Добірка наукової літератури з теми "Enantioselective hydrolyses"
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Статті в журналах з теми "Enantioselective hydrolyses"
Glänzer, B. I., K. Faber, and H. Griengl. "Enantioselective hydrolyses by baker's yeast - II." Tetrahedron 43, no. 4 (1987): 771–78. http://dx.doi.org/10.1016/s0040-4020(01)90011-0.
Повний текст джерелаTafi, Andrea, Andreas van Almsick, Federico Corelli, Maria Crusco, Kurt E. Laumen, Manfred P. Schneider, and Maurizio Botta. "Computer Simulations of Enantioselective Ester Hydrolyses Catalyzed byPseudomonas cepaciaLipase†." Journal of Organic Chemistry 65, no. 12 (June 2000): 3659–65. http://dx.doi.org/10.1021/jo9919198.
Повний текст джерелаKasai, Masaji, Herman Ziffer, and J. V. Silverton. "Enantioselective ester hydrolyses using Rhizopusnigricans: stereoselective synthesis and absolute stereochemistry of (−)-cis- and (−)-trans-1-hydroxy-4-methyl-1,2,3,4-tetrahydronaphthalene." Canadian Journal of Chemistry 63, no. 6 (June 1, 1985): 1287–91. http://dx.doi.org/10.1139/v85-219.
Повний текст джерелаXie, Zhuo-Feng, Izumi Nakamura, Hiroshi Suemune, and Kiyoshi Sakai. "An insight into the enantioselective hydrolyses of cyclic acetates catalysed by Pseudomonas fluorescens lipase." Journal of the Chemical Society, Chemical Communications, no. 14 (1988): 966. http://dx.doi.org/10.1039/c39880000966.
Повний текст джерелаUtsumi, Ryoichi, Shunsuke Izumi та Toshifumi Hirata. "Enantioselective hydrolyses of α-methylated cyclohexyl acetates by the cultured cells of Marchantia polymorpha". Journal of Molecular Catalysis B: Enzymatic 11, № 4-6 (січень 2001): 439–43. http://dx.doi.org/10.1016/s1381-1177(00)00158-2.
Повний текст джерелаDeardorff, Donald R., Roberto B. Amador, James W. Morton, Henry Y. Kim, Cullen M. Taniguchi, Arnel A. Balbuena, Sam A. Warren, Vadim Fanous, and S. W. Tina Choe. "Chiral induction in cyclopentyl-derived 1,3-meso-diesters: enantioselective hydrolyses with electric eel acetylcholinesterase." Tetrahedron: Asymmetry 10, no. 11 (June 1999): 2139–52. http://dx.doi.org/10.1016/s0957-4166(99)00236-0.
Повний текст джерелаCsuk, René, and Petra Dörr. "Biocatalytical transformations. IV. Enantioselective enzymatic hydrolyses of building blocks for the synthesis of carbocyclic nucleosides." Tetrahedron: Asymmetry 5, no. 2 (January 1994): 269–76. http://dx.doi.org/10.1016/s0957-4166(00)86183-2.
Повний текст джерелаFantin, Giancarlo, Marco Fogagnolo, Alessandra Guerrini, Alessandro Medici, Paola Pedrini, and Silvia Fontana. "Enantioselective hydrolyses with Yarrowia lipolytica: a versatile strain for esters, enol esters, epoxides, and lactones." Tetrahedron: Asymmetry 12, no. 19 (October 2001): 2709–13. http://dx.doi.org/10.1016/s0957-4166(01)00463-3.
Повний текст джерелаGu, Rui-Lin, Ik-Soo Lee, and Charles J. Sih. "Chemo-enzymatic asymmetric synthesis of amino acids. Enantioselective hydrolyses of 2-phenyl-oxazolin-5-ones." Tetrahedron Letters 33, no. 15 (April 1992): 1953–56. http://dx.doi.org/10.1016/0040-4039(92)88111-h.
Повний текст джерелаMartinez-Rodríguez, Sergio, Rafael Contreras-Montoya, Jesús M. Torres, Luis Álvarez de Cienfuegos, and Jose Antonio Gavira. "A New L-Proline Amide Hydrolase with Potential Application within the Amidase Process." Crystals 12, no. 1 (December 23, 2021): 18. http://dx.doi.org/10.3390/cryst12010018.
Повний текст джерелаДисертації з теми "Enantioselective hydrolyses"
Kerry, Simon. "Investigation of enantioselective hydrolyses with fungal hydrolase systems." Thesis, Loughborough University, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.329713.
Повний текст джерелаBeard, Timothy Mark. "Enzyme catalysed hydrolysis of nitriles and amides." Thesis, University of Huddersfield, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.363237.
Повний текст джерелаHussain, Sajad. "Enantioselective hydrolysis of phenylglycineamide to phenylglycine by Rhodococcus NP3854." Thesis, Keele University, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.288510.
Повний текст джерелаChauveau, Viriot Christine. "Synthèse de dérivés 3-aryloxypropioniques en mélange racémique et sous forme enantiomeriquement pure : utilisation dans la préparation de quelques hétérocycles." Nancy 1, 1991. http://www.theses.fr/1991NAN10132.
Повний текст джерелаNelson, Keegan Gregory. "Enantioselective hydrolysis of 1-arylpropargylic esters by enzymatic kinetic resolution and dynamic kinetic resolution of 1-arylallylic esters." Thesis, University of Missouri - Kansas City, 2013. http://pqdtopen.proquest.com/#viewpdf?dispub=1538847.
Повний текст джерелаChiral 1-arylprop-2-en-1-ols and 1-arylprop-2-yn-1-ols are useful building blocks for modern pharmaceuticals. Previous work has found that enzyme catalysis is a potential new enantioselective synthetic route to the former. We found that Candida antarctica lipase is also an effective catalyst for kinetic resolution of various substituted 1 arylpropargylic acetates and haloacetates, affording the respective (R) -1 arylproargylic alcohols with high enantioselectivity (99-100% ee). By varying the substituents on both sides of the ester bond, we discovered that the deacylation of lipase is likely the rate-determining step for our catalytic system. A greater challenge is designing a dynamic kinetic resolution (DKR) system for such substrates, which combines a resolving catalyst (lipase) with a racemizing catalyst, and can potentially lead to quantitative conversion of a racemic substrate into an enantiopure product. We studied the efficacy of various transition-metal complexes for substrate racemization and will report our results for In and Cu compounds.
While kinetic resolution has been performed on the 1-arylallylic acetates with excellent yield and enantioselectivity and the DKR regime has been designed, the resulting site-isolation system has required further testing and fine tuning. We have herein investigated the utilization of macroscale site-isolation as well as various factors including solvent, and acyl donor effects in order to optimize conditions of the system.
Miao, Lei. "Synthesis of Amphibian Alkaloids and Development of Acetaminophen Analogues." ScholarWorks@UNO, 2009. http://scholarworks.uno.edu/td/985.
Повний текст джерелаКниги з теми "Enantioselective hydrolyses"
Kerry, Simon. Investigation of enantioselective hydrolyses with fungal hydrolase systems. 1989.
Знайти повний текст джерелаЧастини книг з теми "Enantioselective hydrolyses"
Smeets, J. W. H., and A. P. G. Kieboom. "Enzymatic enantioselective ester hydrolysis by carboxylesterase NP." In Microbial Reagents in Organic Synthesis, 273–88. Dordrecht: Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-2444-7_22.
Повний текст джерелаBodanszky, Miklos, and Agnes Bodanszky. "Synthesis and Enantioselective Enzymic Hydrolysis of Tetraalanine [1]." In The Practice of Peptide Synthesis, 191–92. Berlin, Heidelberg: Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-85055-4_30.
Повний текст джерелаRiefling, B. F., W. K. Brümmer, and H. J. Gais. "Enantioselective Ple-Catalyzed Hydrolysis of Meso-Dimethyl Tetrahydrophthalate on a 100 Mole Scale — Protection of the Enzyme by Addition of Bovine Serum Albumin." In Enzymes as Catalysts in Organic Synthesis, 347. Dordrecht: Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-009-4686-6_22.
Повний текст джерелаTaber, Douglass. "Enantioselective Assembly of Oxygenated Stereogenic Centers." In Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0032.
Повний текст джерелаTaber, Douglass F. "The Tanino Synthesis of (-)-Glycinoeclepin A." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0095.
Повний текст джерелаTaber, Douglass F. "Enantioselective Construction of Alkylated Centers: The Shishido Synthesis of (+)-Helianane." In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0038.
Повний текст джерелаTaber, Douglass. "Transition Metal Catalyzed Construction of Carbocyclic Rings: (-)-Hamigeran B." In Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0076.
Повний текст джерелаTaber, Douglass F. "Organocatalytic C–C Ring Construction: Prostaglandin F2α (Aggarwal)." In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0072.
Повний текст джерелаTaber, Douglass F. "Construction of Oxygenated and Aminated Stereogenic Centers." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0037.
Повний текст джерелаOlejniczak, Teresa, and Czesŀaw Wawrzeńczyk. "Lactones 8. [1] Enantioselective hydrolysis of γ-acetoxy-δ-lactones." In Studies in Surface Science and Catalysis, 3387–92. Elsevier, 2000. http://dx.doi.org/10.1016/s0167-2991(00)80546-7.
Повний текст джерелаТези доповідей конференцій з теми "Enantioselective hydrolyses"
Sato, Letícia, Paulo José Samenho Moran, Lucidio Cristovão Fardelone, and José Augusto Rosário Rodrigues. "Screening of Lipases for Enantioselective Hydrolysis of 1-butiryloxyarylphosphonates." In XXIV Congresso de Iniciação Científica da UNICAMP - 2016. Campinas - SP, Brazil: Galoa, 2016. http://dx.doi.org/10.19146/pibic-2016-51226.
Повний текст джерелаGao, Shengbo, Quanhui Li, Tingting Yao, Zhengyang Wang, Luoyun Zheng, and Jiaying Xin. "Lipase Catalyzed Naproxen Methyl Ester Enantioselective Hydrolysis in Ionic Liquids." In 2016 6th International Conference on Mechatronics, Computer and Education Informationization (MCEI 2016). Paris, France: Atlantis Press, 2016. http://dx.doi.org/10.2991/mcei-16.2016.4.
Повний текст джерелаZhang, Chensheng, Zhijun Zhang, Chunxiu Li, Huilei Yu, and Jianhe Xu. "Enantioselective Hydrolysis of O-Chloromandelonitrile by Novel Arylacetonitrilase Mined from Gene Database." In 14th Asia Pacific Confederation of Chemical Engineering Congress. Singapore: Research Publishing Services, 2012. http://dx.doi.org/10.3850/978-981-07-1445-1_324.
Повний текст джерелаSANTOS DE OLIVEIRA, PRISCILA, Paulo José Samenho Moran, Lucidio Cristovão Fardelone, and José Augusto Rosário Rodrigues. "Enantioselective Hydrolysis of 1-Aryl-2-chloroethyl propanoate Mediated by Burkholderia cepacia and Candida rugosa Lipases." In XXIV Congresso de Iniciação Científica da UNICAMP - 2016. Campinas - SP, Brazil: Galoa, 2016. http://dx.doi.org/10.19146/pibic-2016-50943.
Повний текст джерела