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第 1 期 李 媛，等: 研磨强化无溶剂法合成蔗糖脂肪酸酯 ·123·

参考文献： European Food Research and Technology, 2013, 237(2): 237-244.
[11] Li Zuyi (李祖义), Shi Yiping (施邑屏), Yuan Changgui (袁长贵).
[1] Robert J W. Emulsifiers in food technology[M]. Blackwell The synthesis of sucrose esters by homogeneous non-solvent
Publishing Ltd，2004: 131-158. method[J]. Shanghai Chemical Industry (上海化工), 1999, 24(19):
[2] Douglas K A, Bernard Y T. Carbohydrate-alkyl ester derivatives as 16-17.
biosurfactants[J]. Journal of Surfactants and Detergents, 1999, 2(3): [12] Peng Yangxi (彭秧锡), Chen Qiyuan (陈启元), Liu Shijun (刘士军),
383-390. et al. Research status and prospect of mechanochemistry[J].
[3] Ran Y, Douglas G H, Rachel B. Effects of particle size of sucrose Materials Science＆Technology (材料科学与工艺), 2009, 17(1):
suspensions and pre-incubation of enzymes on lipase-catalyzed 113-117.
synthesis of sucrose oleic acid esters[J]. Journal of the American Oil [13] Mugunthan G, Ravindranathan Kartha K P. Application of ball milling
Chemists’ Society, 2014, 91(11): 1891-1901. technology to carbohydrate reactions-II:Solvent-free mechanochemical
[4] Lin X S, Zou Y, Zhao K H, et al. Tetraalkylammonium ionic liquids synthesis of glycosylazides[J]. Journal of Carbohydrate Chemistry,
as dual solvents-catalysts for direct synthesis of sugar fatty acid 2008, 27(5): 294-299.
esters[J]. Journal of Surfactants and Detergents, 2016, 19(3): [14] Li Kai (李凯), Meng Lidan (蒙丽丹), Su Jiating (苏佳廷), et al.
511-517. Synthesis of sucrose laurate via transesterification underdual-
[5] Tomone S, Yuto K, Naomi S K. Process design for green and frequency ultrasonic irradiation[J]. Applied Chemical Industry (应用
selective production of bio-based surfactant with heterogeneous resin 化工), 2016, 45(7): 1224-1227.
catalyst[J]. Chemical Engineering Journal, 2018, 334: 2231-2237. [15] The Joint FAO/WHO Expert Committee on Food Additives (JECFA):
[6] Zhang Yadong (章亚东), Gao Xiaolei (高晓蕾), Jiang Denggao (蒋 73rd JECFA (2010) FAO JECFA Monographs. Sucrose esters of fatty
登高), et al. Synthesis of sucrose ester with no-solvent method[J]. acids[S]. Food and Agriculture Organization of the United Nations,
Journal of Chemical Engineering of Chinese Universities (高校化学 2010: 10.
工程学报), 2002, 5 (16): 519-523. [16] People's Republic of China National Health and Family Planning
[7] Fitremann J, Queneau Y, Maitre J P, et al. Co-melting of solid Commission (中华人民共和国国家卫生和计划生育委员会). Food
sucrose and multivalent cation soaps for solvent-free synthesis of additivessucrose fatty acid ester (食品添加剂蔗糖脂肪酸酯):
sucrose esters[J]. Tetrahedron Letters, 2007, 48(23): 4111-4114. GB1886.27—2015[S]. Beijing: China Standard Publishing House,
[8] Tülay P, Robert J L. Syntheses and applications of sucrose-based 2015: 9-22.
esters[J]. Journal of Surfactants and Detergents, 2001, 4(4): 415-421. [17] State General Administration of the People's Republic of China for
[9] Wang Q H, Zhang S F, Yang J Z. Regioselective formation of Quality Supervision and Inspection andQuarantine (中华人民共和国
6-O-acylsucroses and 6, 3-di-O-acylsucroses via the 国家质量监督检验检疫总局)，China National Standardization
stannyleneacetalmethod[J]. Carbohydrate Research, 2007, 342(17): Administration (中国国家标准化管理委员会). Determination of
2657-2663. ignition residue for organic chemical products (有机化工产品灼烧
[10] Lu Y Y, Yan R, Ma X, et al. Synthesis and characterization of 残渣的测定 ): GB/T 7531 — 2008[S]. Beijing: China Standard
raffinose fatty acid monoesters under ultrasonic irradiation[J]. Publishing House, 2008: 6-4.

2+
（上接第 117 页） 2-amine-based high selective fluorescent sensor for Zn , from
nopinone[J]. Tetrahedron, 2016, 72(30): 4503-4509.
[17] Yang J, Xu H, Xu X, et al. Synthesis, optical properties, and cellular
[9] Wang S, Wu B, Xue J, et al. Nizatidine, a small molecular
compound, enhances killed H 5N 1 vaccine cell-mediated responses imaging of novel quinazolin-2-amine nopinone derivatives[J]. Dyes
& Pigments, 2016, 128: 75-83.
and protects mice from lethal viral challenge[J]. Human Vaccines,
[18] Rui Jian (芮坚), Zhang Qi (张齐), Wang Xin (王欣), et al. Synthesis
2014, 10(2): 461-468. and biological activity of novel pinanyl pyrazole acetamide
[10] Gao Yanqing (高艳清). Synthesis and antibacterial and antitumor derivatives[J]. Organic Chemistry (有机化学), 2017, 37(1): 218-225.
activity of β-Pinene derivatives[D]. Beijing:Chinese Academy of [19] Sun Nan (孙楠), Wang Xin (王欣), Ding Zhibin (丁志彬), et al.
Forestry (中国林业科学研究院), 2013.
Synthesis and biological activity of novel pinanyl thiazole derivatives
[11] Zhao Zhendong (赵振东), Liu Xianzhang (刘先章). Fine chemical
[J]. Organic Chemistry (有机化学), 2016, 36(10): 2489-2495.
utilization of turpentine oil[J]. Biomass Chemical Engineering (生物 [20] Wang Y, Gu W, Shan Y, et al. Design, synthesis and anticancer
质化学工程), 2001, 35: 38-43. activity of novel nopinone-based thiosemicarbazone derivatives[J].
[12] Paruch E, Ciunik Z, Nawrot J, et al. Synthesis of terpenoid lactones- Bioorganic & Medicinal Chemistry Letters, 2017, 27(11): 2360-
active insect antifeedants[J]. Journal of Agricultural & Food Chemistry, 2363.
2000, 48(10): 4973-4977. [21] Ni G, Tang Y, Li M, et al. Synthesis of scutellarein derivatives with a
[13] Samarasekera R, Weerasinghe I S, Hemalal K P. Insecticidal activity long aliphatic chain and their biological evaluation against human
of menthol derivatives against mosquitoes[J]. Pest Management cancer cells[J]. Molecules, 2018, 23(2): 310-316.
Science, 2010, 64(3): 290-295. [22] Liu Bing (刘兵), Ao Wangwei (敖汪伟), Yang Yang (杨杨), et al.
[14] Zahran H, Abdelgaleil S. Insecticidal and developmental inhibitory Synthesis of (+)-nopinone from (-)-β-pinene by selective
properties of monoterpenes on Culex pipiens L. (Diptera: Culicidae) oxidation[J]. Journal of Nanjing Forestry University (南京林业大学
[J]. Journal of Asia-Pacific Entomology, 2011, 14(1): 46-51. 学报), 2010, 34(2): 89-94.
[15] Yang J, Xu X, Rui J, et al. Synthesis, optical properties and [23] Huang X, Huang R, Gou S, et al. Combretastatin A-4 analogue: A
application of a set of novel pyrazole nopinone derivatives[J]. dual-targeting and tubulin inhibitor containing antitumor Pt(Ⅳ)
Spectrochim Acta A Mol Biomol Spectrosc, 2017, 183: 60-67. moiety with a unique mode of action[J]. Bioconjug Chem, 2016,
[16] Yang J, Fang H, Fang X, et al. A novel tetrahydroquinazolin- 27(9): 2132-2148.