Page 242 - 《精细化工》2023年第6期
P. 242
·1392· 精细化工 FINE CHEMICALS 第 40 卷
α-aminophosphonate moiety[J]. Science China Chemistry, 2011, 54: analytical reagnts for the determination of platinum metals (a
103-109. review)[J]. Oriental Journal of Chemistry, 1987, 3(2): 203-206.
[3] BIELENICA A, STEFANSKA J, STEPIEN K, et al. Synthesis, [13] ZUO T M (左天明), WANG C X (王彩霞), MA D L (马东兰).
cytotoxicity and antimicrobial activity of thioureaderivatives Application of thiourea reagents in inorganic analysis[J]. Journal of
incorporating 3-(trifluoromethyl) phenyl moiety[J]. European Journal Henan Normal University (Natural Science) (河南师范大学学报:自
of Medicinal Chemistry, 1998, 101: 111-125. 然科学版), 1991, 25 (1): 45-51.
[4] SAEED S, RASHID N, JONES P G, et al. Synthesis, spectroscopic [14] MAO X M (毛向敏), SONG R Y (宋瑞英). Mechanism of
characterization, crystal structure and antifungal activity of thiourea cross-linking neoprene rubber with ethylthiuria and zinc oxide
derivatives containing a thiazole moiety[J]. Central European Journal (Ⅰ)[J]. World Rubber Industry (世界橡胶工业), 2015, 42(7):
of Chemistry, 2010, 8: 550-558. 10-14.
[5] ABBAS S Y, EL-SHARIEF M A M S, BASYOUNI W M, et al. [15] SUN B T (孙宾涛). The study on synthesis and application of new
Thiourea derivatives incorporating a hippuric acid moiety: Synthesis thiourea antioxidant[D]. Xi'an: Shaanxi University of Science &
and evalution of antibacterial and antifungal activities[J]. European Technology (陕西科技大学), 2013.
Journal of Medicinal Chemistry, 2013, 64: 111-120. [16] VIANA G M, SOARES D C, SANTANA M V, et al. Antileishmanial
[6] YAO J W, CHEN J, HE Z P, et al. Design, synthesis and biological thioureas: Synthesis, biological activity and in silico evaluations of
activities of thiourea containing sorafenibanalogs as antitumor new promising derivatives[J]. Chemical and Pharmaceutical Bulletin,
agents[J]. Bioorganic & Medicinal Chemistry, 2012, 20: 2923-2929. 2017, 65: 911-919.
[7] LIU S Q, LOUIE M C, RAJAGOPALAN V, et al. Synthesis and [17] CHEN L (陈玲). Studies on the synthesis of thiourea/urea and
evaluation of the diarylthiourea analogs as novelanticancer agents[J]. benzoazole compounds by isothiocyanate in water[D]. Zhengzhou:
Bioorganic & Medicinal Chemistry Letters, 2015, 25: 1301-1305. Zhengzhou University (郑州大学), 2020.
[8] MAHAJAN A, YEH S, NELL M. Synthesis of new [18] TAVAKOL H, MAHMOUDI A, RANJBARI M A. Synthesis of di-
7-chloroquinolinyl thioureas and their biological investigation as and tri-substituted thiourea derivatives in water using choline
potential antimalarial and anticancer agents[J]. Bioorganic & chloride-urea catalyst[J]. Journal of Sulfur Chemistry, 2018, 40:
Medicinal Chemistry Letters, 2007, 17: 5683-5685. 113-123.
[9] WANG B, MA Y, XIONG L, et al. Synthesis and insecticidal activity [19] SONG Z Q (宋增强), ZHAN L L (詹玲玲), DING C C (丁超超),
of novel N-pyridyl pyrazole carbonylthioureas[J]. Chinese Journal of et al. The invention relates to a preparation method of asymmetric
Organic Chemistry, 2012, 30: 815-821. thiourea compounds: CN110330450A[P]. 2019-10-15.
[10] XUE S J, ZOU J S, YANG H J. Synthesis and herbicidal activities of [20] ZHANG H F (张慧芳). Improvement of synthesis process of N,
N'-(substituted pyrimidin-2-yl)-N-sub-stituted phenoxyacetyl thiourea N'-bis(2, 6-diisopropyl phenyl) thiourea[J]. Plastics Additive (塑料助
derivatives[J]. Chinese Chemical Letters, 2000, 11: 19-25. 剂), 2021, (5): 11-13.
[11] YONOVA P A, STOILKOVA G M J. Synthesis and biological [21] SHAHABI D, TAVAKOL H. Synthesis of 14H-dibenzo xanthene
activity of urea and thiourea derivatives from 2-amino heterocyclic derivatives using choline chloride/tin(Ⅱ) chloride deep eutectic
compounds[J]. Plant Growth Regulation, 2005, 23: 280-291. solvent and Fe 3O 4/ƛ-carrageenan/Zn(Ⅱ)[J]. Journal of the Iranian
[12] SINGH S, MATHUR S P, THAKUR R S, et al. Thiol reas as Chemical Society, 2016, 14(1): 1-8.
(上接第 1324 页) monitoring of free endogenous hydrogen sulfide[J]. Analytical
Chemistry, 2017, 89: 5382-5388.
[2] KAMOUN P, BELARDINELLI M C, CHABLI A, et al. Endogenous
hydrogen sulfide overproduction in Down syndrome[J]. American [12] YANG Z G (杨志广), ZHANG L Y (张璐瑶), CHEN Y H (陈亚红),
Journal of Medical Genetics, 2003, 116(3): 310-311. et al. Research progress of organic fluorescent small molecule probes
[3] ETO K, ASADA T, ARIMA K, et al. Brain hydrogen sulfide is for reactive sulfur species in mitochondria[J]. Fine Chemicals (精细
severely decreased in Alzheimer's disease[J]. Biochemical and 化工), 2018, 35(6): 901-909.
Biophysical Research Communications, 2002, 293: 1485-1488. [13] JOSE D A, SAKLA R, SHARMA N, et al. Sensing and bioimaging
[4] JIANG H L, WU H C, LI Z L, et al. Changes of the new gaseous of the gaseous signaling molecule hydrogen sulfide by near-infrared
transmitter H 2S in patients with coronary heart disease[J]. Journal of fluorescent probes[J]. ACS Sensors, 2020, 5(11): 3365-3391.
First Military Medical University, 2005, 25(8):951-954. [14] HE Y, CAI Y, HUANG W. Manganese dioxide nanosheets-induced
[5] KONOVALOV S K, ROMANOV A S. Spectrophotometric and oxidation of dopamine for colorimetric sensing of hydrogen
iodometric methods for the detection of hydrogen sulfide in the sulfide[J]. ChemistrySelect, 2017, 2(27): 8478-8482.
Black Sea: Comparison of the results of analysis[J]. Physical [15] CHA J H, KIM D H, CHOI S J, et al. Sub-parts-per-million hydrogen
Oceanography, 2000, 10(4): 365-377. sulfide colorimetric sensor: Lead acetate anchored nanofibers toward
[6] TANG D, SANTSCHI P H. Sensitive determination of dissolved halitosis diagnosis[J]. Analytical Chemistry, 2018, 90(15): 8769-8775.
sulfide in estuarine water by solid-phase extraction and high- [16] LEE J, LEE Y J, AHN Y J, et al. A simple and facile paper-based
performance liquid chromatography of methylene blue[J]. Journal of colorimetric assay for detection of free hydrogen sulfide in prostate
Chromatography A, 2000, 883(1/2): 305-309. cancer cells[J]. Sensors and Actuators B: Chemical, 2018, 256: 828-
[7] KOIKE S, KAWAMYRA K, KIMURA Y, et al. Analysis of 834.
endogenous H 2S and H 2S n in mouse brain by high-performance [17] ZHAO L Z. Paper-based analytical device for rapid naked-eye
liquid chromatography with fluorescence and tandem mass detection of sulfide in water samples[J]. Chemical Society of Pakistan,
spectrometric detection[J]. Free Radical Biology & Medicine, 2017, 2020, 42(5): 696-703.
113:355-362. [18] CHEN Z, CHEN C, HUANG H, et al. Target-induced horseradish
[8] SHAH S S, AZIZ M A, OYAMAM, et al. Controlled-potential-based peroxidase deactivation for multicolor colorimetric assay of hydrogen
electrochemical sulfide sensors: A review[J]. The Chemical Record, sulfide in rat brain microdialysis[J]. Analytical Chemistry, 2018,
2021, 21(1): 204-238. 90(10): 6222-6228.
[9] HAll J R, SCHOENFISCH M H. Direct electrochemical sensing of [19] HOSOKI R, MATSUKI N, KIMURA H. The possible role of
hydrogen sulfide without sulfur poisoning[J]. Analytical Chemistry, hydrogen sulfide as an endogenous smooth muscle relaxant in
2018, 90(8): 5194-5200. synergy with nitric oxide[J]. Biochemical and Biophysical Research
[10] YE C, XU F, WU Z, et al. Ultrasensitive photoelectrochemical Communications, 1997, 237(3): 527-531.
platform with micro-emulsion-based p-type hollow silver iodide [20] BERNINI F, CASTELLINI E, MALFERRARI D, et al. Effective
enabled by low solubility product (Ksp) for H 2S sensing[J]. and selective trapping of volatile organic sulfur derivatives by
Nanotechnology, 2021, 32(41): 415501. montmorillonite intercalated with a μ-oxo Fe(Ⅲ)-phenanthroline
[11] WANG S J, LIU X M, ZHANG M N. Reduction of complex[J]. ACS Applied Materials & Interfaces, 2017, 9(1): 1045-
)
ammineruthenium(Ⅲ by sulfide enables in vivo electrochemical 1056.