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Items: 1 to 20 of 131

1.

A novel chemoenzymatic synthesis of propyl caffeate using lipase-catalyzed transesterification in ionic liquid.

Pang N, Gu SS, Wang J, Cui HS, Wang FQ, Liu X, Zhao XY, Wu FA.

Bioresour Technol. 2013 Jul;139:337-42. doi: 10.1016/j.biortech.2013.04.057. Epub 2013 Apr 22.

PMID:
23665696
2.

Rapid synthesis of propyl caffeate in ionic liquid using a packed bed enzyme microreactor under continuous-flow conditions.

Wang J, Gu SS, Cui HS, Yang LQ, Wu XY.

Bioresour Technol. 2013 Dec;149:367-74. doi: 10.1016/j.biortech.2013.09.098. Epub 2013 Sep 29.

PMID:
24128399
3.

Lipophilisation of Caffeic Acid through Esterification with Propanol Using Water-tolerable Acidic Ionic Liquid as Catalyst.

Liu W, Han L.

J Oleo Sci. 2015;64(12):1297-305. doi: 10.5650/jos.ess15136. Epub 2015 Nov 19.

4.

Enzymatic synthesis of caffeic acid phenethyl ester analogues in ionic liquid.

Kurata A, Kitamura Y, Irie S, Takemoto S, Akai Y, Hirota Y, Fujita T, Iwai K, Furusawa M, Kishimoto N.

J Biotechnol. 2010 Jul 20;148(2-3):133-8. doi: 10.1016/j.jbiotec.2010.05.007. Epub 2010 May 27.

PMID:
20553773
5.

A novel continuous flow biosynthesis of caffeic acid phenethyl ester from alkyl caffeate and phenethanol in a packed bed microreactor.

Wang J, Gu SS, Cui HS, Wu XY, Wu FA.

Bioresour Technol. 2014 Apr;158:39-47. doi: 10.1016/j.biortech.2014.01.145. Epub 2014 Feb 10.

PMID:
24583213
6.

Enhanced transesterification of ethyl ferulate with glycerol for preparing glyceryl diferulate using a lipase in ionic liquids as reaction medium.

Sun S, Qin F, Bi Y, Chen J, Yang G, Liu W.

Biotechnol Lett. 2013 Sep;35(9):1449-54. doi: 10.1007/s10529-013-1222-6. Epub 2013 May 21.

PMID:
23690034
7.

Cooperative Reinforcement of Ionic Liquid and Reactive Solvent on Enzymatic Synthesis of Caffeic Acid Phenethyl Ester as an In Vitro Inhibitor of Plant Pathogenic Bacteria.

Xu Y, Sheng S, Liu X, Wang C, Xiao W, Wang J, Wu FA.

Molecules. 2017 Jan 2;22(1). pii: E72. doi: 10.3390/molecules22010072.

8.

A novel method for the synthesis of glyceryl monocaffeate by the enzymatic transesterification and kinetic analysis.

Sun S, Hu B.

Food Chem. 2017 Jan 1;214:192-8. doi: 10.1016/j.foodchem.2016.07.087. Epub 2016 Jul 12.

PMID:
27507465
9.

Highly efficient preparation of lipophilic hydroxycinnamates by solvent-free lipase-catalyzed transesterification.

Weitkamp P, Vosmann K, Weber N.

J Agric Food Chem. 2006 Sep 20;54(19):7062-8.

PMID:
16968063
10.

[Lipase-catalyzed production of biodiesel from high acid value waste oil with ultrasonic assistant].

Wang JX, Huang QD, Huang FH, Wang JW, Huang QJ.

Sheng Wu Gong Cheng Xue Bao. 2007 Nov;23(6):1121-8. Chinese.

PMID:
18257248
11.

Optimized enzymatic synthesis of caffeic acid phenethyl ester by RSM.

Chen HC, Ju HY, Twu YK, Chen JH, Chang CM, Liu YC, Chang C, Shieh CJ.

N Biotechnol. 2010 Feb 28;27(1):89-93. doi: 10.1016/j.nbt.2009.12.002. Epub 2009 Dec 16.

PMID:
20018263
12.

Effect of ionic liquids on enzymatic synthesis of caffeic acid phenethyl ester.

Ha SH, Anh TV, Lee SH, Koo YM.

Bioprocess Biosyst Eng. 2012 Jan;35(1-2):235-40. doi: 10.1007/s00449-011-0601-4. Epub 2011 Sep 10.

PMID:
21909673
13.

Stereoselective synthesis of caffeic acid amides via enzyme-catalyzed asymmetric aminolysis reaction.

Xiao P, Zhang S, Ma H, Zhang A, Lv X, Zheng L.

J Biotechnol. 2013 Dec;168(4):552-9. doi: 10.1016/j.jbiotec.2013.09.004. Epub 2013 Sep 19.

PMID:
24056082
14.

Lipophilic (hydroxy)phenylacetates by solvent-free lipase-catalyzed esterification and transesterification in vacuo.

Weitkamp P, Weber N, Vosmann K.

J Agric Food Chem. 2008 Jul 9;56(13):5083-90. doi: 10.1021/jf8002224. Epub 2008 Jun 10.

PMID:
18540623
15.

Optimization of lipase-catalyzed synthesis of caffeic acid phenethyl ester in ionic liquids by response surface methodology.

Ha SH, Van Anh T, Koo YM.

Bioprocess Biosyst Eng. 2013 Jun;36(6):799-807. doi: 10.1007/s00449-013-0906-6. Epub 2013 Feb 5.

PMID:
23380940
16.

Optimization of lipase-catalyzed biodiesel by isopropanolysis in a continuous packed-bed reactor using response surface methodology.

Chang C, Chen JH, Chang CM, Wu TT, Shieh CJ.

N Biotechnol. 2009 Oct 31;26(3-4):187-92. doi: 10.1016/j.nbt.2009.07.010. Epub 2009 Jul 29.

PMID:
19646554
17.

Ionic liquids as a reaction medium for lipase-catalyzed methanolysis of sunflower oil.

Sunitha S, Kanjilal S, Reddy PS, Prasad RB.

Biotechnol Lett. 2007 Dec;29(12):1881-5. Epub 2007 Jul 19.

PMID:
17634866
18.

New ether-functionalized ionic liquids for lipase-catalyzed synthesis of biodiesel.

Zhao H, Song Z, Olubajo O, Cowins JV.

Appl Biochem Biotechnol. 2010 Sep;162(1):13-23. doi: 10.1007/s12010-009-8717-6. Epub 2009 Jul 26.

PMID:
19633977
19.

Short-chain flavor ester synthesis in organic media by an E. coli whole-cell biocatalyst expressing a newly characterized heterologous lipase.

Brault G, Shareck F, Hurtubise Y, L├ępine F, Doucet N.

PLoS One. 2014 Mar 26;9(3):e91872. doi: 10.1371/journal.pone.0091872. eCollection 2014.

20.

Preparation of lipophilic alkyl (hydroxy)benzoates by solvent-free lipase-catalyzed esterification and transesterification.

Vosmann K, Wiege B, Weitkamp P, Weber N.

Appl Microbiol Biotechnol. 2008 Aug;80(1):29-36. doi: 10.1007/s00253-008-1534-y. Epub 2008 Jun 10.

PMID:
18542947

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