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Artykuły w czasopismach na temat "Sesquiterpenes"
Coca-Ruíz, Víctor, Ivonne Suárez, Josefina Aleu i Isidro G. Collado. "Structures, Occurrences and Biosynthesis of 11,12,13-Tri-nor-Sesquiterpenes, an Intriguing Class of Bioactive Metabolites". Plants 11, nr 6 (14.03.2022): 769. http://dx.doi.org/10.3390/plants11060769.
Pełny tekst źródłaSilva, Waldeyr M. C. da, Jakob L. Andersen, Maristela T. Holanda, Maria Emília M. T. Walter, Marcelo M. Brigido, Peter F. Stadler i Christoph Flamm. "Exploring Plant Sesquiterpene Diversity by Generating Chemical Networks". Processes 7, nr 4 (25.04.2019): 240. http://dx.doi.org/10.3390/pr7040240.
Pełny tekst źródłaWang, Junchi, Qi Zheng, Huaxiang Wang, Leiling Shi, Guoping Wang, Yaqin Zhao, Congzhao Fan i Jianyong Si. "Sesquiterpenes and Sesquiterpene Derivatives from Ferula: Their Chemical Structures, Biosynthetic Pathways, and Biological Properties". Antioxidants 13, nr 1 (19.12.2023): 7. http://dx.doi.org/10.3390/antiox13010007.
Pełny tekst źródłaSaifudin, Azis, Ken Tanaka, Shigetoshi Kadota i Yasuhiro Tezuka. "Chemical Constituents of Blumea balsamifera of Indonesia and Their Protein Tyrosine Phosphatase 1B Inhibitory Activity". Natural Product Communications 7, nr 7 (lipiec 2012): 1934578X1200700. http://dx.doi.org/10.1177/1934578x1200700701.
Pełny tekst źródłaAyer, William A., i Peter Craw. "Metabolites of the fairy ring fungus, Marasmiusoreades. Part 2. Norsesquiterpenes, further sesquiterpenes, and agrocybin". Canadian Journal of Chemistry 67, nr 9 (1.09.1989): 1371–80. http://dx.doi.org/10.1139/v89-210.
Pełny tekst źródłaLi, Li, Shenghui Yang, Dilu Chen, Zhihuang Wu, Meijun Zhang, Fang Yang, Li Qin i Xiaojiang Zhou. "In Vitro Anti-Influenza A Virus H1N1 Effect of Sesquiterpene-Rich Extracts of Carpesium abrotanoides". Molecules 27, nr 23 (29.11.2022): 8313. http://dx.doi.org/10.3390/molecules27238313.
Pełny tekst źródłaYan, Xiaoguang, Yukun Li, Weiguo Li, Dongmei Liang, Shengxin Nie, Ruiqi Chen, Jianjun Qiao, Mingzhang Wen i Qinggele Caiyin. "Transcriptome Analysis and Identification of Sesquiterpene Synthases in Liverwort Jungermannia exsertifolia". Bioengineering 10, nr 5 (9.05.2023): 569. http://dx.doi.org/10.3390/bioengineering10050569.
Pełny tekst źródłaZhang, Xu-Feng, Jie Ren, Xiang-Rong Cheng, Hui-Zi Jin i Wei-Dong Zhang. "One new unusual sesterterpenoid and four new sesquiterpene dimers from Inula britannica". RSC Advances 5, nr 3 (2015): 1979–82. http://dx.doi.org/10.1039/c4ra11171k.
Pełny tekst źródłaJerković, Igor, Željan Maleš i Maja Friščić. "Actualities in the phytochemical research on selected terpenes". Acta Pharmaceutica 69, nr 4 (1.12.2019): 533–40. http://dx.doi.org/10.2478/acph-2019-0036.
Pełny tekst źródłaLiang, Yi, Xiao-Ming Li, Chun-Shun Li, Hong Sun i Bin-Gui Wang. "Laurane-, Cyclolaurane-, and Cuparane-type Sesquiterpenes from the Marine Red Alga Laurencia okamurai". Natural Product Communications 9, nr 3 (marzec 2014): 1934578X1400900. http://dx.doi.org/10.1177/1934578x1400900310.
Pełny tekst źródłaRozprawy doktorskie na temat "Sesquiterpenes"
Henry, S. G. "Studies towards tricyclic sesquiterpenes". Thesis, University of Cambridge, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.603969.
Pełny tekst źródłaVieira, Tiago de Oliveira. "Estudos visando à síntese de sesquiterpenos bacanos". Universidade de São Paulo, 2005. http://www.teses.usp.br/teses/disponiveis/46/46135/tde-06062016-155559/.
Pełny tekst źródłaIn this thesis, we have developed studies towards the synthesis of sesquiterpenes bakkanes, which key step consisted on the construction of the cis-hydrindanic system through a thallium(III) mediated ring contraction reaction of cis-decalins and 2-octalones. Only the cis-octalins, such as the 1,2,3,4,4a,5,8,8a-octahydro-4a-methylnaphthalene and the 1,2,3,4,4a,5,8,8a-octahydro-4a,7-dimethylnaphthalene, were able to be ring contracted in satisfactory yields; the 4,4a,5,6,7,8-hexahydro-4a,5-dimethylnaphthalen-2(3H)-one, however, furnished the ring contraction product in low yield. We tried to use the reaction of 1,2,3,4,4a,5,8,8a-octahydro-4amethylnaphthalene with TTN in the synthesis of nor-bakkenolide-A, but we could not accomplish the synthesis because it was not possible to make the last step of the sequence, in all tested approaches. Great efforts were made in the diastereoselective preparation of the 4,4a,5,6, 7 ,8-hexahydro-4a,5-dimethylnaphthalen-2(3H)-one, through three different approaches that were investigated, being two of them with profit. However, the low yield (38%) of the ring contraction reaction of 4,4a,5,6, 7,8-hexahydro-4a,5-dimethylnaphthalen-2(3H)-one, precluded the continuation of the synthetic rout proposed to the bakkenolide-A. We have also performed the kinetic resolution of three different cis-octalols that were prepared through Diels-Alder reaction followed by diastereoselective reduction - with the Novozym 435 lipase, and the resolved products were isolated in excellent yields (≥ 40% for each enantiomer) and excellent ee\'s (≥ 98%).
伍冠先 i Koon-sin Ngo. "Synthesis isolation and autoxidation of sesquiterpenes". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1999. http://hub.hku.hk/bib/B31239134.
Pełny tekst źródłaPerea, Buceta Jesus E. "Synthetic studies on anislactone-type sesquiterpenes". Thesis, University of Edinburgh, 2007. http://hdl.handle.net/1842/15628.
Pełny tekst źródłaNgo, Koon-sin. "Synthesis isolation and autoxidation of sesquiterpenes /". Hong Kong : University of Hong Kong, 1999. http://sunzi.lib.hku.hk/hkuto/record.jsp?B2102103X.
Pełny tekst źródłaSarkar, Purabi. "Studies in the synthesis of sesquiterpenes". Thesis, University of North Bengal, 1992. http://hdl.handle.net/123456789/852.
Pełny tekst źródłaLeung, Pou Ian. "Sesquiterpenes emission from common airborne fungal species /". View abstract or full-text, 2009. http://library.ust.hk/cgi/db/thesis.pl?EVNG%202009%20LEUNG.
Pełny tekst źródłaVaidya, S. P. "Studies in sesquiterpenes: newer perspectives of longifolene". Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 1985. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/3238.
Pełny tekst źródłaSatyanarayana, N. "Studies in sesquiterpenes (newer aspects of longifolene)". Thesis(Ph.D.), CSIR-National Chemical Laboratory, Poona, 1985. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/3230.
Pełny tekst źródłaSelvakumar, N. "Synthetic investigations on terpenoids". Thesis, Indian Institute of Science, 1994. https://etd.iisc.ac.in/handle/2005/110.
Pełny tekst źródłaKsiążki na temat "Sesquiterpenes"
Breitmaier, E. Terpenes: Flavors, fragrances, pharmaca, pheromones. Weinheim, Germany: WILEY-VCH, 2006.
Znajdź pełny tekst źródłaKrahn, Ulrich. Gaschromatographisch-massenspektroskopische Untersuchungen der flüchtigen Stoffwechselprodukte des sesquiterpenbildenden Basidiomyceten Poria xantha. Berlin: P. Oberhofer, 1986.
Znajdź pełny tekst źródłaRichard, Beasley Val, red. Trichothecene mycotoxicosis: Pathophysiologic effects. Boca Raton, Fla: CRC Press, 1989.
Znajdź pełny tekst źródłaSülsen, Valeria Patricia, i Virginia Susana Martino, red. Sesquiterpene Lactones. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-78274-4.
Pełny tekst źródłaMorrissey, Brian Eamon. A study of the sesquiterpene aryl esters of armillaria species. Dublin: University College Dublin, 1997.
Znajdź pełny tekst źródłaSerkerov, Siradzhaddin Veli ogly. Terpenoidy i fenolproizvodnye rasteniĭ semeĭstv: Asteraceae i Apiaceae. Baku: CBS, 2005.
Znajdź pełny tekst źródłaSchreiner, Oswald. Sesquiterpenes: A Monograph. Creative Media Partners, LLC, 2018.
Znajdź pełny tekst źródłaCrock, John Edward. Five sesquiterpene synthases. 1998.
Znajdź pełny tekst źródłaPirrung, Michael C., David Goldsmith, Andrew T. Morehead i Andrew T. Jr Morehead. Total Synthesis of Natural Products: Acyclic and Monocyclic Sesquiterpenes. Wiley & Sons, Incorporated, John, 2009.
Znajdź pełny tekst źródłaPirrung, Michael C., David Goldsmith i Morehead Andrew T. Jr. Total Synthesis of Natural Products: Acyclic and Monocyclic Sesquiterpenes. Wiley & Sons, Incorporated, John, 2007.
Znajdź pełny tekst źródłaCzęści książek na temat "Sesquiterpenes"
Seigler, David S. "Sesquiterpenes". W Plant Secondary Metabolism, 367–97. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-4913-0_21.
Pełny tekst źródłaZografos, Alexandros L., i Elissavet E. Anagnostaki. "Sesquiterpenes". W From Biosynthesis to Total Synthesis, 236–78. Hoboken, NJ: John Wiley & Sons, Inc, 2016. http://dx.doi.org/10.1002/9781118754085.ch7.
Pełny tekst źródłaBanik, Bimal Krishna, Abhishek Tiwari i Biswa Mohan Sahoo. "Sesquiterpenes Lactone". W Terpenoids, 517–46. Boca Raton: CRC Press, 2022. http://dx.doi.org/10.1201/9781003008682-16.
Pełny tekst źródłaAtta-ur-Rahman i Viqar Uddin Ahmad. "Miscellaneous Sesquiterpenes". W 13C-NMR of Natural Products, 786–829. Boston, MA: Springer US, 1992. http://dx.doi.org/10.1007/978-1-4615-3290-3_79.
Pełny tekst źródłaSugita-Konishi, Yoshiko, i Makoto Kimura. "Nivalenol (Fungal Sesquiterpenes)". W Natural Products, 3123–57. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-22144-6_135.
Pełny tekst źródłaSharma, Ajay, Vivek K. Bajpai i Shruti Shukla. "Sesquiterpenes and Cytotoxicity". W Natural Products, 3515–50. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-22144-6_152.
Pełny tekst źródłaSchütte, Horst-Robert. "Secondary Plant Substances: Sesquiterpenes". W Progress in Botany, 341–65. Berlin, Heidelberg: Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/978-3-642-59940-8_13.
Pełny tekst źródłaNéri-Numa, Iramaia, Kele A. C. Vespermann, Carlos H. Carvalho, Bruno Nicolau Paulino, Maria J. Macedo, Gláucia M. Pastore, Juliano Lemos Bicas i Gustavo Molina. "Bioactive Potential of Sesquiterpenes". W Food Aroma Evolution, 695–718. 1st edition. | Boca Raton : CRC Press, 2019. | Series: Food analysis & properties, 2475-7551: CRC Press, 2019. http://dx.doi.org/10.1201/9780429441837-32.
Pełny tekst źródłaDurán, Alexandra G., Carlos Rial, M. Teresa Gutiérrez, José M. G. Molinillo i Francisco A. Macías. "Sesquiterpenes in Fresh Food". W Handbook of Dietary Phytochemicals, 1–66. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-1745-3_47-1.
Pełny tekst źródłaDurán, Alexandra G., Carlos Rial, M. Teresa Gutiérrez, José M. G. Molinillo i Francisco A. Macías. "Sesquiterpenes in Fresh Food". W Handbook of Dietary Phytochemicals, 477–542. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-15-4148-3_47.
Pełny tekst źródłaStreszczenia konferencji na temat "Sesquiterpenes"
Zlatic, Nenad, Vladimir Mihailovic, Gorica Đelic, Marija Ljesevic, Vladimir Beskoski i Milan Stankovic. "VARIJABILNOST SESKVITERPENA ETARSKIH ULJA VRSTE TEUCRIUM MONTANUM L." W XXVI savetovanje o biotehnologiji sa međunarodnim učešćem. University of Kragujevac, Faculty of Agronomy, 2021. http://dx.doi.org/10.46793/sbt26.453z.
Pełny tekst źródłaVasas, A., I. Lajter, P. Forgó, N. Kúsz, N. Bózsity, I. Zupkó, N. Nagy, G. Krupitza, R. Frish i J. Hohmann. "Sesquiterpenes from Neurolaena lobata with antiproliferative activity". W GA 2017 – Book of Abstracts. Georg Thieme Verlag KG, 2017. http://dx.doi.org/10.1055/s-0037-1608119.
Pełny tekst źródłaKim, J. S., J. R. Kim, H. A. Lim, C. H. Jang, J. H. Kim, Y. K. Kim, T. Konishi i J. Yoon Park. "Induction of Detoxifying Enzyme by Sesquiterpenes Present in Inula helenium". W 13th World Congress of Food Science & Technology. Les Ulis, France: EDP Sciences, 2006. http://dx.doi.org/10.1051/iufost:20060786.
Pełny tekst źródłaNejad Ebrahimi, S., H. Asadi, H. Esmaeili, A. Karami, J. Hadian, M. Hamburger i A. Chaanin. "Sesquiterpenes from Petasites hybridus rhizomes and determination absolute configuration by circular dichroism". W GA 2017 – Book of Abstracts. Georg Thieme Verlag KG, 2017. http://dx.doi.org/10.1055/s-0037-1608043.
Pełny tekst źródłaRamseyer, J., B. Thuerig, M. De Mieri, HJ Schärer, T. Oberhänsli, MP Gupta, L. Tamm, O. Potterat i M. Hamburger. "Eudesmane sesquiterpenes from Verbesina lanata with inhibitory activity against major agricultural pathogen". W GA 2017 – Book of Abstracts. Georg Thieme Verlag KG, 2017. http://dx.doi.org/10.1055/s-0037-1608186.
Pełny tekst źródłaKuck, K., B. Lipowicz, G. Jürgenliemk i J. Heilmann. "Isolation and structure elucidation of several tri- and sesquiterpenes from Commiphora myrrha (Nees) Engl." W 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-0039-3399896.
Pełny tekst źródłaDerita, M., M. Di Liberto i S. Zacchino. "Importance of the C9 absolute configuration for the antifungal activity of natural and semisynthetic sesquiterpenes". W Proceedings of the International Conference on Antimicrobial Research (ICAR2010). WORLD SCIENTIFIC, 2011. http://dx.doi.org/10.1142/9789814354868_0073.
Pełny tekst źródłaNeves, Valdete de Souza Silva, ADRIANA MARIA DE BRITO SILVA, ALZIRA APARECIDA DA SILVA i ROSÂNGELA LUDWIG CAPATTO. "COMPOSIÇÃO QUÍMICA DO ÓLEO ESSENCIAL OBTIDO DAS FOLHAS E CASCAS DA Nectandr mebranacea (SW.) Griseb (Lauraceae) COLETADA NO SUL DE MATO GROSSO DO SUL." W II Congresso Brasileiro de Biodiversidade Virtual. Revista Multidisciplinar de Educação e meio ambiente, 2022. http://dx.doi.org/10.51189/ii-conbiv/7117.
Pełny tekst źródłaRackov, Sanja, Aleksandra Nešić, Milan Vraneš i Branka Pilić. "DEVELOPMENT OF ELECTROSPUN POLY(VINYLPYRROLIDONE) (PVP) NANOFIBER MATS LOADED BY CALENDULA OFFICINALIS EXTRACT AND COENZYME Q10". W 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac, 2021. http://dx.doi.org/10.46793/iccbi21.169r.
Pełny tekst źródłaLungu, Lidia, Svetlana Blaja, Violeta Popescu, Alexandru Ciocarlan, Ion Dragalin i Aculina Aricu. "The dynamics of lavender and clary sage volatile oils adulteration on-air exposure". W Scientific seminar with international participation "New frontiers in natural product chemistry". Institute of Chemistry, Republic of Moldova, 2023. http://dx.doi.org/10.19261/nfnpc.2023.ab11.
Pełny tekst źródłaRaporty organizacyjne na temat "Sesquiterpenes"
Joel, Daniel M., John C. Steffens i Alfred M. Mayer. Host-Elicited Germination and Mechanism of Penetration in Broomrape (Orobanche Spp.). United States Department of Agriculture, sierpień 1993. http://dx.doi.org/10.32747/1993.7568107.bard.
Pełny tekst źródłaWestwood, James H., Yaakov Tadmor i Hanan Eizenberg. Identifying the genes involved in host root perception by root parasitic weeds: Genetic and transcriptomic analysis of Orobanche hybrids differing in signal response specificity. United States Department of Agriculture, styczeń 2013. http://dx.doi.org/10.32747/2013.7598145.bard.
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