Статті в журналах з теми "Enantioselective hydrolyses"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Enantioselective hydrolyses".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Переглядайте статті в журналах для різних дисциплін та оформлюйте правильно вашу бібліографію.
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 джерелаCharton, Marvin, and Herman Ziffer. "Contributions of steric, electrical, and polarizability effects in enantioselective hydrolyses with Rhizopus nigricans: a quantitative analysis." Journal of Organic Chemistry 52, no. 12 (June 1987): 2400–2403. http://dx.doi.org/10.1021/jo00388a012.
Повний текст джерелаGU, R. L., I. S. LEE, and C. J. SIH. "ChemInform Abstract: Chemo-Enzymatic Asymmetric Synthesis of Amino Acids. Enantioselective Hydrolyses of 2-Phenyloxazolin-5-ones." ChemInform 23, no. 41 (August 21, 2010): no. http://dx.doi.org/10.1002/chin.199241230.
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. "ChemInform Abstract: Chiral Induction in Cyclopentyl-Derived 1,3-meso-Diesters: Enantioselective Hydrolyses with Electric Eel Acetylcholinesterase." ChemInform 30, no. 48 (June 12, 2010): no. http://dx.doi.org/10.1002/chin.199948046.
Повний текст джерелаFantin, Giancarlo, Marco Fogagnolo, Alessandra Guerrini, Alessandro Medici, Paola Pedrini, and Silvia Fontana. "ChemInform Abstract: Enantioselective Hydrolyses with Yarrowia lipolytica: A Versatile Strain for Esters, Enol Esters, Epoxides, and Lactones." ChemInform 33, no. 22 (May 21, 2010): no. http://dx.doi.org/10.1002/chin.200222036.
Повний текст джерелаCSUK, R., and P. DOERR. "ChemInform Abstract: Biocatalytical Transformations. Part 4. Enantioselective Enzymatic Hydrolyses of Building Blocks for the Synthesis of Carbocyclic Nucleosides." ChemInform 25, no. 28 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199428066.
Повний текст джерелаBanerjee, Anirban, Praveen Kaul, Rohit Sharma, and U. C. Banerjee. "A High-Throughput Amenable Colorimetric Assay for Enantioselective Screening of Nitrilase-Producing Microorganisms Using pH Sensitive Indicators." Journal of Biomolecular Screening 8, no. 5 (October 2003): 559–65. http://dx.doi.org/10.1177/1087057103256910.
Повний текст джерелаNaemura, Koichiro, Nobuo Takahashi, Shunsuke Tanaka, Michi Ueno, and Hiroaki Chikamatsu. "Enzyme-Catalyzed Enantioselective and Regioselective Hydrolyses of (2RS,7SR)-2,7-Diacetoxybicyclo[2.2.1]heptane and (2RS,7RS)-2,7-Diacetoxybicydo[2.2.1]heptane." Bulletin of the Chemical Society of Japan 63, no. 4 (April 1990): 1010–14. http://dx.doi.org/10.1246/bcsj.63.1010.
Повний текст джерелаGlänzer, B. I., K. Faber, and H. Griengl. "Enantioselective hydrolyses by baker's yeast - III11For part II Bee; B.I. Glänzer, K. Faber and H. Griengl, Tetrahedron 43, 771 (1987)." Tetrahedron 43, no. 24 (1987): 5791–96. http://dx.doi.org/10.1016/s0040-4020(01)87785-1.
Повний текст джерелаZhang, Yan, Jiang Pan, Zheng-Jiao Luan, Guo-Chao Xu, Sunghoon Park, and Jian-He Xu. "Cloning and Characterization of a Novel Esterase from Rhodococcus sp. for Highly Enantioselective Synthesis of a Chiral Cilastatin Precursor." Applied and Environmental Microbiology 80, no. 23 (September 19, 2014): 7348–55. http://dx.doi.org/10.1128/aem.01597-14.
Повний текст джерелаChen, X. J., A. Archelas, and R. Furstoss. "Microbiological transformations. 27. The first examples for preparative-scale enantioselective or diastereoselective epoxide hydrolyses using microorganisms. An unequivocal access to all four bisabolol stereoisomers." Journal of Organic Chemistry 58, no. 20 (September 1993): 5528–32. http://dx.doi.org/10.1021/jo00072a043.
Повний текст джерелаARAND, Michael, Frank MÜLLER, Astrid MECKY, Willy HINZ, Phillipe URBAN, Denis POMPON, Roland KELLNER, and Franz OESCH. "Catalytic triad of microsomal epoxide hydrolase: replacement of Glu404 with Asp leads to a strongly increased turnover rate." Biochemical Journal 337, no. 1 (December 17, 1998): 37–43. http://dx.doi.org/10.1042/bj3370037.
Повний текст джерелаCHEN, X. J., A. ARCHELAS, and R. FURSTOSS. "ChemInform Abstract: Microbiological Transformations. Part 27. The First Examples for Preparative-Scale Enantioselective or Diastereoselective Epoxide Hydrolyses Using Microorganisms. An Unequivocal Access to All Four Bisabolol Stereoisomers." ChemInform 25, no. 7 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199407058.
Повний текст джерелаTang, Feng Xiang, Yun Bo Li, Chun Meng, and Xue Qing Zhao. "A Two-Step Resolution for Preparing Enantiopure (S)-Ethyl Nipecotate." Advanced Materials Research 393-395 (November 2011): 559–66. http://dx.doi.org/10.4028/www.scientific.net/amr.393-395.559.
Повний текст джерелаMajewska, Paulina. "Lipase-Catalyzed Kinetic Resolution of Dimethyl and Dibutyl 1-Butyryloxy-1-carboxymethylphosphonates." Catalysts 11, no. 8 (August 10, 2021): 956. http://dx.doi.org/10.3390/catal11080956.
Повний текст джерелаLoandos, María del H., Ana C. Muro, Margarita B. Villecco, Marcelo F. Masman, Paul G. M. Luiten, Sebastian A. Andujar, Fernando D. Suvire, and Ricardo D. Enriz. "Catalytic and Molecular Properties of Rabbit Liver Carboxylesterase Acting on 1,8-Cineole Derivatives." Natural Product Communications 7, no. 9 (September 2012): 1934578X1200700. http://dx.doi.org/10.1177/1934578x1200700901.
Повний текст джерелаChênevert, Robert, and Martin Létourneau. "Enantioselectivity of carbonic anhydrase catalyzed hydrolysis of mandelic methyl esters." Canadian Journal of Chemistry 68, no. 2 (February 1, 1990): 314–16. http://dx.doi.org/10.1139/v90-044.
Повний текст джерелаLeśniarek, Aleksandra, Anna Chojnacka, and Witold Gładkowski. "Application of Lecitase® Ultra-Catalyzed Hydrolysis to the Kinetic Resolution of (E)-4-phenylbut-3-en-2-yl Esters." Catalysts 8, no. 10 (September 28, 2018): 423. http://dx.doi.org/10.3390/catal8100423.
Повний текст джерелаLoandos, María del H., Margarita B. Villecco, Eleuterio Burgueño-Tapia, Pedro Joseph-Nathan, and César A. N. Catalán. "Preparation and Absolute Configuration of (1R,4R)-(+)-3-Oxo-, (1S,4S)-(-)-3-Oxo- and (1R,3S,4R)-(+)-3-Acetyloxy-5-oxo-1,8-cineole." Natural Product Communications 4, no. 11 (November 2009): 1934578X0900401. http://dx.doi.org/10.1177/1934578x0900401116.
Повний текст джерелаTrott, Sandra, Sibylle Bürger, Carsten Calaminus, and Andreas Stolz. "Cloning and Heterologous Expression of an Enantioselective Amidase from Rhodococcus erythropolis Strain MP50." Applied and Environmental Microbiology 68, no. 7 (July 2002): 3279–86. http://dx.doi.org/10.1128/aem.68.7.3279-3286.2002.
Повний текст джерелаJammer, S., D. Rizkov, F. Gelman, and O. Lev. "Quantitative structure–activity relationship correlation between molecular structure and the Rayleigh enantiomeric enrichment factor." Environmental Science: Processes & Impacts 17, no. 8 (2015): 1370–76. http://dx.doi.org/10.1039/c5em00084j.
Повний текст джерелаT. Mohd Ali, M., and . "Synthesis of -Hydroxy -Proline: Potential for Organocataly-sis Reactions." International Journal of Engineering & Technology 7, no. 4.14 (December 24, 2019): 237. http://dx.doi.org/10.14419/ijet.v7i4.14.27571.
Повний текст джерелаSinha, Subhash C., Ehud Keinan, and Jean Louis Reymond. "Antibody-catalyzed enantioselective epoxide hydrolysis." Journal of the American Chemical Society 115, no. 11 (June 1993): 4893–94. http://dx.doi.org/10.1021/ja00064a061.
Повний текст джерелаGlänzer, B. I., K. Faber, and H. Griengl. "Enantioselective hydrolysis by baker's yeast." Tetrahedron Letters 27, no. 36 (1986): 4293–94. http://dx.doi.org/10.1016/s0040-4039(00)94256-4.
Повний текст джерелаLiu, Xue Ying, Hong Yan Zeng, Deng Hong Peng, Bi Foua Claude Alain Gohi, Qing Jun Huang, Chao Yu, and Yu Qin Li. "Molecular Docking Studies on the Interaction of 2-Arylpropionate Esters with Candida rugosa Lipase." Applied Mechanics and Materials 496-500 (January 2014): 520–23. http://dx.doi.org/10.4028/www.scientific.net/amm.496-500.520.
Повний текст джерелаJin, Jian Zhong, and Jie Zhang. "Highly Enantioselective Hydrolysis of Racemic Isopropyl Tert-Leucinate by Newly Discovered Baclicus Lincheniformis Jx010 for Synthesis of L-Tert-Butyl Leucine." Advanced Materials Research 343-344 (September 2011): 453–56. http://dx.doi.org/10.4028/www.scientific.net/amr.343-344.453.
Повний текст джерелаToone, Eric J., and J. Bryan Jones. "Enzymes in organic synthesis. 40. Evaluation of the enantioselectivity of the pig liver esterase catalyzed hydrolyses of racemic piperidine carboxylic acid esters." Canadian Journal of Chemistry 65, no. 12 (December 1, 1987): 2722–26. http://dx.doi.org/10.1139/v87-452.
Повний текст джерелаMatsumoto, Takashi, Mio Ochiai, Yuki Akisawa та Daichi Kajiyama. "Desymmetrization of σ-Symmetric Biphenyl-2,6-diyl Diacetate Derivatives by Lipase-Catalyzed Hydrolysis: Unexpected Effect of C(3′)-Substituent on the Enantiotopic Group Selectivity". Synlett 30, № 05 (4 січня 2019): 557–62. http://dx.doi.org/10.1055/s-0037-1611701.
Повний текст джерелаMączka, Wanda K., and Agnieszka Mironowicz. "Enantioselective Hydrolysis of Bromo- and Methoxy-Substituted 1-Phenylethanol Acetates Using Carrot and Celeriac Enzymatic Systems." Zeitschrift für Naturforschung C 62, no. 5-6 (June 1, 2007): 397–402. http://dx.doi.org/10.1515/znc-2007-5-613.
Повний текст джерелаShen, Duan, Jian-He Xu, Peng-Fei Gong, Hui-Yuan Wu, and You-Yan Liu. "Isolation of an esterase-producing Trichosporon brassicae and its catalytic performance in kinetic resolution of ketoprofen." Canadian Journal of Microbiology 47, no. 12 (December 1, 2001): 1101–6. http://dx.doi.org/10.1139/w01-121.
Повний текст джерелаRoura Padrosa, David, Valerio De Vitis, Martina Contente, Francesco Molinari, and Francesca Paradisi. "Overcoming Water Insolubility in Flow: Enantioselective Hydrolysis of Naproxen Ester." Catalysts 9, no. 3 (March 3, 2019): 232. http://dx.doi.org/10.3390/catal9030232.
Повний текст джерелаGadler, P., S. M. Glueck, W. Kroutil, B. M. Nestl, B. Larissegger-Schnell, B. T. Ueberbacher, S. R. Wallner, and K. Faber. "Biocatalytic approaches for the quantitative production of single stereoisomers from racemates." Biochemical Society Transactions 34, no. 2 (March 20, 2006): 296–300. http://dx.doi.org/10.1042/bst0340296.
Повний текст джерелаPogorevc, Mateja, and Kurt Faber. "Purification and Characterization of an Inverting Stereo- and Enantioselective sec-Alkylsulfatase from the Gram-Positive Bacterium Rhodococcus ruber DSM 44541." Applied and Environmental Microbiology 69, no. 5 (May 2003): 2810–15. http://dx.doi.org/10.1128/aem.69.5.2810-2815.2003.
Повний текст джерелаSerreqi, Alessio N., and Romas J. Kazlauskas. "Kinetic resolution of sulfoxides with pendant acetoxy groups using cholesterol esterase: substrate mapping and an empirical rule for chiral phenols." Canadian Journal of Chemistry 73, no. 8 (August 1, 1995): 1357–67. http://dx.doi.org/10.1139/v95-167.
Повний текст джерелаMatsumoto, Kazutsugu, Masaki Nogawa, Megumi Shimojo, Hiromichi Ohta, and Minoru Hatanaka. "Enantioselective Microbial Hydrolysis of Disubstituted Cyclic Carbonates." HETEROCYCLES 68, no. 7 (2006): 1329. http://dx.doi.org/10.3987/com-06-10765.
Повний текст джерелаChĕnevert, Robert, Roxane Pouliot, and Patrick Bureau. "Enantioselective hydrolysis of (±)-chloramphenicol palmitate by hydrolases." Bioorganic & Medicinal Chemistry Letters 4, no. 24 (December 1994): 2941–44. http://dx.doi.org/10.1016/s0960-894x(01)80844-1.
Повний текст джерелаOlejniczak, Teresa, та Zbigniew Ciunik. "Enantioselective hydrolysis of δ-acetoxy-γ-lactones". Tetrahedron: Asymmetry 15, № 23 (листопад 2004): 3743–49. http://dx.doi.org/10.1016/j.tetasy.2004.10.023.
Повний текст джерелаBredikhina, Z. A., V. G. Novikova, and A. A. Bredikhin. "Jacobsen Enantioselective Hydrolysis of Glycidyl Diethyl Phosphate." Russian Journal of General Chemistry 75, no. 10 (October 2005): 1514–16. http://dx.doi.org/10.1007/s11176-005-0460-2.
Повний текст джерелаSellergren, Börje, and Kenneth J. Shea. "Enantioselective ester hydrolysis catalyzed by imprinted polymers." Tetrahedron: Asymmetry 5, no. 8 (August 1994): 1403–6. http://dx.doi.org/10.1016/0957-4166(94)80096-0.
Повний текст джерелаMatsumoto, K., M. Okudomi, K. Ageishi, T. Yamada, N. Chihara, T. Nakagawa, and K. Mizuochi. "Enantioselective Hydrolysis of Soluble Polymer-Supported Carboxylates." Synfacts 2010, no. 12 (November 22, 2010): 1443. http://dx.doi.org/10.1055/s-0030-1258913.
Повний текст джерелаSmeets, J. W. H., and A. P. G. Kieboom. "Enzymatic enantioselective ester hydrolysis by carboxylesterase NP." Recueil des Travaux Chimiques des Pays-Bas 111, no. 11 (September 2, 2010): 490–95. http://dx.doi.org/10.1002/recl.19921111104.
Повний текст джерела