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Novozyme 435选择性酸解(R,S)-3-n-丁基苯酞 被引量:1

Enantiomeric Selective Acidolysis of(R,S)-3-n-butylphthalide Catalyzed by Novozyme 435
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摘要 Novozyme 435可以提高对映体选择性酸解(R,S)-3-n-丁基苯酞。最适的有机溶剂、水分活度、转速和转化时间分别是正己烷、0.54、150 r/min和64 h。在此优化条件下,丁基苯酞的转化率为14.8%,产物的对映体过量值为99.3%。 Novozyme 435 can improve enantiomeric selective acidolysis of (R, S)-3-n-butylphthalide. The optimum organic solvent, water activity, agitation velocity and reaction time are hexane,0. 54,150 r/min and 64 h respectively. 14.8 % conversion rate of (R, S)-3-n-butylphthalide and 99.3% enantiomeric excess of product can be obtained under the optimum reaction condition.
出处 《贵州农业科学》 CAS 2007年第6期8-10,14,共4页 Guizhou Agricultural Sciences
基金 国家"973"项目(2003CB716008) 教育部长江学者和创新团队发展计划(IRT0532)
关键词 3-n-丁基苯酞 Novozyme 435 对映体选择性酸解 有机溶剂 水分活度 3-n-butylphthalide Novozyme 435 enantiomeric selective acidolysis organic solvent water activity
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  • 1Barton D H R, Vries J X D. The constitution of sedanolide [J]. Journal of Chemistry Society, 1963(2): 1916-1919.
  • 2MacLeod A J, MacLeod G, Subramanian G. Volatile aroma constituents of celery [ J]. Phytochemistry, 1988, 27 ( 2 ) : 373-375.
  • 3Kitayama T. Microbioal asymmetric synthesis of 3-alkylphthalide derivatives[J]. Tetrahedron Letters, 1997, 8 (22): 3765-3774.
  • 4Zhu X-Z, Li X-Y, Liu J. Recent pharmacological studies on natural products in China[J]. European Journal of Pharmacology, 2004 (500) : 221- 230.
  • 5Soal K, Hori H, Kawahara M. Catalytic enantioselective synthesis of optically active phthalides[J]. Tetrahedron:Asymmetry, 1991, 2(4): 253-254.
  • 6Pedrosa R, Sayaleroy S, Vicente M. A direct efficient diastereoseleetive synthesis of enantiopure 3-substituted-isobenzofuranones[J]. Tetrahedron, 2006(62): 10400-10407.
  • 7Persson M, Costes D, Wehtje E, et al. Effects of solvent, water activity and temperature on lipase and hydroxynltrile lyase enantioselectivity[J]. Enzyme and Microbial Technology, 2002( 30): 916-923.
  • 8Hun C J, Rahman R N Z A, Salleh A B, etal. A newly isolated organic solvent tolerant Bacillus sphaericus 205y producing organic solvent-stable lipase [J]. Biochemical Engineering Journal,2003(15) : 147-151.
  • 9Cernia E, Palocci C, Soro S. The role of the reaction medium in lipase-catalyzed esterificatlons and transesterifications[J]. Chemistry and Physics of Lipids, 1998(93): 157-168.
  • 10Laane C, Boern S, Vos K, et al. Rules for optimization of biocatalysis in organic solvents[J]. Biotechnology and Bioengineering, 1987(30): 81-87.

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  • 1Takase H. Metabolism of diacylglycerol in humans[J].AsiaPacJ Cliff Nutr, 2007, 16 (Suppl 1): 398-403.
  • 2Saito S, Hernandez-Ono A, Ginsberg H N. Dietary 1, 3-diacylglyc- erol protects against diet-induced obesity and insulin resistance[J]. Metabolism, 2007, 56(11): 1566-1575.
  • 3Doucet J I M. Shortening system, products there with and methods for making and using the same: United States Patent, US59098655 [P].1999.
  • 4Maurelli S, Blasi F, Cossignani L, et al. Enzymatic synthesis of struc- tured triacylglycerols containing CLA isomers starting from sn-1, 3- diacylglycerols [J]. J Am Oil Chem Soc, 2009, 86(2): 127-133.
  • 5Scriba G K E. Phenytoin-lipid conjugates as potential prodrug[J]. Arch pharm, 1993, 326:477-481.
  • 6Kihel E I L. Letourueux,synthesis and evalution of anti-inflam- matony[J].Drug Res, 1996,46: 1046-1044.
  • 7Berger M. Regioisomerically pure MAG DAG as synthetical building blooks[J]. Fat Sci Technol, 1993, 95:169-175.
  • 8Wang Y, Zhao M, Ou S,et al. Preparation of a diacylglycerol-en- riched soybean oil by phosphalipase A1 catalyzed hydrolysis[J]. J mol catal B-Enzym, 2009, 56 (2/3): 165-172.
  • 9Holcapek M, Jandera P, Zderadicka P, Hrub6 L. Characterization of triacylglycerol and diacylglycerol composition of plant oils using high-performance liquid chromatography - atmospheric pressure chemical ionization mass spectrometry[J]. J Chromatogra A, 2003, 1010, 195-215.
  • 10Blasi F, Cossignani L, Simonetti M S. Damiani P. Biocatalysed syn- thesis of sn-l,3-diacylglycerol oil from extra virgin olive oil [J]. Enzym Microb Tech, 2007, 41(6/7): 727-732.

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