Facile and efficient synthesis of 3,4,5-substituted furan-2(5H)-ones by using β-cyclodextrin as reusable catalyst

Tetrahedron

Volumn 65, Issue 27, 2009, Pages 5251-5256

  Narayana Murthy, S ^a   Madhav, B ^a   Vijay Kumar, A ^a   Rama Rao, K ^a   Nageswar, Y V D ^a  

^a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

Author keywords

[No Author keywords available]

Indexed keywords

2 (4 (BENZYLOXY)PHENYL) 2,5 DIHYDRO 5 OXO 4 PHENYLAMINO)FURAN 3 CARBOXYLIC ACID; 2 (4 CHLOROPHENYL) 2,5 DIHYDRO 5 OXO 4 (PHENYLAMINO)FURAN 3 CARBOXYLIC ACID; 2 (4 ETHOXYPHENYL) 2,5 DIHYDRO 5 OXO 4 (PHENYLAMINO)FURAN 3 CARBOXYLIC ACID; 2 (4 ETHYLPHENYL) 2,5 DIHYDRO 5 OXO 4 (PHENYLAMINO)FURAN 3 CARBOXYLIC ACID; 2,5 DIHYDRO 2 (4 METHOXYPHENYL) 5 OXO 4 (PHENYLAMINO)FURAN 3 CARBOXYLIC ACID; 2,5 DIHYDRO 2 (NAPHTHALEN 1 YL) 5 OXO 4 (PHENYLAMINO)FURAN 3 CARBOXYLIC ACID; 2,5 DIHYDRO 2 (NAPHTHALEN 3 YL) 5 OXO 4 (PHENYLAMINO)FURAN 3 CARBOXYLIC ACID; 2,5 DIHYDRO 5 OXO 2 PHENYL 4 (PHENYLAMINO)FURAN 3 CARBOXYLIC ACID; 2,5 DIHYDRO 5 OXO 4 (PHENYLAMINO) 2 PTOLYLFURAN 3 CARBOXYLIC ACID; 3,4,5 FURAN 2 (5H) ONE; 4 (3 CHLOROPHENYLAMINO) 2,5 DIHYDRO 5 OXO 2 PHENYLFURAN 3 CARBOXYLIC ACID; 4 (4 BUTYLPHENYLAMINO) 2,5 DIHYDRO 5 OXO 2 PHENYLFURAN 3 CARBOXYLIC ACID; 4 (4 CHLOROPHENYLAMINO) 2,5 DIHYDRO 5 OXO 2 PHENYLFURAN 3 CARBOXYLIC ACID; 4 (4 FLUOROPHENYLAMINO) 2,5 DIHYDRO 5 OXO 2 PHENYLFURAN 3 CARBOXYLIC ACID; 4 (4 IODOPHENYLAMINO) 2,5 DIHYDRO 5 OXO 2 PHENYLFURAN 3 CARBOXYLIC ACID; 4 (4 TOLYLAMINO) 2,5 DIHYDRO 5 OXO 2 PHENYLFURAN 3 CARBOXYLIC ACID; BETA CYCLODEXTRIN; CARBOXYLIC ACID DERIVATIVE; FURAN DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; BIOMIMETICS; CATALYSIS; CATALYST; CHEMICAL REACTION; CHEMICAL STRUCTURE; DRUG SYNTHESIS; HYDROPHOBICITY; PRIORITY JOURNAL; SUBSTITUTION REACTION;

EID: 66149133660     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2009.04.081     Document Type: Article

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