Montmorillonite K-1O clay catalyzed solvent-free synthesis of bis-indolylindane1,3-dione, 2-(1′,3′-dihydro-1 H-[2,3′] biindolyl-2-ylidene)-indan-1,3-dione and bisindolylindeno[ 1,2-b]quinoxaline under microwave irradiation

Tetrahedron

Volumn 66, Issue 27-28, 2010, Pages 5196-5203

  Naskar, Subhendu ^a   Paira, Priyankar ^a   Paira, Rupankar ^a   Mondal, Shyamal ^a   Maity, Arindam ^a   Hazra, Abhijit ^a   Sahu, Krishnendu B ^a   Saha, Pritam ^a   Banerjee, Sukdeb ^a   Luger, Peter ^b   Webe, Manuela ^b   Mondal, Nirup B ^a  

^a INDIAN INSTITUTE OF CHEMICAL BIOLOGY   (India)

^b FREIE UNIVERSITÄT BERLIN   (Germany)

Author keywords

Indole; Microwave; Montmorillonite K 10; Ninhydrin; Solvent free condition

Indexed keywords

11,11 BIS (1 METHYL 1H INDOL 3 YL) 11H INDENO[1,2 B]QUINOXALINE; 11,11 BIS (1H INDOL 3 YL) 11H INDENO[1,2 B]QUINOXALINE; 11,11 BIS (1H INDOL 3 YL) 7,8 DIMETHYL 11H INDENO[1,2 B]QUINOXALINE; 11,11 BIS (5 BROMO 1H INDOL 3 YL) 11H INDENO[1,2 B]QUINOXALINE; 11,11 BIS (5 METHOXY 1H INDOL 3 YL) 11H INDENO[1,2 B]QUINOXALINE; 11,11 BIS (5 METHOXY 1H INDOL 3 YL) 7,8 DIMETHYL 11H INDENO[1,2 B]QUINOXALINE; 2 (3,3' DIMETHYL 1',3' DIHYDRO 1H [2,3']BIINDOLYL 2' YLIDENE)INDAN 1,3 DIONE; 2,2 BIS (1 METHYL 1H INDOL 3 YL)INDAN 1,3 DIONE; 2,2 BIS (1H INDOL 3 YL)INDAN 1,3 DIONE; 2,2 BIS (2 METHYL 1H INDOL 3 YL)INDAN 1,3 DIONE; 2,2 BIS (5 BROMO1H INDOL 3 YL)INDAN 1,3 DIONE; 2,2 BIS (5 METHOXY 1H INDOL 3 YL)INDAN 1,3 DIONE; 7,8 DICHLORO 11,11 BIS (1 METHYL 1H INDOL 3 YL) 11H INDENO[1,2 B]QUINOXALINE; 7,8 DIMETHYL 11,11 BIS (1 METHYL 1H INDOL 3 YL) 11H INDENO[1,2 B]QUINOXALINE; 7,8 DIMETHYL 11,11 BIS (2 METHYL 1H INDOL 3 YL) 11H INDENO[1,2 B]QUINOXALINE; MONTMORILLONITE; NINHYDRIN; QUINOXALINE DERIVATIVE; UNCLASSIFIED DRUG; [3' CARBOXYMETHYL 2' (1,3 DIOXO INDAN 2 YLIDENE) 2'3' DIHYDRO 1H,1'H [2,3']BIINDOLYL 3 YL]ACETIC ACID;

ARTICLE; CATALYSIS; CATALYST; CLAY; DRUG STRUCTURE; DRUG SYNTHESIS; MICROWAVE IRRADIATION; PRIORITY JOURNAL; SUBSTITUTION REACTION;

EID: 77954349168     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2010.04.084     Document Type: Article

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