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Synthesis of some curcumin analogues under ultrasound irradiation
被引:1
|作者:
Lei Yingjie
[1
]
Ye, Bi
[1
]
Jie, Ouyang
[1
]
机构:
[1] Tianjin Univ Technol, Sch Chem & Chem Engn, Tianjin, Peoples R China
来源:
关键词:
Curcumin analogues;
Synthesis;
Ultrasound irradiation;
D O I:
10.4028/www.scientific.net/AMR.332-334.1623
中图分类号:
TB3 [工程材料学];
TS1 [纺织工业、染整工业];
学科分类号:
0805 ;
080502 ;
0821 ;
摘要:
A convenient method to synthesize curcumin and its five analogues, which were named as 1,7-diphenyl-1,6-heptadiene-3,5-dione,1,7-Bis-(4-hydroxy-phenyl)-1,6-heptadiene-3,5-dione,1,7-Bis-(4-methoxy-phenyl)-1,6-heptadiene-3,5-dione,1,7-Bis-(2-hydroxy-3-methoxy-phenyl)-1,6-heptadi ene-3,5-dione and 1,7-Bis-(2,3-dimethoxy-phenyl)-1,6-heptadiene-3,5-dione respectively, via the Claisen condensation of aromatic aldehyde and 2,4-pentanedione in the presence of trimethyl borate and monoethanolamine under ultrasound irradition was reported. The corresponding physical properties were characterized by IR, 1HNMR spectra and elemental analysis studies.
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页码:1623 / 1626
页数:4
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