Gotowe bibliografie tematyczne / Stereochemistry

Gotowa bibliografia na temat „Stereochemistry”

Autor: Grafiati
Data publikacji: 4 czerwca 2021
Data aktualizacji: 1 czerwca 2024

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Artykuły w czasopismach na temat "Stereochemistry"

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Wood, E. "Stereochemistry". Biochemistry and Molecular Biology Education 29, nr 5 (wrzesień 2001): 216. http://dx.doi.org/10.1016/s1470-8175(01)00068-6.

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Agami, Claude, i Toufic Rizk. "Stereochemistry-60". Tetrahedron 41, nr 3 (styczeń 1985): 537–40. http://dx.doi.org/10.1016/s0040-4020(01)96496-8.

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Walba, David M. "Topological stereochemistry". Tetrahedron 41, nr 16 (styczeń 1985): 3161–212. http://dx.doi.org/10.1016/s0040-4020(01)96671-2.

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Shallenberger, Robert S., i Wanda J. Wienen. "Carbohydrate stereochemistry". Journal of Chemical Education 66, nr 1 (styczeń 1989): 67. http://dx.doi.org/10.1021/ed066p67.

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Gibb, Bruce C. "Supramolecular Stereochemistry". Journal of Supramolecular Chemistry 2, nr 1-3 (styczeń 2002): 123–31. http://dx.doi.org/10.1016/s1472-7862(02)00088-6.

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Kellogg, Richard M. "Practical Stereochemistry". Accounts of Chemical Research 50, nr 4 (marzec 2017): 905–14. http://dx.doi.org/10.1021/acs.accounts.6b00630.

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"Stereochemistry". Carbohydrate Polymers 50, nr 1 (1.10.2002): 96. http://dx.doi.org/10.1016/s0144-8617(01)00368-x.

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Kusumaningdyah, Rooserina, Iztok Devetak, Yudhi Utomo, Effendy Effendy, Daratu Putri i Habiddin Habiddin. "Teaching Stereochemistry with Multimedia and Hands-On Models: The Relationship between Students’ Scientific Reasoning Skills and The Effectiveness of Model Type". Center for Educational Policy Studies Journal, 31.05.2023. http://dx.doi.org/10.26529/cepsj.1547.

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This paper presents an analysis of the use of multimedia and hands-on models on university students’ understanding of stereochemistry. The relationship between students’ scientific reasoning skills and their understanding of stereochemistry was also determined. Two groups of second-year chemistry students from the State University of Malang taking organic chemistry for the 2020/21 academic year participated in this study. One group of students experienced stereochemistry teaching using multimedia models and the other hands-on models as the learning medium. Lawson’s Classroom Test of Scientific Reasoning and Short-Answer Stereochemistry Test were applied. The former was deployed to measure students’ scientific reasoning skills, while the latter was used to test their understanding of stereochemistry. The results revealed that the students’ scientific reasoning skills were significantly below the expected standard, falling in the low category. Students with high scientific reasoning skills exhibited a better understanding of stereochemistry than those with low levels. Both multimedia and hands-on models revealed an equal contribution towards students’ understanding of stereochemistry. Also, it suggests that multimedia models tend to favour students with high scientific reasoning skills, while hands-on models favour those with low skills.
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Ippoliti, Francesca M., Melinda M. Nguyen, Amber J. Reilly i Neil K. Garg. "Gaming stereochemistry". Nature Reviews Chemistry, 12.05.2022. http://dx.doi.org/10.1038/s41570-022-00395-5.

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"Stereochemistry abstracts". Tetrahedron: Asymmetry 14, nr 3 (luty 2003): A49—A72. http://dx.doi.org/10.1016/s0957-4166(03)00062-4.

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Rozprawy doktorskie na temat "Stereochemistry"

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Barr, Stephen Alexander. "Quinoline alkaloids : synthesis and stereochemistry". Thesis, Queen's University Belfast, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.333796.

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Kreisberg, Jennifer Diane. "Studies directed towards the total synthesis of the natural product diazonamide A". Access restricted to users with UT Austin EID Full text (PDF) from UMI/Dissertation Abstracts International, 2001. http://wwwlib.umi.com/cr/utexas/fullcit?p3037513.

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Holzbaur, Ines Elizabeth. "Control of stereochemistry in erythromycin biosynthesis". Thesis, University of Cambridge, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.624787.

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Silvary, Sunil Raj. "StereoElectronic Controls in the Preparation of 1-Benzyl-l, 2, 4, 5-Tetrahydro-(3H)-2-Benzazepin-3-ones Via Beckmann Rearrangement". Fogler Library, University of Maine, 2007. http://www.library.umaine.edu/theses/pdf/SilvarySR2007.pdf.

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Bates, Tim Frank. "The Stereochemistry of Silenes and Alpha-Lithio Silanes". Thesis, North Texas State University, 1987. https://digital.library.unt.edu/ark:/67531/metadc332323/.

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When E- or Z-l-methyl-l-phenyl-2-neopentylsilene was generated by the retro-Diels-Alder vacuum-sealed tube thermolysis of its corresponding anthracene adduct, in the presence of various alkoxysilanes, only one diastereomeric adduct was formed in each case, showing that the reactions are stereospecific. An x-ray crystal structure of the methoxytriphenylsilane adduct of the E-silene confirmed its relative configuration as (R,S) or (S,R). This demonstrated that the addition of alkoxysilanes to silenes is stereospecific and syn. The relative configurations of similar alkoxysilane and alkoxystannane adducts to E- and Z-l-methyl-l-phenyl-2-neopentylsilene were assigned based on a combination of xray structures and *3C NMR data. A strong, nonbonded oxygen-metal interaction is apparent in all of those compounds studied. Treatment of the alkoxystannane adducts with alkyl lithium reagents results in tin-lithium exchange in some cases. The results indicate that the resulting
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Pitt, A. R. "Stereochemistry and mechanism of isopenicillin N synthase". Thesis, University of Oxford, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.235052.

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Kennedy, D. A. "Crystallographic studies of relative and absolute stereochemistry". Thesis, Queen's University Belfast, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.373533.

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Okunishi, Tomoya. "Stereochemistry of Lignan Biosynthesis in Thymelaeaceae Plants". Kyoto University, 2003. http://hdl.handle.net/2433/149001.

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Kyoto University (京都大学)
0048
新制・課程博士
博士(農学)
甲第10276号
農博第1348号
新制||農||869(附属図書館)
学位論文||H15||N3797(農学部図書室)
UT51-2003-H697
京都大学大学院農学研究科応用生命科学専攻
(主査)教授 島田 幹夫, 教授 桑原 保正, 教授 坂田 完三
学位規則第4条第1項該当
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Alexander, Andrew James. "The dynamical stereochemistry of photon-initiated bimolecular reactions". Thesis, University of Oxford, 1997. http://ora.ox.ac.uk/objects/uuid:b50aaa50-5605-42e3-aa2a-4f4686df942f.

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The product state specific stereodynamics of the photon–initiated reaction of O(¹D₂) with H₂ has been investigated by polarised Doppler–resolved laser induced fluorescence, under room temperature bulb conditions. Product state resolved differential cross sections, excitation functions and rotational angular momentum alignments are reported for the following product channels, O(¹D₂) + H₂(¹Σ+g ; v = 0) -> OH(X²Pi; v' = 0;N' = 14; f) + H(²S). at a mean collision energy of 12 kJ mol-1. The data are compared with extensive state resolved quasi–classical trajectory (QCT) calculations of the linear and angular momentum distributions and excitation functions conducted on the Schinke–Lester (SL1) and K ab initio ground state (1¹A') potential energy surfaces. Overall, good agreement is obtained between the QCT calculated and experimentally determined stereodynamical features. The results are discussed in light of other recent work on this prototypical insertion reaction, and on the related systems of O(¹D₂) + HD and CH₄.
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Carroll, Jonathan G. "Structure, stereochemistry and reactions of aza-polycyclic metabolites". Thesis, Queen's University Belfast, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.322770.

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Książki na temat "Stereochemistry"

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Morris, David G. Stereochemistry. New York, NY: Wiley-Interscience, 2002.

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Morris, David G. Stereochemistry. Cambridge: Royal Society of Chemistry, 2001.

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Zhu, Hua-Jie. Organic Stereochemistry. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2015. http://dx.doi.org/10.1002/9783527688166.

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Siegel, Jay S., red. Supramolecular Stereochemistry. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-0353-4.

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Siegel, Jay S. Supramolecular Stereochemistry. Dordrecht: Springer Netherlands, 1995.

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Fujita, Shinsaku. Mathematical stereochemistry. Berlin: De Gruyter, 2015.

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NATO Advanced Research Workshop on Supramolecular Stereochemistry (1994 Hveragerði, Iceland). Supramolecular stereochemistry. Dordrecht: Kluwer Academic, 1995.

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Schmiermund, Torsten. Introduction to Stereochemistry. Wiesbaden: Springer Fachmedien Wiesbaden, 2021. http://dx.doi.org/10.1007/978-3-658-32035-5.

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Eliel, Ernest L., Samuel H. Wilen i Norman L. Allinger, red. Topics in Stereochemistry. Hoboken, NJ, USA: John Wiley & Sons, Inc., 1986. http://dx.doi.org/10.1002/9780470147252.

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Eliel, Ernest L., i Samuel H. Wilen, red. Topics in Stereochemistry. Hoboken, NJ, USA: John Wiley & Sons, Inc., 1987. http://dx.doi.org/10.1002/9780470147269.

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Części książek na temat "Stereochemistry"

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Norman, Richard, i James M. Coxon. "Stereochemistry". W Principles of Organic Synthesis, 134–77. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-2166-8_5.

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Gooch, Jan W. "Stereochemistry". W Encyclopedic Dictionary of Polymers, 700. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_11204.

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Bruylants, Gilles. "Stereochemistry". W Encyclopedia of Astrobiology, 2376. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-44185-5_1908.

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Bruylants, Gilles. "Stereochemistry". W Encyclopedia of Astrobiology, 1598. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-11274-4_1908.

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Sarker, Satyajit D., i Lutfun Nahar. "Stereochemistry". W Chemistry for Pharmacy Students, 35–58. West Sussex, England: John Wiley & Sons, Ltd,., 2013. http://dx.doi.org/10.1002/9781118687529.ch3.

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Andraos, John, i Albert S. Matlack. "Stereochemistry". W Introduction to Green Chemistry, 311–38. Wyd. 3. Boca Raton: CRC Press, 2022. http://dx.doi.org/10.1201/9781003033615-10.

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Bruylants, Gilles. "Stereochemistry". W Encyclopedia of Astrobiology, 1. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-27833-4_1908-4.

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Zhao, Wenyi. "Stereochemistry". W Handbook for Chemical Process Research and Development, Second Edition, 557–606. Wyd. 2. Boca Raton: CRC Press, 2023. http://dx.doi.org/10.1201/9781003288411-16.

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Bruylants, Gilles. "Stereochemistry". W Encyclopedia of Astrobiology, 2884. Berlin, Heidelberg: Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65093-6_1908.

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Went, C. "Basic Stereochemistry". W Work Out Organic Chemistry, 18–42. London: Macmillan Education UK, 1988. http://dx.doi.org/10.1007/978-1-349-09726-5_2.

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Streszczenia konferencji na temat "Stereochemistry"

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Linington, Peter F. "The Stereochemistry of Enterprise Objects". W 2010 14th IEEE International Enterprise Distributed Object Computing Conference Workshops (EDOCW). IEEE, 2010. http://dx.doi.org/10.1109/edocw.2010.25.

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Etzlstorfer, Christoph, Heinz Falk, Norbert Müller, Wolfgang Schmitzberger i Ulrike G. Wagner. "Investigations on the stereochemistry of hypericin". W The first European conference on computational chemistry (E.C.C.C.1). AIP, 1995. http://dx.doi.org/10.1063/1.47678.

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Wilson, Mick A., Craig Marshall, Adam Moy i G. S. Kamali Kannangara. "Stereochemistry of carbon nanotubes for electronic applications". W International Symposium on Microelectronics and MEMS, redaktorzy Jung-Chih Chiao, Lorenzo Faraone, H. Barry Harrison i Andrei M. Shkel. SPIE, 2001. http://dx.doi.org/10.1117/12.448964.

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Sekikawa, T., N. Saito, Y. Kurimoto, N. Ishii, T. Mizuno, T. Kanai, J. Itatani, K. Saita i T. Taketsugu. "Direct Confirmation of the Woodward-Hoffmann Rule by Femtosecond Transient Soft X-ray Absorption". W International Conference on Ultrafast Phenomena. Washington, D.C.: Optica Publishing Group, 2022. http://dx.doi.org/10.1364/up.2022.th4a.1.

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The chemical shifts of the carbon K-edge during the ring-opening dynamics of 1,3-cyclohexadiene observed by femtosecond transient soft X-ray absorption confirm that the stereochemistry of the ring-opening reaction follows the Woodward-Hoffmann rule.
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Yang, Wen-Bin, Yu-Feng Gu, Shwu-Huey Wang i Chun-Hung Lin. "STEREOCHEMISTRY IN THE SYNTHESIS AND REACTION OF EXO-GLYCALS". W XXIst International Carbohydrate Symposium 2002. TheScientificWorld Ltd, 2002. http://dx.doi.org/10.1100/tsw.2002.655.

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Grunewald Nichele, Aline, i Fabiane Nunes da Silva. "LEARNING DURING THE PANDEMIC: A PROPOSAL TO STUDY STEREOCHEMISTRY". W 17th International Technology, Education and Development Conference. IATED, 2023. http://dx.doi.org/10.21125/inted.2023.0623.

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Grunewald Nichele, Aline, Kênya Silva dos Santos Moraes i Fabiane Nunes da Silva. "CREATING A PEDAGOGICAL PROPOSAL USING INFOGRAPHICS TO TEACH STEREOCHEMISTRY". W 14th annual International Conference of Education, Research and Innovation. IATED, 2021. http://dx.doi.org/10.21125/iceri.2021.1522.

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Resende*, Gabriela da C., i Elson S. de Alvarenga. "Cycloadducts Synthesis and Relative Stereochemistry Determined by NMR and DFT-GIAO calculations". W 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_20139711943.

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Hood, Patrick J., Alison M. Thomas i Chrysa M. Theodore. "Effects of stereochemistry on the static and dynamic performance of glassy liquid crystals". W International Symposium on Optical Science and Technology, redaktor Iam-Choon Khoo. SPIE, 2000. http://dx.doi.org/10.1117/12.405309.

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Bricogne, Gérard. "Computational aspects of protein crystallography: entropy, likelihood, error-correcting codes, and statistical stereochemistry". W The first European conference on computational chemistry (E.C.C.C.1). AIP, 1995. http://dx.doi.org/10.1063/1.47748.

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