A convenient iodination of indoles and derivatives

Tetrahedron

Volumn 68, Issue 31, 2012, Pages 6269-6275

  Hamri, Salha ^a   Rodríguez, Jose ^a   Basset, Joan ^a   Guillaumet, Gérald ^b   Dolors Pujol, M ^a  

^a UNIVERSITY OF BARCELONA   (Spain)

^b UNIVERSITÉ D'ORLÉANS   (France)

Author keywords

Electrophilic substitution; Iodine reagents and iodination; Iodoazaindoles; Iodoindoles

Indexed keywords

1 ETHYL 5 IODO 2 METHYL 3 (METHYLSULFONYL) 1H PYRROLE; 2 (2 IODO 1H INDOL 3 YL)ACETONITRILE; 2 IODO 1 [1 (4 METHOXYPHENYLSULFONYL) 1H INDOL 3 YL)ETHANONE; 2 IODO 1H PYRROLO[2,3 B]PYRIDINE; 2 IODO 2 (2 IODO 1H INDOL 3 YL)ACETONITRILE; 2,2 DIIODO 1 [2 IODO 1 (4 METHOXYPHENYLSULFONYL) 1H INDOL 3 YL]ETHANONE; 2,3 DIIODO 1 (PHENYLSULFONYL) 1H PYRROLO[2,3 B]PYRIDINE; 3 (2 BROMOETHYL) 2 IODO 1H INDOLE; 3 IODO 1H PYRROLO[2,3 B]PYRIDINE; 4 IODO 1 METHYL 1H PYRROLE 2 CARBALDEHYDE; 5 BROMO 2,3 DIIODO 1H INDOLE; AZAINDOLE DERIVATIVE; INDOLE; INDOLE DERIVATIVE; IODINE; N [2 (2 IODO 1H INDOL 3 YL)ETHYL]ACETAMIDE; N [2 (2 IODO 5 METHOXY 1H INDOL 3 YL)ETHYL]ACETAMIDE; PYRROLE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL REACTION; CHEMICAL STRUCTURE; ELECTROPHILICITY; IODINATION; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; STOICHIOMETRY; SUBSTITUTION REACTION; SYNTHESIS;

EID: 84862703788     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2012.05.053     Document Type: Article

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