Platinum-catalyzed, one-pot tandem synthesis of indoles and isoquinolines via sequential rearrangement of amides and aminocyclization

Journal of Organic Chemistry

Volumn 75, Issue 22, 2010, Pages 7615-7625

  Okamoto, Noriko ^a,b   Takeda, Kei ^b   Yanada, Reiko ^a  

^a HIROSHIMA INTERNATIONAL UNIVERSITY   (Japan)

^b HIROSHIMA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ALKYNYLS; AMINOCYCLIZATION; EFFICIENT SYNTHESIS; ELECTROPHILIC CARBON; ISOCYANATE INTERMEDIATES; ISOQUINOLINES; LEWIS ACID CATALYSTS; MACROCYCLICS; NUCLEOPHILIC ADDITIONS; ONE POT; PHOSPHORANES; WITTIG REAGENTS;

ACIDS; ADDITION REACTIONS; AMIDES; AMINES; CHLORINE COMPOUNDS; METABOLISM; MICROWAVE IRRADIATION; PLATINUM; SYNTHESIS (CHEMICAL); UREA;

REACTION RATES;

1,2 DIHYDROISIOQUINOLINE CARBAMATE DERIVATIVE; 2 ALKYLNYLBENZAMIDE DERIVATIVE; 2 ALKYLNYLBENZYLAMIDE DERIVATIVE; ALCOHOL DERIVATIVE; AMIDE; AMINE; BENZAMIDE DERIVATIVE; BENZYL 2 BUTYL INDOLE 1 CARBOXYLATE; BENZYL 3 PHENYLISOQUINOLINE 2(1H) CARBOXYLATE; CARBAMIC ACID DERIVATIVE; ETHYL 2 (3 TOSYLOXY) PROPYL INDOLE 1 CARBOXYLATE; ETHYL 2 BUTYL 3 (3 METHOXY 3 OXOPROP 1 ENYL) INDOLE 1 CARBOXYLATE; ETHYL 2 BUTYL 6 FLUORO INDOLE 1 CARBOXYLATE; ETHYL 2 BUTYL 6 NITRO INDOLE 1 CARBOXYLATE; ETHYL 3 4TOLYLISOQUINOLINE 2(1H) CARBOXYLATE; ETHYL 3 PHENYLISOQUINOLINE 2(1H) CARBOXYLATE; INDOLE CARBAMATE DERIVATIVE; INDOLE DERIVATIVE; INDOLE PHOSPHORANE DERIVATIVE; INDOLE UREA DERIVATIVE; ISOCYANATE; ISOQUINOLINE DERIVATIVE; LEWIS ACID; MACROCYCLIC COMPOUND; METHYL 3 PHENYLISOQUINOLINE 2(1H) CARBOXYLATE; PHOSPHORANE DERIVATIVE; PLATINUM; PLATINUM COMPLEX; UNCLASSIFIED DRUG; UNINDEXED DRUG; UREA DERIVATIVE;

AMINOCYCLIZATION; ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CYCLIZATION; ELECTROPHILICITY; MICROWAVE IRRADIATION; NUCLEOPHILICITY; ONE POT SYNTHESIS; WITTIG REACTION;

AMIDES; CARBAMATES; CATALYSIS; CYCLIZATION; INDICATORS AND REAGENTS; INDOLES; ISOQUINOLINES; LEWIS ACIDS; MICROWAVES; MOLECULAR STRUCTURE; PLATINUM;

EID: 78449245050     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo101347f     Document Type: Article

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