Facile synthesis of chiral 2-amino-4-(indol-3-yl)-4H-chromene derivatives using thiourea as the catalyst

Tetrahedron Asymmetry

Volumn 24, Issue 20, 2013, Pages 1312-1317

  Gao, Yu ^a   Du, Da Ming ^a  

^a BEIJING INSTITUTE OF TECHNOLOGY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

2 AMINO 4 (1H INDOL 3 YL) 4H CHROMENE 3 CARBONITRILE; 2 AMINO 4 (1H INDOL 3 YL) 6 BROMO 4H CHROMENE 3 CARBONITRILE; 2 AMINO 4 (1H INDOL 3 YL) 6 CHLORO 4H CHROMENE 3 CARBONITRILE; 2 AMINO 4 (1H INDOL 3 YL) 6 METHOXY 4H CHROMENE 3 CARBONITRILE; 2 AMINO 4 (1H INDOL 3 YL) 6,8 DICHLORO 4H CHROMENE 3 CARBONITRILE; 2 AMINO 4 (1H INDOL 3 YL) 8 ETHOXY 4H CHROMENE 3 CARBONITRILE; 2 AMINO 4 (1H INDOL 3 YL) 8 METHOXY 4H CHROMENE 3 CARBONITRILE; 2 AMINO 4 (5 CHLORO 1H INDOL 3 YL) 4H CHROMENE 3 CARBONITRILE; 2 AMINO 4 (5 METHYL 1H INDOL 3 YL) 4H CHROMENE 3 CARBONITRILE; 2 AMINO 4 (5 METHYL 1H INDOL 3 YL) 6 BROMO 4H CHROMENE 3 CARBONITRILE; 2 AMINO 4 (5 METHYL 1H INDOL 3 YL) 6 METHOXY 4H CHROMENE 3 CARBONITRILE; 2 AMINO 4 (5 METHYL 1H INDOL 3 YL) 8 METHOXY 4H CHROMENE 3 CARBONITRILE; 2 AMINO 4 (INDOL 3 YL) 4H CHROMENE DERIVATIVE; CHROMENE DERIVATIVE; INDOLE DERIVATIVE; THIOUREA; UNCLASSIFIED DRUG;

ARTICLE; CATALYST; DRUG SYNTHESIS; ENANTIOSELECTIVITY; KNOEVENAGEL CONDENSATION; PINNER REACTION; PRIORITY JOURNAL;

EID: 84886952060     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2013.08.018     Document Type: Article

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