Page 234 - 《精细化工》2021年第8期

·1728· 精细化工 FINE CHEMICALS 第 38 卷

delaminated layered europium hydroxide (LEuH) composites with [24] BODAGHIFARD M A, SOLIMANNEJAD M, ASADBEGI S. Mild
sensitizer anions of coumarin-3-carboxylic acid[J]. Dalton and green synthesis of tetrahydrobenzopyran, pyranopyrimidinone
Transactions, 2017, 46(37): 12724-12731. and polyhydroquinoline derivatives and DFT study on product
[11] SURESH D K, SANDHU J S. Synthesis of 5-arylidene-2, 2-dimethy-l, structures[J]. Research on Chemical Intermediates, 2016, 42(2):
3-dioxane-4, 6-diones and coumarin-3-carboxylic acids via reaction 1165-1179.
of nitrones and meldrum′s acid[J]. Indian Journal of Chemistry [25] GAWANDE M B, BONIFCIO V D B, LUQUE R, et al. Benign by
Section B, 2013, 52B(8): 1157-1160. design: Catalyst-free in-water, on-water green chemical methodologies
[12] MAHADEVAN K M, HARISHKUMAR H N, MASAGALLI J N, et al. in organic synthesis[J]. Chemical Society Reviews, 2013, 42(12):
Synthesis and liquid crystal property of new fluoro coumarin 5522-5551.
carboxylates[J]. European Journal of Medicinal Chemistry, 2013, [26] XIAO J, WEN H, WANG L, et al. Catalyst-free dehydrative
570(1): 20-35. SN1-type reaction of indolyl alcohols with diverse nucleophiles ″
[13] ELIAS R, BENHAMOU R I, JABER Q Z, et al. Antifungal activity, on water″[J]. Green Chemistry, 2016, 18(4): 1032-1037.
mode of action variability, and subcellular distribution of coumarin-based [27] XI G L (席高磊), WANG Z W (王正伟), MA F (马飞), et al.
antifungal azoles[J]. European Journal of Medicinal Chemistry, 2019, Synthesis and antioxidant properties of ferrocenyl imid-azo[1,
179: 779-790. 2-a]pyridine compounds[J]. Fine Chemicals (精细化工), 2020, 37(2):
[14] YUAN S Q (袁书清), LI L (李丽), ZENG H Y (曾鸿耀), et al. 332-338.
“One-pot” synthesis of coumarin-3-carboxylic acids catalyzed by [28] ZHANG X P (张晓平), CHEN Z F (陈芝飞), HAN L (韩路), et al.
l-proline[J]. Chemical Research and Application (化学研究与应用), Synthesis and antioxidant properties of pyrazine-oxazole bi-heteroaryl
2017, 29(7): 1012-1018. compounds[J]. Fine Chemicals (精细化工), 2020, 37(7): 1461-1468.
[15] LIU X J (刘秀娟), LI L B (厉连斌), WANG G Y (王歌云). Studies [29] XI G L (席高磊), XU K J (许克静), WANG H W (王宏伟), et al.
on synthesis of coumarin-3-carboxylic acid and its ester[J]. Chemical Antioxidant properties of 4-methyl-7-hydroxycoumarin and derivative[J].
Reagents (化学试剂), 2007, 29(1): 43-45. Fine Chemicals (精细化工), 2019, 36(6): 1159-1165.
[16] YANG W S (杨文生). Study on preparation and spectroscopic [30] SUGDEN K D, WETTERHAHN K E. Direct and hydrogen
properties of coumarin-3-carboxylic acid[J]. Chemical Engineer (化 peroxide-induced chromium( Ⅴ ) oxidation of deoxyribose in
学工程师), 2016, 30(11): 82-85. single-stranded and double-stranded calf thymus DNA[J]. Chemical
[17] LUO Z C (罗志臣), DING Y S (丁元生). Sodium ethoxde catalyed Research in Toxicology, 1997, 10(12): 1397-1406.
synthesis of coumarin-3-carboxylic acids[J]. Speciality Petrochemicals [31] JANICEK M F, HASELTINE W A, HENNER W D. Malondial-
(精细石油化工), 2009, 26(4): 5-7. dehyde precursors in gamma-irradiated DNA, deoxynucleotides and
[18] RUAN H L (阮鸿力), ZHANG J Y (张婧园), SUN S(孙赛), et al. deoxynucleosides [J]. Nucleic Acids Research, 1985, 13(24): 9011-9029.
N-Bromosuccinimide mediated the reaction of 2-hydroxyaryl [32] XI G L, LIU Z Q. Coumarin sharing the benzene ring with quinoline
aldehydes with meldrum’s acid for synthesis of coumarin-3-carboxylic for quenching radicals and inhibiting DNA oxidation[J]. European
acids[J]. Chinese Journal of Organic Chemistry (有机化学), 2017, Journal of Medicinal Chemistry, 2015, 95: 416-423.
37(8): 2139-2144. [33] XI G L, LIU Z Q. Introducing ferrocene into imidazo[1,2-a]pyridine
[19] ZENG H Y (曾鸿耀), LI L (李丽), QIN H (覃夯). Green synthesis of by groebke three-component-reaction for scavenging radicals and
coumarin-3-carboxylic acid catalyzed by sulfamic acid in water[J]. inhibiting DNA oxidation[J]. Tetrahedron, 2015, 71(52): 9602-9610.
Journal of Leshan Normal University (乐山师范学院学报), 2019, [34] XI G L, LIU Z Q. Coumarin moiety can enhance abilities of
34(8): 17-24. chalcones to inhibit DNA oxidation and to scavenge radicals[J].
[20] WANG X (王潇), HAN X E (韩相恩). Studies on catalysis of Tetrahedron, 2014, 70(44): 8397-8404.
coumarin-3-carboxylic acid in ionic liquid[J]. Science & Technology [35] XI G L, LIU Z Q. Solvent-free povarov reaction for synthesizing
in Chemical Industry (化工科技), 2011, 19(6): 34-36. ferrocenyl quinolines: Antioxidant abilities deriving from ferrocene
[21] XIAO D (肖迪), ZHENG W (郑旺), WEI X Y (魏晓玉), et al. moiety[J]. European Journal of Medicinal Chemistry, 2014, 86(9):
Choline chloride promoted synthesis of coumarin-3-carboxylic 759-768.
acids[J]. Chinese Journal of Applied Chemistry (应用化学), 2017, [36] XI G L, LIU Z Q. Coumestan inhibits radical-induced oxidation of
34(11): 1295-1300. DNA: Is hydroxyl a necessary functional group[J]. Journal of
[22] FIORITO S, GENOVESE S, TADDEO V A, et al. Microwave-assisted Agricultural and Food Chemistry, 2014, 62(24): 5636-5642.
synthesis of coumarin-3-carboxylic acids under ytterbium triflate [37] STOJANOVIC S, BREDA O. Elementary reactions of the antioxidant
catalysis[J]. Tetrahedron Letters, 2015, 56, 2434-2436. action of trans-stilbene derivatives: Resveratrol, pinosylvin and
[23] GU Y L. Multicomponent reactions in unconventional solvents: State 4-hydroxystilbene[J]. Physical Chemistry Chemical Physics, 2002,
of the art[J]. Green Chemistry, 2012, 14(8): 2091-2128. 4(5): 757-764.