108401-87-2Relevant articles and documents
Synthesis, characterization and anticancer activity of a series of curcuminoids and their half-sandwich ruthenium(II) complexes
Li, Peiyuan,Su, Wei,Lei, Xiaolin,Xiao, Qi,Huang, Shan
, (2017/09/01)
A series of curcuminoids (L1–L7) and their corresponding (η6-p-cymene)RuII(Cur)Cl complexes (1–7) were synthesized and characterized using 1H NMR spectroscopy, elemental analysis and high-resolution e
Reductive ring opening of 3,5-bis(2-arylethenyl)isoxazoles with molybdenum hexacarbonyl: A novel route to symmetrical and unsymmetrical curcumin derivatives
Hahnvajanawong, Viwat,Thaima, Thanaphat,Tearavarich, Ruchanok,Theramongkol, Parinya
, p. 127 - 135 (2016/05/09)
Curcumin derivatives were successfully synthesized from 3,5-dimethylisoxazole by lateral metalation and condensation with various aromatic aldehydes sequentially at C5- and C3-methyl groups. After dehydration, further transformation of isoxazole ring to β-diketone moiety was accomplished by reductive ring opening using molybdenum hexacarbonyl [Mo(CO)6] and subsequent simple acidic hydrolysis.
Significant enhancement in radical-scavenging activity of curcuminoids conferred by acetoxy substituent at the central methylene carbon
Kim, Mi Kyoung,Jeong, Wooseong,Kang, Jihoon,Chong, Youhoon
experimental part, p. 3793 - 3800 (2011/08/06)
For a compound to be a radical-trapping antioxidant, the antioxidant-derived radical must be sufficiently inert to molecular oxygen as this would generate harmful chain-propagating peroxyl radicals. Curcumin has a unique structure with phenolic hydroxyl g
