REACTION; SUBSTITUTION REACTION;

AZA COMPOUNDS; CATALYSIS; CYCLIZATION; INDOLES; MOLECULAR STRUCTURE; PALLADIUM;

EID: 84861803697     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo300481s     Document Type: Article

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