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Статті в журналах з теми "Natural Products - Carbocyclic compounds"
Banwell, MG. "New Methods for the Synthesis of Troponoid Compounds." Australian Journal of Chemistry 44, no. 1 (1991): 1. http://dx.doi.org/10.1071/ch9910001.
Повний текст джерелаSchmiedel, Volker Martin, and Hans-Ulrich Reissig. "Alkoxyallenes as Starting Materials for the Syntheses of Natural Products." Current Organic Chemistry 23, no. 27 (January 15, 2020): 2976–3003. http://dx.doi.org/10.2174/1385272824666191218115731.
Повний текст джерелаMandal, Sumana, Raju D. Chaudhari, and Goutam Biswas. "Advances in mercury(II)-salt-mediated cyclization reactions of unsaturated bonds." Beilstein Journal of Organic Chemistry 17 (September 9, 2021): 2348–76. http://dx.doi.org/10.3762/bjoc.17.153.
Повний текст джерелаYan, Ning, Yongmei Du, Xinmin Liu, Hongbo Zhang, Yanhua Liu, and Zhongfeng Zhang. "A Review on Bioactivities of Tobacco Cembranoid Diterpenes." Biomolecules 9, no. 1 (January 16, 2019): 30. http://dx.doi.org/10.3390/biom9010030.
Повний текст джерелаMhaske, Santosh, and Ranjeet Dhokale. "Transition-Metal-Catalyzed Reactions Involving Arynes." Synthesis 50, no. 01 (November 22, 2017): 1–16. http://dx.doi.org/10.1055/s-0036-1589517.
Повний текст джерелаChen, Xuefei, Min Xu, Jin Lü, Jianguo Xu, Yemin Wang, Shuangjun Lin, Zixin Deng, and Meifeng Tao. "Biosynthesis of Tropolones inStreptomycesspp.: Interweaving Biosynthesis and Degradation of Phenylacetic Acid and Hydroxylations on the Tropone Ring." Applied and Environmental Microbiology 84, no. 12 (April 13, 2018): e00349-18. http://dx.doi.org/10.1128/aem.00349-18.
Повний текст джерелаOkumura, Mikiko, and David Sarlah. "Arenophile-Mediated Photochemical Dearomatization of Nonactivated Arenes." CHIMIA International Journal for Chemistry 74, no. 7 (August 12, 2020): 577–83. http://dx.doi.org/10.2533/chimia.2020.577.
Повний текст джерелаSmyrniotopoulos, Vangelis, Anna Cláudia de Andrade Tomaz, Maria de Fátima Vanderlei de Souza, Emídio Vasconcelos Leitão da Cunha, Robert Kiss, Véronique Mathieu, Efstathia Ioannou, and Vassilios Roussis. "Halogenated Diterpenes with In Vitro Antitumor Activity from the Red Alga Sphaerococcus coronopifolius." Marine Drugs 18, no. 1 (December 29, 2019): 29. http://dx.doi.org/10.3390/md18010029.
Повний текст джерелаTammam, Mohamed A., Lucie Rárová, Marie Kvasnicová, Gabriel Gonzalez, Ahmed M. Emam, Aldoushy Mahdy, Miroslav Strnad, Efstathia Ioannou, and Vassilios Roussis. "Bioactive Steroids from the Red Sea Soft Coral Sinularia polydactyla." Marine Drugs 18, no. 12 (December 10, 2020): 632. http://dx.doi.org/10.3390/md18120632.
Повний текст джерелаYang, Ji-Min, Yu-Kun Lin, Tao Sheng, Liang Hu, Xin-Pei Cai, and Jin-Quan Yu. "Regio-controllable [2+2] benzannulation with two adjacent C(sp 3 )–H bonds." Science 380, no. 6645 (May 12, 2023): 639–44. http://dx.doi.org/10.1126/science.adg5282.
Повний текст джерелаДисертації з теми "Natural Products - Carbocyclic compounds"
Wong, Wan Yee. "Solvothermal crystallization of organic compounds and natural products /." View abstract or full-text, 2006. http://library.ust.hk/cgi/db/thesis.pl?CHEM%202006%20WONG.
Повний текст джерелаCowe, H. J. de L. "Molecular studies of natural products and related compounds." Thesis, Robert Gordon University, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.370758.
Повний текст джерелаAtkinson, A. M. "Structures of some natural products and metallo-organic compounds." Thesis, Imperial College London, 1988. http://hdl.handle.net/10044/1/46946.
Повний текст джерелаHussain, Amjad. "The synthesis of heterocyclic compounds related to natural products." Thesis, Swansea University, 2001. https://cronfa.swan.ac.uk/Record/cronfa43039.
Повний текст джерелаDengada, Amrapali Harishkumar. "Isolation and Structural Elucidation of Compounds from Natural Products." Thesis, Virginia Tech, 2014. http://hdl.handle.net/10919/64303.
Повний текст джерелаMaster of Science
Fabiano, E. "Synthesis and reactions of amino compounds relating to natural products." Thesis, University of Newcastle Upon Tyne, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.373890.
Повний текст джерелаReddy, P. S. "Synthesis of some biologically active compounds and some natural products." Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 1986. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/3261.
Повний текст джерелаHeltzel, Carl E. "Structural and synthetic studies of bioactive natural products." Diss., Virginia Tech, 1993. http://hdl.handle.net/10919/40067.
Повний текст джерелаPh. D.
Marucci, C. "NATURAL PRODUCTS AS BUILDING BLOCKS AND LEAD COMPOUNDS FOR API PRODUCTION." Doctoral thesis, Università degli Studi di Milano, 2017. http://hdl.handle.net/2434/480029.
Повний текст джерелаSun, Lin. "Application of New Technologies for the Rapid Identification of Compounds from Natural Sources." Thesis, University of Canterbury. Chemistry, 2009. http://hdl.handle.net/10092/4188.
Повний текст джерелаКниги з теми "Natural Products - Carbocyclic compounds"
Mahendra, Rai, and Carpinella Maria Cecilia, eds. Naturally occurring bioactive compounds. Amsterdam: Elsevier, 2006.
Знайти повний текст джерелаBioactive compounds from natural sources: Natural products as lead compounds in drug discovery. 2nd ed. Boca Raton: CRC Press, 2011.
Знайти повний текст джерела1944-, Mulzer J., ed. Natural product synthesis. Berlin: Springer-Verlag, 2005.
Знайти повний текст джерелаShahidi, Fereidoon, and Chi-Tang Ho, eds. Phenolic Compounds in Foods and Natural Health Products. Washington, DC: American Chemical Society, 2005. http://dx.doi.org/10.1021/bk-2005-0909.
Повний текст джерела1951-, Shahidi Fereidoon, Ho Chi-Tang 1944-, and American Chemical Society. Division of Agricultural and Food Chemistry, eds. Phenolic compounds in foods and natural health products. Washington, DC: American Chemical Society, 2005.
Знайти повний текст джерелаPavel, Kočovský, Tureček František, and Hájíček Josef, eds. Synthesis of natural products: Problems of stereoselectivity. Boca Raton, Fla: CRC Press, 1986.
Знайти повний текст джерелаNag, Ahindra. Greener Synthesis of Organic Compounds, Drugs and Natural Products. Boca Raton: CRC Press, 2022. http://dx.doi.org/10.1201/9781003089162.
Повний текст джерелаNatural products and their active compounds on disease prevention. Hauppauge, N.Y: Nova Science Publishers, 2011.
Знайти повний текст джерелаFrom biosynthesis to total synthesis: Strategies and tactics for natural products. Hoboken, New Jersey: John Wiley & Sons, Inc., 2016.
Знайти повний текст джерелаFormulating, packaging, and marketing of natural cosmetic products. Hoboken, N.J: Wiley, 2011.
Знайти повний текст джерелаЧастини книг з теми "Natural Products - Carbocyclic compounds"
Lattanzio, Vincenzo. "Phenolic Compounds: Introduction." In Natural Products, 1543–80. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-22144-6_57.
Повний текст джерелаSadeghi-aliabadi, Hojjat, and Afsaneh Yegdaneh. "Taxol and Related Compounds." In Natural Products, 3159–71. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-22144-6_143.
Повний текст джерелаIgnat, Ioana, Irina Volf, and Valentin I. Popa. "Analytical Methods of Phenolic Compounds." In Natural Products, 2061–92. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-22144-6_56.
Повний текст джерелаLi, Wende, and Trust Beta. "Food Sources of Phenolics Compounds." In Natural Products, 2527–58. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-22144-6_68.
Повний текст джерелаPereira, David M., Patrícia Valentão, Mariana Sottomayor, Federico Ferreres, and Paula B. Andrade. "Phenolic Compounds in Catharanthus roseus." In Natural Products, 2093–106. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-22144-6_96.
Повний текст джерелаRoutray, Winny, and Valérie Orsat. "Preparative Extraction and Separation of Phenolic Compounds." In Natural Products, 2013–45. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-22144-6_55.
Повний текст джерелаSirikantaramas, Supaart, Mami Yamazaki, and Kazuki Saito. "How Plants Avoid the Toxicity of Self-Produced Defense Bioactive Compounds." In Natural Products, 67–82. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118794623.ch4.
Повний текст джерелаDinan, Laurence. "Dereplication and Partial Identification of Compounds." In Natural Products Isolation, 297–321. Totowa, NJ: Humana Press, 2006. http://dx.doi.org/10.1385/1-59259-955-9:297.
Повний текст джерелаGill, M. "Aromatic Compounds." In The Chemistry of Natural Products, 60–105. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-2144-6_2.
Повний текст джерелаKelly, D. R. "Aliphatic compounds." In The Chemistry of Natural Products, 382–441. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-2144-6_9.
Повний текст джерелаТези доповідей конференцій з теми "Natural Products - Carbocyclic compounds"
Sahidin, I., Syefira Salsabila, W. Wahyuni, M. Hajrul Malaka, Imran, and Marianti A. Manggau. "Antibacterial Activity of Methanol Extracts and Compounds of Wualae (Etlingera elatior) Fruits from Southeast Sulawesi-Indonesia." In Bromo Conference, Symposium on Natural Products and Biodiversity. SCITEPRESS - Science and Technology Publications, 2018. http://dx.doi.org/10.5220/0008358901510154.
Повний текст джерелаShin, Moonshik, Sungyoung Yoo, Suhyun Ha, Kyungrin Noh, and Doheon Lee. "Identifying Potential Bioactive Compounds of Natural Products by Combining ADMET Prediction Methods." In CIKM'15: 24th ACM International Conference on Information and Knowledge Management. New York, NY, USA: ACM, 2015. http://dx.doi.org/10.1145/2811163.2811168.
Повний текст джерелаvan Beelen, ESE, and J. Runco. "Purification & isolation of compounds from natural products using an SFE-SFC workflow." In 67th International Congress and Annual Meeting of the Society for Medicinal Plant and Natural Product Research (GA) in cooperation with the French Society of Pharmacognosy AFERP. © Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-3399689.
Повний текст джерелаFerreira Queiroz, E., R. Huber, L. Marcourt, A. Luscher, A. Koval, N. Hanna, J. Nitschke, et al. "Short Lecture “Enzymatically engineered natural products as a source of invaluable bioactive compounds”." In GA – 70th Annual Meeting 2022. Georg Thieme Verlag KG, 2022. http://dx.doi.org/10.1055/s-0042-1758937.
Повний текст джерелаAzkia, Adinda, Sumi Hudiyono, and Sri Handayani. "Study of Enzymatic Synthesis of Glycol – Castor Oil Fatty Acid and Glycol – Palmitic Acid Esters as Emulsifier and Antimicrobial Compounds Using Candida rugosa Lipase EC. 3.1.1.3." In Bromo Conference, Symposium on Natural Products and Biodiversity. SCITEPRESS - Science and Technology Publications, 2018. http://dx.doi.org/10.5220/0008356800050011.
Повний текст джерелаBlagojević, Julijana, Olga Govedarica, Kojić Predrag, Oskar Bera, Mirjana Jovičić, Sonja Stojanov, Jelena Pavličević, and Dragan Govedarica. "INVESTIGATION OF HEMPSEED PROCESS OIL AS THE ALTERNATIVE IN NATURAL RUBBER COMPOUNDING PROCESS." In 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac, 2021. http://dx.doi.org/10.46793/iccbi21.121b.
Повний текст джерелаWickramanayake, Kokila Kumudu, Talaat Abdel-Fattah Ahmed, and Mohammed Hussain S. A. Al safran. "Effect of Plant Growth Regulators on Callus Induction from Leaf and Petiole explants of Hummeid (Rumex Vesicarius)." In Qatar University Annual Research Forum & Exhibition. Qatar University Press, 2021. http://dx.doi.org/10.29117/quarfe.2021.0059.
Повний текст джерелаBrito, Jordana T., Lucas H. Martorano, Ana Carolina F. de Albuquerque, Carlos Magno Rocha Ribeiro, Rodolfo Goetze Fiorot, José Walkimar de Mesquita Carneiro, Alessandra L. Valverde, and Fernando Martins dos Santos Junior. "ESPECTROSCOPIA COMPUTACIONAL APLICADA AO REASSINALAMENTO ESTRUTURAL DE MOLÉCULAS QUIRAIS: HELIANNUOL L." In VIII Simpósio de Estrutura Eletrônica e Dinâmica Molecular. Universidade de Brasília, 2020. http://dx.doi.org/10.21826/viiiseedmol202025.
Повний текст джерелаAlbuquerque, Ana Carolina Ferreira de, José Walkimar de Mesquita Carneiro, and Fernando Martins dos Santos Junior. "Estudo do tautomerismo ceto-enólico da 7-epi-clusianona através de cálculos teóricos de deslocamentos químicos de RMN." In VIII Simpósio de Estrutura Eletrônica e Dinâmica Molecular. Universidade de Brasília, 2020. http://dx.doi.org/10.21826/viiiseedmol202063.
Повний текст джерелаAlexander, Elinor. "Natural hydrogen exploration in South Australia." In PESA Symposium Qld 2022. PESA, 2022. http://dx.doi.org/10.36404/putz2691.
Повний текст джерелаЗвіти організацій з теми "Natural Products - Carbocyclic compounds"
Phillips, Donald A., Yitzhak Spiegel, and Howard Ferris. Optimizing nematode management by defining natural chemical bases of behavior. United States Department of Agriculture, November 2006. http://dx.doi.org/10.32747/2006.7587234.bard.
Повний текст джерелаJander, Georg, and Daniel Chamovitz. Investigation of growth regulation by maize benzoxazinoid breakdown products. United States Department of Agriculture, January 2015. http://dx.doi.org/10.32747/2015.7600031.bard.
Повний текст джерелаNaim, Michael, Andrew Spielman, Shlomo Nir, and Ann Noble. Bitter Taste Transduction: Cellular Pathways, Inhibition and Implications for Human Acceptance of Agricultural Food Products. United States Department of Agriculture, February 2000. http://dx.doi.org/10.32747/2000.7695839.bard.
Повний текст джерелаPaterek, J. Robert. L51963 Environmental Benign Mitigation of Microbiologically Influenced Corrosion (MIC). Chantilly, Virginia: Pipeline Research Council International, Inc. (PRCI), September 2002. http://dx.doi.org/10.55274/r0011299.
Повний текст джерелаAnnunziato, Dominick. HPLC Sample Prep and Extraction SOP v1.3 for Fungi. MagicMyco, August 2023. http://dx.doi.org/10.61073/sopv1.3.08.11.2023.
Повний текст джерелаPhillips, Donald, and Yoram Kapulnik. Using Flavonoids to Control in vitro Development of Vesicular Arbuscular Mycorrhizal Fungi. United States Department of Agriculture, January 1995. http://dx.doi.org/10.32747/1995.7613012.bard.
Повний текст джерелаBrydie, Dr James, Dr Alireza Jafari, and Stephanie Trottier. PR-487-143727-R01 Modelling and Simulation of Subsurface Fluid Migration from Small Pipeline Leaks. Chantilly, Virginia: Pipeline Research Council International, Inc. (PRCI), May 2017. http://dx.doi.org/10.55274/r0011025.
Повний текст джерелаBorch, Thomas, Yitzhak Hadar, and Tamara Polubesova. Environmental fate of antiepileptic drugs and their metabolites: Biodegradation, complexation, and photodegradation. United States Department of Agriculture, January 2012. http://dx.doi.org/10.32747/2012.7597927.bard.
Повний текст джерелаHefetz, Abraham, and Justin O. Schmidt. Use of Bee-Borne Attractants for Pollination of Nonrewarding Flowers: Model System of Male-Sterile Tomato Flowers. United States Department of Agriculture, October 2003. http://dx.doi.org/10.32747/2003.7586462.bard.
Повний текст джерела