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Volumn 67, Issue 16, 2011, Pages 2870-2877

Synthesis of C3-nitroalkylated-4-hydroxycoumarin and hydroxyiminodihydrofuroquinolinone derivatives via the Michael addition of cyclic 1,3-dicarbonyl compounds to β-nitrostyrenes

Author keywords

[No Author keywords available]

Indexed keywords

2 (HYDROXYIMINO) 3 (2 METHOXYPHENYL) 5 METHYL 2,3 DIHYDROFURO[3,2 C]QUINOLIN 4(5H) ONE; 2 (HYDROXYIMINO) 3 (4 METHOXYPHENYL) 5 METHYL 2,3 DIHYDROFURO[3,2 C]QUINOLIN 4(5H) ONE; 2 (HYDROXYIMINO) 5 METHYL 3 (NAPHTHALEN 2 YL) 2,3 DIHYDROFURO[3,2 C]QUINOLIN 4(5H) ONE; 2 (HYDROXYIMINO) 5 METHYL 3 4 TOLYL 2,3 DIHYDROFURO[3,2 C]QUINOLIN 4(5H) ONE; 2 (HYDROXYIMINO) 5 METHYL 3 PHENYL 2,3 DIHYDROFURO[3,2 C]QUINOLIN 4(5H) ONE; 3 (1 (2 FLUOROPHENYL) 2 NITROETHYL) 4 HYDROXY 2H CHROMEN 2 ONE; 3 (1 (4 CHLOROPHENYL) 2 NITROETHYL) 4 HYDROXY 2H CHROMEN 2 ONE; 3 (1 (4 FLUOROPHENYL) 2 NITROETHYL) 4 HYDROXY 2H CHROMENE 2 ONE; 3 (1 (FURAN 2 YL) 2 NITROETHYL) 4 HYDROXY 2H CHROMEN 2 ONE; 3 (2,6 DICHLOROPHENYL) 2 (HYDROXYIMINO) 5 METHYL 2,3 DIHYDROFURO[3,2 C]QUINOLIN 4(5H) ONE; 3 (3,4 DIMETHOXYPHENYL) 2 (HYDROXYIMINO) 5 METHYL 2,3 DIHYDROFURO[3,2 C]QUINOLIN 4(5H) ONE; 4 HYDROXY 1 METHYLQUINOLIN 2(1H) ONE; 4 HYDROXY 3 (1 (2 METHOXYPHENYL) 2 NITROETHYL) 2H CHROMEN 2 ONE; 4 HYDROXY 3 (1 (3 METHOXYPHENYL) 2 NITROETHYL) 2H CHROMEN 2 ONE; 4 HYDROXY 3 (1 (4 METHOXYPHENYL) 2 NITROETHYL) 2H CHROMEN 2 ONE; 4 HYDROXY 3 (1 (NAPHTHALEN 2 YL) 2 NITROETHYL) 2H CHROMEN 2 ONE; 4 HYDROXY 3 (2 NITRO 1 (2 (TRIFLUOROMETHYL)PHENYL)ETHYL) 2H CHROMEN 2 ONE; 4 HYDROXY 3 (2 NITRO 1 (2 NITROPHENYL)ETHYL) 2H CHROMEN 2 ONE; 4 HYDROXY 3 (2 NITRO 1 (4 NITROPHENYL)ETHYL) 2H CHROMEN 2 ONE; 4 HYDROXY 3 (2 NITRO 1 4 TOLYLETHYL) 2H CHROMEN 2 ONE; 4 HYDROXY 3 (2 NITRO 1 PHENYLETHYL) 2H CHROMEN 2 ONE; 4 HYDROXYCOUMARIN DERIVATIVE; ALKENE DERIVATIVE; HYDROGEN; HYDROXYIMINODIHYDROFUROQUINOLINONE DERIVATIVE; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 79953170500     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2011.02.062     Document Type: Article
Times cited : (27)

References (85)
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    • For biological activities of coumarin
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    • For the syntheis of Angular furoquinolinone
    • For the syntheis of Angular furoquinolinone:
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    • For the recent publications on C3-alkylation of 4-hydroxycoumarin
    • For the recent publications on C3-alkylation of 4-hydroxycoumarin:
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    • For the syntheis of furoquinolinone
    • For the syntheis of furoquinolinone:
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    • CCDC number of the 12a and 15a are 793324 and 793322 respectively. These data can be obtained free of charge from Cambridge Crystallographic Data Center via
    • CCDC number of the 12a and 15a are 793324 and 793322 respectively. These data can be obtained free of charge from Cambridge Crystallographic Data Center via www.ccdc.cam.ac.uk/datarequest/cif.
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    • We are thankful the reviewer for his valuable suggestion regarding the mechanism
    • We are thankful the reviewer for his valuable suggestion regarding the mechanism.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.