Literatura académica sobre el tema "Sesquiterpenes"
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Artículos de revistas sobre el tema "Sesquiterpenes"
Coca-Ruíz, Víctor, Ivonne Suárez, Josefina Aleu y Isidro G. Collado. "Structures, Occurrences and Biosynthesis of 11,12,13-Tri-nor-Sesquiterpenes, an Intriguing Class of Bioactive Metabolites". Plants 11, n.º 6 (14 de marzo de 2022): 769. http://dx.doi.org/10.3390/plants11060769.
Texto completoSilva, Waldeyr M. C. da, Jakob L. Andersen, Maristela T. Holanda, Maria Emília M. T. Walter, Marcelo M. Brigido, Peter F. Stadler y Christoph Flamm. "Exploring Plant Sesquiterpene Diversity by Generating Chemical Networks". Processes 7, n.º 4 (25 de abril de 2019): 240. http://dx.doi.org/10.3390/pr7040240.
Texto completoWang, Junchi, Qi Zheng, Huaxiang Wang, Leiling Shi, Guoping Wang, Yaqin Zhao, Congzhao Fan y Jianyong Si. "Sesquiterpenes and Sesquiterpene Derivatives from Ferula: Their Chemical Structures, Biosynthetic Pathways, and Biological Properties". Antioxidants 13, n.º 1 (19 de diciembre de 2023): 7. http://dx.doi.org/10.3390/antiox13010007.
Texto completoSaifudin, Azis, Ken Tanaka, Shigetoshi Kadota y Yasuhiro Tezuka. "Chemical Constituents of Blumea balsamifera of Indonesia and Their Protein Tyrosine Phosphatase 1B Inhibitory Activity". Natural Product Communications 7, n.º 7 (julio de 2012): 1934578X1200700. http://dx.doi.org/10.1177/1934578x1200700701.
Texto completoAyer, William A. y Peter Craw. "Metabolites of the fairy ring fungus, Marasmiusoreades. Part 2. Norsesquiterpenes, further sesquiterpenes, and agrocybin". Canadian Journal of Chemistry 67, n.º 9 (1 de septiembre de 1989): 1371–80. http://dx.doi.org/10.1139/v89-210.
Texto completoLi, Li, Shenghui Yang, Dilu Chen, Zhihuang Wu, Meijun Zhang, Fang Yang, Li Qin y Xiaojiang Zhou. "In Vitro Anti-Influenza A Virus H1N1 Effect of Sesquiterpene-Rich Extracts of Carpesium abrotanoides". Molecules 27, n.º 23 (29 de noviembre de 2022): 8313. http://dx.doi.org/10.3390/molecules27238313.
Texto completoYan, Xiaoguang, Yukun Li, Weiguo Li, Dongmei Liang, Shengxin Nie, Ruiqi Chen, Jianjun Qiao, Mingzhang Wen y Qinggele Caiyin. "Transcriptome Analysis and Identification of Sesquiterpene Synthases in Liverwort Jungermannia exsertifolia". Bioengineering 10, n.º 5 (9 de mayo de 2023): 569. http://dx.doi.org/10.3390/bioengineering10050569.
Texto completoZhang, Xu-Feng, Jie Ren, Xiang-Rong Cheng, Hui-Zi Jin y Wei-Dong Zhang. "One new unusual sesterterpenoid and four new sesquiterpene dimers from Inula britannica". RSC Advances 5, n.º 3 (2015): 1979–82. http://dx.doi.org/10.1039/c4ra11171k.
Texto completoJerković, Igor, Željan Maleš y Maja Friščić. "Actualities in the phytochemical research on selected terpenes". Acta Pharmaceutica 69, n.º 4 (1 de diciembre de 2019): 533–40. http://dx.doi.org/10.2478/acph-2019-0036.
Texto completoLiang, Yi, Xiao-Ming Li, Chun-Shun Li, Hong Sun y Bin-Gui Wang. "Laurane-, Cyclolaurane-, and Cuparane-type Sesquiterpenes from the Marine Red Alga Laurencia okamurai". Natural Product Communications 9, n.º 3 (marzo de 2014): 1934578X1400900. http://dx.doi.org/10.1177/1934578x1400900310.
Texto completoTesis sobre el tema "Sesquiterpenes"
Henry, S. G. "Studies towards tricyclic sesquiterpenes". Thesis, University of Cambridge, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.603969.
Texto completoVieira, 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/.
Texto completoIn 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 y 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.
Texto completoPerea, Buceta Jesus E. "Synthetic studies on anislactone-type sesquiterpenes". Thesis, University of Edinburgh, 2007. http://hdl.handle.net/1842/15628.
Texto completoNgo, Koon-sin. "Synthesis isolation and autoxidation of sesquiterpenes /". Hong Kong : University of Hong Kong, 1999. http://sunzi.lib.hku.hk/hkuto/record.jsp?B2102103X.
Texto completoSarkar, Purabi. "Studies in the synthesis of sesquiterpenes". Thesis, University of North Bengal, 1992. http://hdl.handle.net/123456789/852.
Texto completoLeung, 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.
Texto completoVaidya, 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.
Texto completoSatyanarayana, 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.
Texto completoSelvakumar, N. "Synthetic investigations on terpenoids". Thesis, Indian Institute of Science, 1994. https://etd.iisc.ac.in/handle/2005/110.
Texto completoLibros sobre el tema "Sesquiterpenes"
Breitmaier, E. Terpenes: Flavors, fragrances, pharmaca, pheromones. Weinheim, Germany: WILEY-VCH, 2006.
Buscar texto completoKrahn, Ulrich. Gaschromatographisch-massenspektroskopische Untersuchungen der flüchtigen Stoffwechselprodukte des sesquiterpenbildenden Basidiomyceten Poria xantha. Berlin: P. Oberhofer, 1986.
Buscar texto completoRichard, Beasley Val, ed. Trichothecene mycotoxicosis: Pathophysiologic effects. Boca Raton, Fla: CRC Press, 1989.
Buscar texto completoSülsen, Valeria Patricia y Virginia Susana Martino, eds. Sesquiterpene Lactones. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-78274-4.
Texto completoMorrissey, Brian Eamon. A study of the sesquiterpene aryl esters of armillaria species. Dublin: University College Dublin, 1997.
Buscar texto completoSerkerov, Siradzhaddin Veli ogly. Terpenoidy i fenolproizvodnye rasteniĭ semeĭstv: Asteraceae i Apiaceae. Baku: CBS, 2005.
Buscar texto completoSchreiner, Oswald. Sesquiterpenes: A Monograph. Creative Media Partners, LLC, 2018.
Buscar texto completoCrock, John Edward. Five sesquiterpene synthases. 1998.
Buscar texto completoPirrung, Michael C., David Goldsmith, Andrew T. Morehead y Andrew T. Jr Morehead. Total Synthesis of Natural Products: Acyclic and Monocyclic Sesquiterpenes. Wiley & Sons, Incorporated, John, 2009.
Buscar texto completoPirrung, Michael C., David Goldsmith y Morehead Andrew T. Jr. Total Synthesis of Natural Products: Acyclic and Monocyclic Sesquiterpenes. Wiley & Sons, Incorporated, John, 2007.
Buscar texto completoCapítulos de libros sobre el tema "Sesquiterpenes"
Seigler, David S. "Sesquiterpenes". En Plant Secondary Metabolism, 367–97. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-4913-0_21.
Texto completoZografos, Alexandros L. y Elissavet E. Anagnostaki. "Sesquiterpenes". En From Biosynthesis to Total Synthesis, 236–78. Hoboken, NJ: John Wiley & Sons, Inc, 2016. http://dx.doi.org/10.1002/9781118754085.ch7.
Texto completoBanik, Bimal Krishna, Abhishek Tiwari y Biswa Mohan Sahoo. "Sesquiterpenes Lactone". En Terpenoids, 517–46. Boca Raton: CRC Press, 2022. http://dx.doi.org/10.1201/9781003008682-16.
Texto completoAtta-ur-Rahman y Viqar Uddin Ahmad. "Miscellaneous Sesquiterpenes". En 13C-NMR of Natural Products, 786–829. Boston, MA: Springer US, 1992. http://dx.doi.org/10.1007/978-1-4615-3290-3_79.
Texto completoSugita-Konishi, Yoshiko y Makoto Kimura. "Nivalenol (Fungal Sesquiterpenes)". En Natural Products, 3123–57. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-22144-6_135.
Texto completoSharma, Ajay, Vivek K. Bajpai y Shruti Shukla. "Sesquiterpenes and Cytotoxicity". En Natural Products, 3515–50. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-22144-6_152.
Texto completoSchütte, Horst-Robert. "Secondary Plant Substances: Sesquiterpenes". En Progress in Botany, 341–65. Berlin, Heidelberg: Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/978-3-642-59940-8_13.
Texto completoNéri-Numa, Iramaia, Kele A. C. Vespermann, Carlos H. Carvalho, Bruno Nicolau Paulino, Maria J. Macedo, Gláucia M. Pastore, Juliano Lemos Bicas y Gustavo Molina. "Bioactive Potential of Sesquiterpenes". En 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.
Texto completoDurán, Alexandra G., Carlos Rial, M. Teresa Gutiérrez, José M. G. Molinillo y Francisco A. Macías. "Sesquiterpenes in Fresh Food". En Handbook of Dietary Phytochemicals, 1–66. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-1745-3_47-1.
Texto completoDurán, Alexandra G., Carlos Rial, M. Teresa Gutiérrez, José M. G. Molinillo y Francisco A. Macías. "Sesquiterpenes in Fresh Food". En Handbook of Dietary Phytochemicals, 477–542. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-15-4148-3_47.
Texto completoActas de conferencias sobre el tema "Sesquiterpenes"
Zlatic, Nenad, Vladimir Mihailovic, Gorica Đelic, Marija Ljesevic, Vladimir Beskoski y Milan Stankovic. "VARIJABILNOST SESKVITERPENA ETARSKIH ULJA VRSTE TEUCRIUM MONTANUM L." En XXVI savetovanje o biotehnologiji sa međunarodnim učešćem. University of Kragujevac, Faculty of Agronomy, 2021. http://dx.doi.org/10.46793/sbt26.453z.
Texto completoVasas, A., I. Lajter, P. Forgó, N. Kúsz, N. Bózsity, I. Zupkó, N. Nagy, G. Krupitza, R. Frish y J. Hohmann. "Sesquiterpenes from Neurolaena lobata with antiproliferative activity". En GA 2017 – Book of Abstracts. Georg Thieme Verlag KG, 2017. http://dx.doi.org/10.1055/s-0037-1608119.
Texto completoKim, J. S., J. R. Kim, H. A. Lim, C. H. Jang, J. H. Kim, Y. K. Kim, T. Konishi y J. Yoon Park. "Induction of Detoxifying Enzyme by Sesquiterpenes Present in Inula helenium". En 13th World Congress of Food Science & Technology. Les Ulis, France: EDP Sciences, 2006. http://dx.doi.org/10.1051/iufost:20060786.
Texto completoNejad Ebrahimi, S., H. Asadi, H. Esmaeili, A. Karami, J. Hadian, M. Hamburger y A. Chaanin. "Sesquiterpenes from Petasites hybridus rhizomes and determination absolute configuration by circular dichroism". En GA 2017 – Book of Abstracts. Georg Thieme Verlag KG, 2017. http://dx.doi.org/10.1055/s-0037-1608043.
Texto completoRamseyer, J., B. Thuerig, M. De Mieri, HJ Schärer, T. Oberhänsli, MP Gupta, L. Tamm, O. Potterat y M. Hamburger. "Eudesmane sesquiterpenes from Verbesina lanata with inhibitory activity against major agricultural pathogen". En GA 2017 – Book of Abstracts. Georg Thieme Verlag KG, 2017. http://dx.doi.org/10.1055/s-0037-1608186.
Texto completoKuck, K., B. Lipowicz, G. Jürgenliemk y J. Heilmann. "Isolation and structure elucidation of several tri- and sesquiterpenes from Commiphora myrrha (Nees) Engl." En 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.
Texto completoDerita, M., M. Di Liberto y S. Zacchino. "Importance of the C9 absolute configuration for the antifungal activity of natural and semisynthetic sesquiterpenes". En Proceedings of the International Conference on Antimicrobial Research (ICAR2010). WORLD SCIENTIFIC, 2011. http://dx.doi.org/10.1142/9789814354868_0073.
Texto completoNeves, Valdete de Souza Silva, ADRIANA MARIA DE BRITO SILVA, ALZIRA APARECIDA DA SILVA y 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." En II Congresso Brasileiro de Biodiversidade Virtual. Revista Multidisciplinar de Educação e meio ambiente, 2022. http://dx.doi.org/10.51189/ii-conbiv/7117.
Texto completoRackov, Sanja, Aleksandra Nešić, Milan Vraneš y Branka Pilić. "DEVELOPMENT OF ELECTROSPUN POLY(VINYLPYRROLIDONE) (PVP) NANOFIBER MATS LOADED BY CALENDULA OFFICINALIS EXTRACT AND COENZYME Q10". En 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac, 2021. http://dx.doi.org/10.46793/iccbi21.169r.
Texto completoLungu, Lidia, Svetlana Blaja, Violeta Popescu, Alexandru Ciocarlan, Ion Dragalin y Aculina Aricu. "The dynamics of lavender and clary sage volatile oils adulteration on-air exposure". En 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.
Texto completoInformes sobre el tema "Sesquiterpenes"
Joel, Daniel M., John C. Steffens y Alfred M. Mayer. Host-Elicited Germination and Mechanism of Penetration in Broomrape (Orobanche Spp.). United States Department of Agriculture, agosto de 1993. http://dx.doi.org/10.32747/1993.7568107.bard.
Texto completoWestwood, James H., Yaakov Tadmor y 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, enero de 2013. http://dx.doi.org/10.32747/2013.7598145.bard.
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