[1]
Cione E, Tucci P, Senatore V, et al. Synthesized esters of ferulic acid induce release of cytochrome c from rat testes mitochondria. Journal of bioenergetics and biomembranes, 40 (2008) 19-26.
DOI: 10.1007/s10863-007-9097-7
Google Scholar
[2]
Fang X, Kikuchi S, Shima M, et al. Suppressive effect of alkyl ferulate on the oxidation of microencapsulated linoleic acid. European Journal of Lipid Science and Technology, 108 (2006) 97-102.
DOI: 10.1002/ejlt.200500258
Google Scholar
[3]
Fang X, Shima M, Kadota M, et al. Suppressive effect of alkyl ferulate on the oxidation of linoleic acid. Bioscience, biotechnology, and biochemistry, 70(2006) 457-461.
DOI: 10.1271/bbb.70.457
Google Scholar
[4]
Chikuno T, Kato H, Kadota M. Skin-lightening cosmetics containing ferulic acid esters. JP 2005350425. (2005).
Google Scholar
[5]
Taniguchi H, Nomura E, Hosoda A, et al. Ferulic acid or derivative thereof as inhibitor and regulator of germination. JP 2003040709. (2003).
Google Scholar
[6]
Kikuzaki H, Hisamoto M, Hirose K, et al. Antioxidant Properties of Ferulic Acid and Its Related Compounds. Journal of Agricultural and Food Chemistry, 50 (2002) 2161-2168.
DOI: 10.1021/jf011348w
Google Scholar
[7]
Murakami A, Kadota M, Takahashi D, et al. Suppressive effects of novel ferulic acid derivatives on cellular responses induced by phorbol ester, and by combined lipopolysaccharide and interferon. Cancer Letters (Shannon, Ireland), 157 (2000) 77-85.
DOI: 10.1016/s0304-3835(00)00478-x
Google Scholar
[8]
Zhihua Song, Bo Gao, Xingguo Wang, et al. Enzymatic synthesis of feruloylated structolipids in two steps with a solvent-free system. China Oils and Fats, 34 (2009) 45-47. In Chinese.
Google Scholar
[9]
Qingfang Cheng, Qifa Wang, Xingyou Xu, et al. Synthesis of 3-Cinnamoylisoferulic Acid Phenyl Esters under Ultrasonic Irradiation. Chinese Journal of Pharmaceuticals, 41 (2010) 88-90. In Chinese.
Google Scholar
[10]
Jianhong Tang, Qingyou Zeng. One-pot Synthesis of 2-Ethylhexyl-3-(4-hydroxy-3-meth oxyphenyl) acrylate. Fine Chemicals, 27 (2010) 793-795. In Chinese.
Google Scholar
[11]
Yoshida Y, Kimura Y, Kadota M, et al. Continuous synthesis of alkyl ferulate by immobilized Candida antarctica lipase at high temperature. Biotechnology Letters, 28 (2006) 1471-1474.
DOI: 10.1007/s10529-006-9113-8
Google Scholar
[12]
Giuliani S, Piana C, Setti L, et al. Synthesis of pentylferulate by a feruloyl esterase from Aspergillus niger using water-in-oil microemulsions. Biotechnology Letters, 23 (2001) 325-330.
Google Scholar
[13]
Cassani J, Luna H, Navarro A, et al. Comparative esterification of phenylpropanoids versus hydrophenylpropanoids acids catalyzed by lipase in organic solvent media. Electronic Journal of Biotechnology, 10 (2007) 508-513.
DOI: 10.2225/vol10-issue4-fulltext-3
Google Scholar
[14]
Li N G, Shi Z H, Tang Yu P, et al. Highly efficient esterification of ferulic acid under microwave irradiation. Molecules, 14 (2009) 2118-2126.
DOI: 10.3390/molecules14062118
Google Scholar
[15]
Jiaying Xin, Yan Zhang, Guanli Zhao, et al. Application and Synthesis of Ferulic Acid and Its Derivatives. Chemical World, (2006) 305-307. In Chinese.
Google Scholar
[16]
Shengzhao Gong, Jia Li, Zhimian Yun, et al. Synthesis of amyl ferulate catalyzed by sodium hydrogen sulfate. Chemical Research and Application, 24 (2012) 94-96. In Chinese.
Google Scholar
[17]
Jayaprakasam B, Vanisree M, Zhang Y J, et al. Impact of Alkyl Esters of Caffeic and Ferulic Acids on Tumor Cell Proliferation, Cyclooxygenase Enzyme, and Lipid Peroxidation. Journal of Agricultural and Food Chemistry, 54 (2006) 5375-5381.
DOI: 10.1021/jf060899p
Google Scholar
[18]
Xiangwen Kong, Long Yu. Synthesis of n-butyl acetate catalyzed by solid superacid SO42-/Fe2O3. Experimental Technology and Management, 28(2011) 30-31, 40. In Chinese.
Google Scholar