Gotowa bibliografia na temat „Benzaldehyde”
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Artykuły w czasopismach na temat "Benzaldehyde"
Shaw, J. P., F. Schwager i S. Harayama. "Substrate-specificity of benzyl alcohol dehydrogenase and benzaldehyde dehydrogenase encoded by TOL plasmid pWW0. Metabolic and mechanistic implications". Biochemical Journal 283, nr 3 (1.05.1992): 789–94. http://dx.doi.org/10.1042/bj2830789.
Pełny tekst źródłaChalmers, R. M., i C. A. Fewson. "Purification and characterization of benzaldehyde dehydrogenase I from Acinetobacter calcoaceticus". Biochemical Journal 263, nr 3 (1.11.1989): 913–19. http://dx.doi.org/10.1042/bj2630913.
Pełny tekst źródłaHandayani, Sri, Sunarto, Sunarto, i Susila Kristianingrum. "OPTIMIZATION OF TIME REACTION AND HYDROXIDE ION CONCENTRATION ON FLAVONOID SYNTHESIS FROM BENZALDEHYDE AND ITS DERIVATIVES". Indonesian Journal of Chemistry 5, nr 2 (14.06.2010): 163–68. http://dx.doi.org/10.22146/ijc.21825.
Pełny tekst źródłaYoung, Jay A. "Benzaldehyde". Journal of Chemical Education 82, nr 12 (grudzień 2005): 1770. http://dx.doi.org/10.1021/ed082p1770.
Pełny tekst źródłaHuyen, Nga Hoang, Ulrike Jannsen, Hanaa Mansour i Norbert Jux. "Introducing the Staudinger phosphazene reaction to porphyrin chemistry". Journal of Porphyrins and Phthalocyanines 08, nr 12 (grudzień 2004): 1356–65. http://dx.doi.org/10.1142/s1088424604000714.
Pełny tekst źródłaIto, Satoru, Yoshihiro Kon, Takuya Nakashima, Dachao Hong, Hideo Konno, Daisuke Ino i Kazuhiko Sato. "Titania-Catalyzed H2O2 Thermal Oxidation of Styrenes to Aldehydes". Molecules 24, nr 14 (10.07.2019): 2520. http://dx.doi.org/10.3390/molecules24142520.
Pełny tekst źródłaGuo, Huan-Mei. "Benzaldehyde propionylhydrazone". Acta Crystallographica Section E Structure Reports Online 63, nr 9 (10.08.2007): o3787. http://dx.doi.org/10.1107/s1600536807038925.
Pełny tekst źródłaKong, Lingqian, Yan Qiao, Ji-Dong Zhang i Xiu-Ping Ju. "Benzaldehyde thiosemicarbazone". Acta Crystallographica Section E Structure Reports Online 64, nr 12 (22.11.2008): o2412. http://dx.doi.org/10.1107/s1600536808038270.
Pełny tekst źródłaChen, Minqi, Jinyue Liang, Yi Liu, Yayue Liu, Chunxia Zhou, Pengzhi Hong, Yi Zhang i Zhong-Ji Qian. "The Mechanism of Two Benzaldehydes from Aspergillus terreus C23-3 Improve Neuroinflammatory and Neuronal Damage to Delay the Progression of Alzheimer’s Disease". International Journal of Molecular Sciences 24, nr 2 (4.01.2023): 905. http://dx.doi.org/10.3390/ijms24020905.
Pełny tekst źródłaChen, Kuang-Yao, Yi-Ju Chen, Chien-Ju Cheng, Kai-Yuan Jhan i Lian-Chen Wang. "Benzaldehyde Attenuates the Fifth Stage Larval Excretory–Secretory Product of Angiostrongylus cantonensis-Induced Injury in Mouse Astrocytes via Regulation of Endoplasmic Reticulum Stress and Oxidative Stress". Biomolecules 12, nr 2 (21.01.2022): 177. http://dx.doi.org/10.3390/biom12020177.
Pełny tekst źródłaRozprawy doktorskie na temat "Benzaldehyde"
Yilgor, Pinar. "Bioprocess Operation Parameters For Benzaldehyde Lyase Production". Master's thesis, METU, 2004. http://etd.lib.metu.edu.tr/upload/3/12605242/index.pdf.
Pełny tekst źródłaN=250, 375, 500, 625, 750 min-1 and at QO/VR=0.7 vvm, N=750 min-1 conditions. The highest cell concentration and benzaldehyde lyase activity were obtained at 0.5 vvm, 500 min-1 condition as 2.3 kg m-3 and 860 U cm-3, respectively. Finally, the effect of pH was investigated for benzaldehyde lyase production process at Qo/VR=0.5 vvm, N=500 min-1 condition, at pHC=5.0, 6.4, 6.7, 7.0, 7.2 and 7.8 values. Among the investigated pH values, the highest cell concentration and enzyme activity were obtained at pHC=7.0 condition as 2.1 kg m-3
775 U cm-3. However, the values obtained at this condition, were lower than the values obtained at pHUC=7.2 uncontrolled pH operation. Hence, medium oxygen transfer condition and uncontrolled pH operation are found to be favorable for benzaldehyde lyase production.
Simsek, Ilke. "Benzaldehyde Lyase Catalyzed Synthesis Of Novel Acyloins". Master's thesis, METU, 2009. http://etd.lib.metu.edu.tr/upload/12610901/index.pdf.
Pełny tekst źródła#945
-Hydroxy phosphonates are versatile building blocks for the synthesis of many biologically active compounds that display antiviral, antibacterial, anticancer, pesticide activities beside their enzyme inhibitory activities such as they are the inhibitors of rennin or human immunodeficiency virus (HIV) protease and polymerase. Benzaldehyde lyase is able to catalyze not only C-C bond formation reactions but also C-C bond breaking reactions with high enantioselectivity that brings about the development of new synthetic methodologies for the synthesis of hydroxy ketones which are the key intermediates in the synthesis of many biologically active compounds due to the versatility of stereogenic center for developing structural diversity. There are several synthetic methodologies for the synthesis of hydroxy phoshonates however, in this work we have achieved the synthesis of hydroxy phoshonates through C-C bond forming reactions catalyzed by Benzaldehyde lyase that offers the use of green methodologies. Moreover, we have achieved the synthesis of hydroxy ketones which are versatile building blocks in the synthesis of many biologically active compounds via the immobilization of BAL enzyme on superparamagnetic solid support with high yield and high enantioselectivity.
Mackintosh, Robert William. "Benzyl alcohol dehydrogenase and benzaldehyde dehydrogenase of Acinetobacter calcoaceticus". Thesis, University of Glasgow, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.281219.
Pełny tekst źródłaSimmonds, Julie. "Production of benzaldehyde by biotransformation using Pseudomonas putida ATCC 12633". Thesis, University of Kent, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.244331.
Pełny tekst źródłaBoyle, Sarah Ann. "Oxidation of toluene". Thesis, Queen's University Belfast, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.387977.
Pełny tekst źródłaSmith, Derek John. "Femtosecond Laser Mass Spectrometry (FLMS)". Thesis, University of Glasgow, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.264149.
Pełny tekst źródłaLevent, Hande. "Feeding Strategy Development For Benzaldehyde Lyase Production By Recombinant Escherichia Coli Bl21". Master's thesis, METU, 2008. http://etd.lib.metu.edu.tr/upload/3/12609596/index.pdf.
Pełny tekst źródłaand the highest cell concentration and benzaldehyde lyase activity were obtained as CX=5.3 kg m-3 and A=1617 U cm-3, respectively, in the medium containing 7.5 kg m-3 glucose and 7.5 kg m-3 fructose. Then, different feeding strategies were developed to produce efficient cells with high concentration and BAL activity. In the first strategy, after 10 hours of batch-cultivation with molasses based medium having 7.5 kg m-3 glucose and 7.5 kg m-3 fructose concentration, based on the airflow rate, pretreated molasses was fed to the system. When air flow rate decreased considerably, fed was given to the system that results in increase in glucose and fructose concentration in the medium to 2.5 kg m-3. At the end of the process, the highest cell concentration obtained was CX=7.4 kg m-3. The maximum activity was reached at 20th hour as A=2360 U cm-3. On the other hand, as air flow variation only demonstrated the absence of glucose not fructose, a second strategy, based on the detection of the fructose and glucose concentrations during the process, was applied. In this strategy when glucose and fructose were depleted, fed was given to the system that results in increase in glucose and fructose concentration in the medium to 2.5 kg m-3
and the highest BAL activity was obtained as 2370 U cm-3 at t= 26 h where the cell concentration was 7.5 kg m-3. At the last strategy, when glucose and fructose were depleted, fed was given to the system that results in increase in CGlucose=1.5 kg m-3 and CFructose=1.5 kg m-3 in the production medium to decrease the accumulation of acetic acid. By this strategy highest cell concentration was obtained as 8.04 kg m-3 at t=24 h and the highest BAL activity was 2315 U cm-3. These strategies could be accepted having the same BAL activity with little distinctions. However, cell concentration of the last one was higher than others and also the lowest amount of carbon source was used. Thus, last one could be chosen as the most favorable strategy.
Taspinar, Hatice. "Exponential Feeding Strategy Development For Benzaldehyde Lyase Production By Recombinant Escherichia Coli". Master's thesis, METU, 2010. http://etd.lib.metu.edu.tr/upload/12612311/index.pdf.
Pełny tekst źródłaJones, Rheinallt M. "The catabolism of aromatic esters by Acinetobacter sp. ADP1". Thesis, Bangor University, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.322563.
Pełny tekst źródłaGuena, Thierry. "Electrochemistry of aryl carbonyl compounds in flow cells". Thesis, University of Southampton, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.243180.
Pełny tekst źródłaKsiążki na temat "Benzaldehyde"
Kagaku Busshitsu Hyōka Kenkyū Kikō i Shin Enerugī Sangyō Gijutsu Sōgō Kaihatsu Kikō (Japan), red. Benzuarudehido: Benzaldehyde. Tōkyō: Seihin Hyōka Gijutsu Kiban Kikō Kagaku Busshitsu Hyōka Kenkyū Kikō, 2009.
Znajdź pełny tekst źródłaKagaku Busshitsu Hyōka Kenkyū Kikō i Shin Enerugī Sangyō Gijutsu Sōgō Kaihatsu Kikō (Japan), red. Benzuarudehido: Benzaldehyde. Tōkyō: Seihin Hyōka Gijutsu Kiban Kikō Kagaku Busshitsu Hyōka Kenkyū Kikō, 2009.
Znajdź pełny tekst źródłaStillger, Thomas. Enantioselektive C-C Knüpfung mit Enzymen: Charakterisierung und reaktionstechnische Bearbeitung der Benzaldehydlyase aus Pseudomonas fluorescens Biovar I. Jülich: Forschungszentrum Jülich GmbH, Zentralbibliothek, 2006.
Znajdź pełny tekst źródłaBishop, Jack. NTP technical report on the toxicology and carcinogenesis studies of benzaldehyde (CAS no. 100-52-7) in F344/N rats and B6C3F1 mice (gavage studies). Research Triangle Park, NC: U.S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, 1990.
Znajdź pełny tekst źródłaCzęści książek na temat "Benzaldehyde"
Bährle-Rapp, Marina. "Benzaldehyde". W Springer Lexikon Kosmetik und Körperpflege, 62. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_1073.
Pełny tekst źródłaGooch, Jan W. "Benzaldehyde". W Encyclopedic Dictionary of Polymers, 73. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_1205.
Pełny tekst źródłaSchomburg, Dietmar, Margit Salzmann i Dörte Stephan. "Benzaldehyde dehydrogenase (NAD+)". W Enzyme Handbook, 139–42. Berlin, Heidelberg: Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-58051-2_26.
Pełny tekst źródłaSchomburg, Dietmar, Margit Salzmann i Dörte Stephan. "Benzaldehyde dehydrogenase (NADP+)". W Enzyme Handbook, 39–41. Berlin, Heidelberg: Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-58051-2_6.
Pełny tekst źródłaVogt, J. "648 C7H6O Benzaldehyde". W Asymmetric Top Molecules. Part 3, 130–32. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-14145-4_70.
Pełny tekst źródłaHirota, E., K. Kuchitsu, T. Steimle, J. Vogt i N. Vogt. "118 C7H6O Benzaldehyde". W Molecules Containing Three or Four Carbon Atoms and Molecules Containing Five or More Carbon Atoms, 291–92. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-41504-3_249.
Pełny tekst źródłaWohlfarth, Ch. "Viscosity of benzaldehyde". W Supplement to IV/18, 439. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_242.
Pełny tekst źródłaWohlfarth, Christian. "Viscosity of benzaldehyde". W Viscosity of Pure Organic Liquids and Binary Liquid Mixtures, 268. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49218-5_243.
Pełny tekst źródłaWohlfarth, Christian. "Refractive index of benzaldehyde". W Optical Constants, 284. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49236-9_268.
Pełny tekst źródłaHolze, Rudolf. "Ionic conductivities of benzaldehyde". W Electrochemistry, 261. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49251-2_244.
Pełny tekst źródłaStreszczenia konferencji na temat "Benzaldehyde"
Bagnich, Sergey A. "Phosphorescence of benzaldehyde in porous glasses". W Tunable Solid State Lasers, redaktorzy Wieslaw Strek, Edward Lukowiak i Barbara Nissen-Sobocinska. SPIE, 1997. http://dx.doi.org/10.1117/12.293449.
Pełny tekst źródłaZhang, Bin-Liang, Lu-Jie Cao, Shan Xu i Ping Wang. "Synthesis of 4-(pyrrolidin-1-ylmethyl)benzaldehyde". W 2017 2nd International Conference on Biological Sciences and Technology (BST 2017). Paris, France: Atlantis Press, 2018. http://dx.doi.org/10.2991/bst-17.2018.37.
Pełny tekst źródłaTouati, Yousseuf, Mohammed Benabdallah, Julio A. Seijas, Noureddine Choukchou-Braham i M. Pilar Vázquez-Tato. "Reactivity of 2-aminothiazole with benzaldehyde and malononitrile". W The 23rd International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2019. http://dx.doi.org/10.3390/ecsoc-23-06699.
Pełny tekst źródłaBagnich, Sergey A. "Migration of benzaldehyde triplet-excitation in porous matrices". W Tunable Solid State Lasers, redaktorzy Wieslaw Strek, Edward Lukowiak i Barbara Nissen-Sobocinska. SPIE, 1997. http://dx.doi.org/10.1117/12.293450.
Pełny tekst źródłaDuan, Yongli, Zhimin Li, Qidong Tang, Rui Li i Shan Xu. "Synthesis of 2 - ((4-Substituted Phenyl) Amino) Benzaldehyde". W 2016 7th International Conference on Education, Management, Computer and Medicine (EMCM 2016). Paris, France: Atlantis Press, 2017. http://dx.doi.org/10.2991/emcm-16.2017.109.
Pełny tekst źródłaLiphardt, Martin, Brian Jones, Stephen Ducharme, J. M. Takacs, Lei Zhang i R. V. Athalye. "Photorefractive characterization of polymers". W OSA Annual Meeting. Washington, D.C.: Optica Publishing Group, 1993. http://dx.doi.org/10.1364/oam.1993.mxx.6.
Pełny tekst źródłaChen, Ziqiu, Jianbao Zhao, Brant Billinghurst, Csaba Fábri, Haihua Zhou, Yichi Zhang, Jiarui Ma, Zengkui Liu i Yue Liang. "SYNCHROTRON-BASED HIGH RESOLUTION FAR INFRARED SPECTROSCOPY OF BENZALDEHYDE". W 2020 International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2020. http://dx.doi.org/10.15278/isms.2020.tg03.
Pełny tekst źródłaKim, Jong H., i Kathleen L. Chan. "Benzaldehyde Use to Protect Seeds from Foodborne Fungal Pathogens". W Foods 2022. Basel Switzerland: MDPI, 2022. http://dx.doi.org/10.3390/foods2022-12926.
Pełny tekst źródłaDucharme, Stephen, Brian Jones, Martin Liphardt, Richard Ervin, James M. Takacs, Lei Zhang i Rajan Athalye. "Photorefractive Properties of Bisphenol-A-4,4'-Nitroaminostilbene Mixed with Diethylaminobenzaldehyde-Diphenyl Hydrazone". W Photorefractive Materials, Effects, and Devices II. Washington, D.C.: Optica Publishing Group, 1993. http://dx.doi.org/10.1364/pmed.1993.tha.1.
Pełny tekst źródłaSprau, Christian, i Alexander Colsmann. "The role of benzaldehyde additives in organic bulk-heterojunction solar cells". W Organic, Hybrid, and Perovskite Photovoltaics XXI, redaktorzy Kwanghee Lee, Zakya H. Kafafi, Paul A. Lane, Harald W. Ade i Yueh-Lin (Lynn) Loo. SPIE, 2020. http://dx.doi.org/10.1117/12.2569105.
Pełny tekst źródłaRaporty organizacyjne na temat "Benzaldehyde"
Kallupalayam Ramasamy, Karthikeyan, i Mond Guo. Ethanol to Para-xylene via Methyl Benzaldehyde. Office of Scientific and Technical Information (OSTI), maj 2022. http://dx.doi.org/10.2172/1985305.
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