Bibliografie tematiche / Stereochemistry

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Letteratura scientifica selezionata sul tema "Stereochemistry"

Autore: Grafiati
Pubblicato: 4 giugno 2021
Ultima modifica: 25 luglio 2025

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Articoli di riviste sul tema "Stereochemistry"

1

Wood, E. "Stereochemistry." Biochemistry and Molecular Biology Education 29, no. 5 (2001): 216. http://dx.doi.org/10.1016/s1470-8175(01)00068-6.

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Mohd, Sharique Katchhi* Disha Kumareshi Harshitha M. V. Chakure Aditya Abrar Ahmed5. "The Role Of Stereochemistry And Formulation In Pharmacology Of The Drug." International Journal in Pharmaceutical Sciences 2, no. 3 (2024): 790–802. https://doi.org/10.5281/zenodo.10850235.

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Abstract (sommario):
Stereochemistry profoundly influences the pharmacological properties of various drug classes, including antipsychotics, cardiovascular drugs, antibiotics, and antivirals. This review explores the impact of stereochemistry on drug efficacy, safety, and formulation across these therapeutic categories. Enantiomeric differences in drugs such as citalopram and beta-blockers highlight the significance of selecting the more active stereoisomer for improved clinical outcomes. Advanced drug formulations, including extended-release options and novel delivery systems, offer enhanced convenience and effic
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3

Agami, Claude, and Toufic Rizk. "Stereochemistry-60." Tetrahedron 41, no. 3 (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, no. 16 (1985): 3161–212. http://dx.doi.org/10.1016/s0040-4020(01)96671-2.

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5

Shallenberger, Robert S., and Wanda J. Wienen. "Carbohydrate stereochemistry." Journal of Chemical Education 66, no. 1 (1989): 67. http://dx.doi.org/10.1021/ed066p67.

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6

Gibb, Bruce C. "Supramolecular Stereochemistry." Journal of Supramolecular Chemistry 2, no. 1-3 (2002): 123–31. http://dx.doi.org/10.1016/s1472-7862(02)00088-6.

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7

Kellogg, Richard M. "Practical Stereochemistry." Accounts of Chemical Research 50, no. 4 (2017): 905–14. http://dx.doi.org/10.1021/acs.accounts.6b00630.

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8

"Stereochemistry." Carbohydrate Polymers 50, no. 1 (2002): 96. http://dx.doi.org/10.1016/s0144-8617(01)00368-x.

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9

Kusumaningdyah, Rooserina, Iztok Devetak, Yudhi Utomo, Effendy Effendy, Daratu Putri, and 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, May 31, 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
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Ippoliti, Francesca M., Melinda M. Nguyen, Amber J. Reilly, and Neil K. Garg. "Gaming stereochemistry." Nature Reviews Chemistry, May 12, 2022. http://dx.doi.org/10.1038/s41570-022-00395-5.

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Tesi sul tema "Stereochemistry"

1

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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2

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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Abstract (sommario):
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 alkoxystannan
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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)<br>0048<br>新制・課程博士<br>博士(農学)<br>甲第10276号<br>農博第1348号<br>新制||農||869(附属図書館)<br>学位論文||H15||N3797(農学部図書室)<br>UT51-2003-H697<br>京都大学大学院農学研究科応用生命科学専攻<br>(主査)教授 島田 幹夫, 教授 桑原 保正, 教授 坂田 完三<br>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<sup>+</sup><sub>g</sub> ; v = 0) -> OH(X²Pi; v' = 0;N' = 14; f) + H(²S). at a mean collision energy of 12 kJ mol<sup>-1</sup>. The data are compared with extensive state resolved quasi–classical trajectory (
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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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Libri sul tema "Stereochemistry"

1

Royal Society of Chemistry (Great Britain), ed. Stereochemistry. Wiley-Interscience, 2002.

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2

Royal Society of Chemistry (Great Britain), ed. Stereochemistry. Royal Society of Chemistry, 2001.

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3

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

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4

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

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5

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

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6

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

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7

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

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8

Schmiermund, Torsten. Introduction to Stereochemistry. 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, and Norman L. Allinger, eds. Topics in Stereochemistry. John Wiley & Sons, Inc., 1986. http://dx.doi.org/10.1002/9780470147252.

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Eliel, Ernest L., and Samuel H. Wilen, eds. Topics in Stereochemistry. John Wiley & Sons, Inc., 1987. http://dx.doi.org/10.1002/9780470147269.

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Capitoli di libri sul tema "Stereochemistry"

1

Norman, Richard, and James M. Coxon. "Stereochemistry." In Principles of Organic Synthesis. Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-2166-8_5.

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2

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

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

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

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Sarker, Satyajit D., and Lutfun Nahar. "Stereochemistry." In Chemistry for Pharmacy Students. John Wiley & Sons, Ltd,., 2013. http://dx.doi.org/10.1002/9781118687529.ch3.

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

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Zhao, Wenyi. "Stereochemistry." In Handbook for Chemical Process Research and Development, Second Edition, 2nd ed. CRC Press, 2023. http://dx.doi.org/10.1201/9781003288411-16.

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Andraos, John, and Albert S. Matlack. "Stereochemistry." In Introduction to Green Chemistry, 3rd ed. CRC Press, 2022. http://dx.doi.org/10.1201/9781003033615-10.

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

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Tucker, William B. "Stereochemistry." In Organic Chemistry. CRC Press, 2024. http://dx.doi.org/10.1201/9781003479352-6.

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Atti di convegni sul tema "Stereochemistry"

1

Linington, Peter F. "The Stereochemistry of Enterprise Objects." In 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, and Ulrike G. Wagner. "Investigations on the stereochemistry of hypericin." In 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, and G. S. Kamali Kannangara. "Stereochemistry of carbon nanotubes for electronic applications." In International Symposium on Microelectronics and MEMS, edited by Jung-Chih Chiao, Lorenzo Faraone, H. Barry Harrison, and Andrei M. Shkel. SPIE, 2001. http://dx.doi.org/10.1117/12.448964.

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Sekikawa, T., N. Saito, Y. Kurimoto, et al. "Direct Confirmation of the Woodward-Hoffmann Rule by Femtosecond Transient Soft X-ray Absorption." In International Conference on Ultrafast Phenomena. Optica Publishing Group, 2022. http://dx.doi.org/10.1364/up.2022.th4a.1.

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Abstract (sommario):
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, and Chun-Hung Lin. "STEREOCHEMISTRY IN THE SYNTHESIS AND REACTION OF EXO-GLYCALS." In XXIst International Carbohydrate Symposium 2002. TheScientificWorld Ltd, 2002. http://dx.doi.org/10.1100/tsw.2002.655.

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Grunewald Nichele, Aline, and Fabiane Nunes da Silva. "LEARNING DURING THE PANDEMIC: A PROPOSAL TO STUDY STEREOCHEMISTRY." In 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, and Fabiane Nunes da Silva. "CREATING A PEDAGOGICAL PROPOSAL USING INFOGRAPHICS TO TEACH STEREOCHEMISTRY." In 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., and Elson S. de Alvarenga. "Cycloadducts Synthesis and Relative Stereochemistry Determined by NMR and DFT-GIAO calculations." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_20139711943.

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Hood, Patrick J., Alison M. Thomas, and Chrysa M. Theodore. "Effects of stereochemistry on the static and dynamic performance of glassy liquid crystals." In International Symposium on Optical Science and Technology, edited by 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." In 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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Rapporti di organizzazioni sul tema "Stereochemistry"

1

สุวรรณบริรักษ์, คณิต, та สุรัตนา อำนวยผล. การศึกษาทางพฤกษเคมีของต้นข้าวหลาม : รายงานผลการวิจัย. จุฬาลงกรณ์มหาวิทยาลัย, 1996. https://doi.org/10.58837/chula.res.1996.14.

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ได้ทำการสกัดแยกสารจากเปลือกต้นข้าวหลาม Goniothalamus marcanii Craib โดยใช้วิธีทางโครมาโทกราฟีควบคู่ไปกับผลการทดสอบฤทธิ์ทางชีวภาพ ทำให้สามารถแยกสารได้ 4 กลุ่ม โดยการวิเคราะห์ข้อมูลจากสเปกโทรสโกปีเพื่อพิสูจน์สูตรโครงสร้างทางเคมีของสารที่แยกได้ ทำให้ทราบว่าสารทั้ง 4 กลุ่มคือ 1-azaanthraquinones, flavanoids, triterpenoids และ mono-THF annonaceous acetogenins โดยที่สารกลุ่ม 1-azaanthraquinoes ที่แยกได้เป็นสารชนิดใหม่ 1 ชนิด คือ marcanine C ร่วมกับสารที่ทราบสูตรโครงสร้างแล้ว 2 ชนิด คือ marcanine A และ dielsiquinone ส่วนสารกลุ่ม flavanoids ที่แยกได้เป็นสารที่ทราบสูตรโครงสร้างแล้ว 1 ชนิด คือ pinocembr
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