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Статті в журналах з теми "030502 Natural Products Chemistry"
Nogueira, Cláudio R., and Lucia M. X. Lopes. "Antiplasmodial Natural Products." Molecules 16, no. 3 (March 4, 2011): 2146–90. http://dx.doi.org/10.3390/molecules16032146.
Повний текст джерелаHill, Robert A. "Marine natural products." Annual Reports Section "B" (Organic Chemistry) 102 (2006): 123. http://dx.doi.org/10.1039/b515100g.
Повний текст джерелаHadi, A. Hamid A., Mehmet Emin Duru, and Ana B. Martin-Diana. "Bioactive Natural Products." Journal of Chemistry 2013 (2013): 1. http://dx.doi.org/10.1155/2013/208507.
Повний текст джерелаHill, Robert A. "Marine natural products." Annual Reports Section "B" (Organic Chemistry) 105 (2009): 150. http://dx.doi.org/10.1039/b822053k.
Повний текст джерелаHill, Robert A. "Marine natural products." Annual Reports Section "B" (Organic Chemistry) 109 (2013): 146. http://dx.doi.org/10.1039/c3oc90008h.
Повний текст джерелаHill, Robert A. "Marine natural products." Annual Reports Section "B" (Organic Chemistry) 107 (2011): 138. http://dx.doi.org/10.1039/c1oc90008k.
Повний текст джерелаHill, Robert A. "Marine natural products." Annual Reports Section "B" (Organic Chemistry) 103 (2007): 125. http://dx.doi.org/10.1039/b614408j.
Повний текст джерелаHill, Robert A. "Marine natural products." Annual Reports Section "B" (Organic Chemistry) 106 (2010): 156. http://dx.doi.org/10.1039/b927083n.
Повний текст джерелаHill, Robert A. "Marine natural products." Annual Reports Section "B" (Organic Chemistry) 104 (2008): 127. http://dx.doi.org/10.1039/b716596j.
Повний текст джерелаKingston, David G. I. "A Natural Love of Natural Products." Journal of Organic Chemistry 73, no. 11 (June 2008): 3975–84. http://dx.doi.org/10.1021/jo800239a.
Повний текст джерелаДисертації з теми "030502 Natural Products Chemistry"
Handley, Paul Newton. "The chemistry of some Australian natural products /." [St. Lucia, Qld.], 2002. http://www.library.uq.edu.au/pdfserve.php?image=thesisabs/absthe16940.pdf.
Повний текст джерелаHeaviside, Elizabeth Anne. "Analogues of antibacterial natural products." Thesis, University of Oxford, 2012. http://ora.ox.ac.uk/objects/uuid:6b5bd771-515b-49d0-8ec9-cee115d3aebf.
Повний текст джерелаAnderson, Margaret Marie. "Cytotoxic and antimalarial natural products." Thesis, University College London (University of London), 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.320404.
Повний текст джерелаvan, der Sar Sonia. "Studies in the chemistry of fungal natural products." Thesis, University of Canterbury. Chemistry, 2006. http://hdl.handle.net/10092/1333.
Повний текст джерелаHickford, Sarah Jane Herbison. "Studies in the Chemistry of Marine Natural Products." Thesis, University of Canterbury. Chemistry, 2007. http://hdl.handle.net/10092/1429.
Повний текст джерела施麗琼 and Lai-king Sy. "Structure elucidation and oxidation chemistry of natural products." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1998. http://hub.hku.hk/bib/B3123768X.
Повний текст джерелаJabbar, Abdul. "The chemistry of natural products of the Rutaceae." Thesis, University of Aberdeen, 1987. http://digitool.abdn.ac.uk/R?func=search-advanced-go&find_code1=WSN&request1=AAIU498401.
Повний текст джерелаSy, Lai-king. "Structure elucidation and oxidation chemistry of natural products /." Hong Kong : University of Hong Kong, 1998. http://sunzi.lib.hku.hk/hkuto/record.jsp?B19737300.
Повний текст джерелаBlasiak, Leah Cameron. "Crystallographic studies on enzymatic halogenation of natural products." Thesis, Massachusetts Institute of Technology, 2008. http://hdl.handle.net/1721.1/42914.
Повний текст джерелаThis electronic version was submitted by the student author. The certified thesis is available in the Institute Archives and Special Collections.
Vita.
Includes bibliographical references.
Halogenated natural products are common and serve roles as hormones, pesticides, antibiotics, and anti-tumor agents. The incorporation of a halogen atom into an organic scaffold can tune the molecule's potency and selectivity, making halogenation an important tailoring reaction. To understand the mechanisms of enzymatic halogenation of natural products, X-ray crystallography was used to solve structures of enzymes from two classes of halogenases, the flavin-dependent halogenases and the non-heme iron dependent halogenases. Structures of the flavin-dependent tryptophan 7-halogenase RebH from Lechevalieria aerocolonigenes, involved in rebeccamycin biosynthesis, were solved by molecular replacement. These structures show distant flavin and L-Trp binding sites and identify the conserved residue Lys79 as a likely candidate for covalent modification to produce an enzyme-bound lysine chloramine intermediate. A lysine chloramine at this position would direct the chlorination reaction to the correct site on the substrate, which could account for the halogenase's observed regioselectivity. Crystal structures of the non-heme iron-dependent threonine 4-halogenase SyrB2 from Pseudomonas syringae, involved in syringomycin biosynthesis, were solved using selenomethionine labeling and single wavelength anomalous dispersion (SAD) techniques. These structures show an overall cupin or [beta]-sandwich fold and a novel iron binding motif containing a naturally occurring iron-chloride bond. The carboxylate ligand typically found in non-heme iron dependent hydroxylases is replaced by an alanine residue in the halogenases, opening a coordination site for the halide and suggesting a mechanism by which these enzymes accomplish halogenation instead of hydroxylation.
(cont)The final chapter of this thesis reviews the known classes of halogenating enzymes and examines questions of halide binding and selectivity from the perspective of protein structure.
by Leah Cameron Blasiak.
Ph.D.
Mahaney, Paige E. (Paige Erin). "Efforts toward the synthesis of taxane natural products." Thesis, Massachusetts Institute of Technology, 1996. http://hdl.handle.net/1721.1/38760.
Повний текст джерелаКниги з теми "030502 Natural Products Chemistry"
Atta-ur-Rahman and Philip William Le Quesne, eds. Natural Products Chemistry III. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-74017-6.
Повний текст джерелаAhluwalia, V. K., Lalita S. Kumar, and Sanjiv Kumar. Chemistry of Natural Products. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-86698-3.
Повний текст джерела1918-, Barton Derek Sir, Nakanishi Kōji 1925-, and Meth-Cohn Otto, eds. Comprehensive natural products chemistry. Amsterdam: Elsevier, 1999.
Знайти повний текст джерелаRahman, Atta-ur. Bioactive natural products. Amsterdam: Elsevier, 2000.
Знайти повний текст джерелаP, Cannell Richard J., ed. Natural products isolation. Totowa, N.J: Humana Press, 1998.
Знайти повний текст джерелаIntroduction to natural products chemistry. Boca Raton, Fla: Taylor & Francis, 2011.
Знайти повний текст джерелаRaymond, Cooper, and George Nicola. Natural Products Chemistry. Taylor & Francis Group, 2015.
Знайти повний текст джерелаNatural Products Chemistry. Taylor & Francis Group, 2020.
Знайти повний текст джерелаAtta-ur-Rahman. Studies in Natural Products Chemistry: Bioactive Natural Products. Elsevier, 2016.
Знайти повний текст джерелаAtta-ur-Rahman. Studies in Natural Products Chemistry: Bioactive Natural Products. Elsevier, 2012.
Знайти повний текст джерелаЧастини книг з теми "030502 Natural Products Chemistry"
Appendino, Giovanni, and Orazio Taglialatela-Scafati. "Cannabinoids: Chemistry and Medicine." In Natural Products, 3415–35. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-22144-6_147.
Повний текст джерелаPaquette, Leo A., and Annette M. Doherty. "Natural Products Chemistry." In Reactivity and Structure Concepts in Organic Chemistry, 107–11. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-72598-2_6.
Повний текст джерелаChoudhary, M. Iqbal, Sammer Yousuf, and Atta-ur-Rahman. "Withanolides: Chemistry and Antitumor Activity." In Natural Products, 3465–95. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-22144-6_150.
Повний текст джерелаChakraborty, Dipjyoti, and Amita Pal. "Quassinoids: Chemistry and Novel Detection Techniques." In Natural Products, 3345–66. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-22144-6_144.
Повний текст джерелаKacprzak, Karol Michał. "Chemistry and Biology of Cinchona Alkaloids." In Natural Products, 605–41. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-22144-6_22.
Повний текст джерелаDembitsky, Valery M., Alexander O. Terent’ev, and Dmitri O. Levitsky. "Aziridine Alkaloids: Origin, Chemistry and Activity." In Natural Products, 977–1006. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-22144-6_93.
Повний текст джерелаSingh, Rajeev, Hema Joshi, and Anamika Singh. "Bryophytes: Natural Biomonitors." In Natural Products Chemistry, 139–53. Names: Volova, Tatiana G., editor. | Mahapatra, Debarshi Kar, editor. | Khanna, Sonia, editor. | Haghi, A. K., editor. Description: Includes bibliographical references and index.: Apple Academic Press, 2020. http://dx.doi.org/10.1201/9781003000693-7.
Повний текст джерелаBrahmkshatriya, Priyanka P., and Pathik S. Brahmkshatriya. "Terpenes: Chemistry, Biological Role, and Therapeutic Applications." In Natural Products, 2665–91. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-22144-6_120.
Повний текст джерелаSchmalz, Hans-Günther, Battsengel Gotov, and Andreas Böttcher. "Natural Products Synthesis." In Topics in Organometallic Chemistry, 157–79. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/b94494.
Повний текст джерелаShishatskaya, E. I., S. V. Prudnikova, A. A. Shumiliva, and T. G. Volova. "Bacterial Nanocellulose: Synthesis, Properties, Hybrids with Nano-Silver for Tissue Engineering." In Natural Products Chemistry, 1–39. Names: Volova, Tatiana G., editor. | Mahapatra, Debarshi Kar, editor. | Khanna, Sonia, editor. | Haghi, A. K., editor. Description: Includes bibliographical references and index.: Apple Academic Press, 2020. http://dx.doi.org/10.1201/9781003000693-1.
Повний текст джерелаТези доповідей конференцій з теми "030502 Natural Products Chemistry"
Pachlatko, J. "Natural Products in Crop Protection." In The 2nd International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 1998. http://dx.doi.org/10.3390/ecsoc-2-01701.
Повний текст джерелаPezzani, Raffaele. "Plant natural products with anti-thyroid cancer activity." In 6th International Electronic Conference on Medicinal Chemistry. Basel, Switzerland: MDPI, 2020. http://dx.doi.org/10.3390/ecmc2020-07252.
Повний текст джерелаAchmad, Sjamsul Arifin, Euis Holisotan Hakim, Lia Dewi Juliawaty, Lukman Makmur, Yana Maolana Syah, and Didin Mujahidin. "Organic chemistry of natural products in Indonesia: Opportunity, achievement and challenges." In THE 5TH INTERNATIONAL CONFERENCE ON MATHEMATICS AND NATURAL SCIENCES. AIP Publishing LLC, 2015. http://dx.doi.org/10.1063/1.4930622.
Повний текст джерелаFonseca, André, Maria Matos, Saleta Vazquez-Rodriguez, Dolores Viña, Santiago Vilar, Fernanda Borges, Lourdes Santana, and Eugenio Uriarte. "Structural Modifications on Natural-based Products: Synthetic Strategies and Biological Applications." In The 18th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-b023.
Повний текст джерелаCouture, Axel, Marc Lamblin, Anne Moreau, Eric Deniau, Stéphane Lebrun, and Pierre Grandclaudon. "New Developments of the Parham Cyclization Process. Applications in Natural Products Synthesis." In The 9th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2005. http://dx.doi.org/10.3390/ecsoc-9-01479.
Повний текст джерелаLoiseau, Philippe, Kaluvu Balaraman, Nalia Mekarnia, Gillian Barratt, Sébastien Pomel, Sandrine Cojean, Venkitasamy Kesavan, Atipetha Jayakrishnan, and Bruno Fidadère. "Drug Targeting of Natural Products: the Example of Antileishmanial Quinolines." In 3rd International Electronic Conference on Medicinal Chemistry. Basel, Switzerland: MDPI, 2017. http://dx.doi.org/10.3390/ecmc-3-04649.
Повний текст джерелаThiericke, Ralf, Yuan-Qing Tang, Isabel Sattler, Susanne Grabley, and Xiao-Zhang Feng. "Parallel Chromatography in Natural Products Chemistry: Isolation of New Secondary Metabolites from Streptomyces sp." In The 4th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01914.
Повний текст джерелаLiebler, Eduard K., Katrin B. Lorenz, Björn Dietrich, Katja Bensmann, Britta Eickmann, and Ulf Diederichsen. "DNA binding of peptides derived from natural products or proteins and bending of DNA double strands." In XIIIth Symposium on Chemistry of Nucleic Acid Components. Prague: Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2005. http://dx.doi.org/10.1135/css200507065.
Повний текст джерелаМелентьев, Гелий. "Manufacturing finished rare-metal products from natural raw minerals and artificial formations using innovation pyrochemical methods instead of conventional techniques." In Mineralogical and technological appraisal of new types of mineral products. Petrozavodsk: Karelian Research Center of RAS, 2019. http://dx.doi.org/10.17076/tm13_5.
Повний текст джерелаFatimi, Ahmed. "Patent analysis of a medicinal plant as a source of natural products and drugs: <em>Rosmarinus officinalis</em> (Rosemary)." In 7th International Electronic Conference on Medicinal Chemistry. Basel, Switzerland: MDPI, 2021. http://dx.doi.org/10.3390/ecmc2021-11346.
Повний текст джерела