Artículos de revistas sobre el tema "Santalenes"
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Yin, Jun-Lin y Woon-Seng Wong. "Production of santalenes and bergamotene in Nicotiana tabacum plants". PLOS ONE 14, n.º 1 (4 de enero de 2019): e0203249. http://dx.doi.org/10.1371/journal.pone.0203249.
Texto completoCheng, Qingwei, Yuping Xiong, Meiyun Niu, Yueya Zhang, Haifeng Yan, Hanzhi Liang, Beiyi Guo et al. "Callus of East Indian sandalwood co-cultured with fungus Colletotrichum gloeosporioides accumulates santalenes and bisabolene". Trees 33, n.º 1 (14 de septiembre de 2018): 305–12. http://dx.doi.org/10.1007/s00468-018-1758-0.
Texto completoArai, Yoshitsugu, Masatoshi Yamamoto y Toru Koizumi. "Enantioselective Synthesis of the Functionalized Bicyclo[2.2.1]heptane Derivatives, Key Intermediates for the Chiral Synthesis of Santalenes and Santalols". Chemistry Letters 15, n.º 7 (5 de julio de 1986): 1225–28. http://dx.doi.org/10.1246/cl.1986.1225.
Texto completoDaramwar, Pankaj P., Prabhakar Lal Srivastava, Balaraman Priyadarshini y Hirekodathakallu V. Thulasiram. "Preparative separation of α- and β-santalenes and (Z)-α- and (Z)-β-santalols using silver nitrate-impregnated silica gel medium pressure liquid chromatography and analysis of sandalwood oil". Analyst 137, n.º 19 (2012): 4564. http://dx.doi.org/10.1039/c2an35575b.
Texto completoNgo, Koon-Sin y Geoffrey D. Brown. "Autoxidation of α-santalene". Journal of Chemical Research 2000, n.º 2 (febrero de 2000): 68–70. http://dx.doi.org/10.3184/030823400103166599.
Texto completoUnnikrishnan, P. A. y P. A. Vatakencherry. "Syntheses of epi-β-Santalene, β-Santalene and an Isomer of β-Santalene with 4-Methyl-4-pentenyl Side Chain". Synthetic Communications 22, n.º 22 (diciembre de 1992): 3159–68. http://dx.doi.org/10.1080/00397919208021129.
Texto completoUNNIKRISHNAN, P. A. y P. A. VATAKENCHERRY. "ChemInform Abstract: Synthesis of epi-β-Santalene (I), β-Santalene (II), and an Isomer (III) of β-Santalene with 4-Methyl-4-pentenyl Side Chain." ChemInform 24, n.º 18 (20 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199318271.
Texto completoTakano, Seiichi, Kohei Inomata, Ayako Kurotaki, Takehiko Ohkawa y Kunio Ogasawara. "Enantiodivergent route to both enantiomers of β-santalene and epi-β-santalene from a single chiral template". J. Chem. Soc., Chem. Commun., n.º 22 (1987): 1720–22. http://dx.doi.org/10.1039/c39870001720.
Texto completoGuo, Shan-Shan, Yang Wang, Zhen-Yang Chen, Zhe Zhang, Ju-Qin Cao, Xue Pang, Zhu-Feng Geng y Shu-Shan Du. "Essential Oils from Clausena Species in China: Santalene Sesquiterpenes Resource and Toxicity against Liposcelis bostrychophila". Journal of Chemistry 2018 (19 de noviembre de 2018): 1–8. http://dx.doi.org/10.1155/2018/7813675.
Texto completoKelsey, Rick G., Ovid McCuistion y Joe Karchesy. "Bark and Leaf Essential Oil of Umbellularia californica, California Bay Laurel, from Oregon". Natural Product Communications 2, n.º 7 (julio de 2007): 1934578X0700200. http://dx.doi.org/10.1177/1934578x0700200715.
Texto completoSaito, Masanori, Mitsuhiro Kawamura y Kunio Ogasawara. "Diastereo and enantio-controlled synthesis of sandalwood constituents (-)-β-santalene and (+)-epi-β-santalene starting from the same (+)-norcamphor". Tetrahedron Letters 36, n.º 49 (diciembre de 1995): 9003–6. http://dx.doi.org/10.1016/0040-4039(95)01971-j.
Texto completoAhmed, Muniruddin, Bidyut Kanti Datta, A. S. S. Rouf y Jasmin Jakupovic. "Flavone and α-santalene derivatives from Polygonum flaccidum". Phytochemistry 30, n.º 9 (enero de 1991): 3155–56. http://dx.doi.org/10.1016/s0031-9422(00)98279-7.
Texto completoSAITO, M., M. KAWAMURA y K. OGASAWARA. "ChemInform Abstract: Diastereo- and Enantio-Controlled Synthesis of Sandalwood Constituents (-)-β-Santalene and (+)-Epi-β-santalene Starting from the Same (+)-Norcamphor." ChemInform 27, n.º 13 (12 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199613213.
Texto completoTravaini, Lucia. "Les frontières de l'Éternité ? Le cas d'un nom de monnaie : santalene". Revue numismatique 6, n.º 164 (2008): 169–83. http://dx.doi.org/10.3406/numi.2008.2849.
Texto completoUnnikrishnan, P. A. "A HIGHLY STEREOSELECTIVE TRANSFORMATION OF β-SANTALENE TO (E)-β-SANTALOL". Organic Preparations and Procedures International 26, n.º 4 (agosto de 1994): 488–91. http://dx.doi.org/10.1080/00304949409458045.
Texto completoHua, Gaoqun, Yiling Hu, Chunyu Yang, Dazhi Liu, Zhuo Mao, Lixin Zhang y Yan Zhang. "Characterization of santalene synthases using an inorganic pyrophosphatase coupled colorimetric assay". Analytical Biochemistry 547 (abril de 2018): 26–36. http://dx.doi.org/10.1016/j.ab.2018.02.002.
Texto completoMuñoz, Orlando, Phlippe Christen, Silvian Cretton, Alejandro F. Barrero, Armando Lara y M. Mar Herrador. "Comparison of the Essential Oils of Leaves and Stem Bark from Two Different Populations of Drimys Winteri a Chilean Herbal Medicine". Natural Product Communications 6, n.º 6 (junio de 2011): 1934578X1100600. http://dx.doi.org/10.1177/1934578x1100600630.
Texto completoVerdan, Maria Helena, Carlos Augusto Ehrenfried, Dilamara Riva Scharf, Armando Carlos Cervi, Marcos José Salvador, Andersson Barison y Maria Elida A. Stefanello. "Chemical Constituents from Sinningia canescens and S. warmingii". Natural Product Communications 9, n.º 10 (octubre de 2014): 1934578X1400901. http://dx.doi.org/10.1177/1934578x1400901033.
Texto completoJia, Dan, Shuo Xu, Jie Sun, Chuanbo Zhang, Dashuai Li y Wenyu Lu. "Yarrowia lipolytica construction for heterologous synthesis of α-santalene and fermentation optimization". Applied Microbiology and Biotechnology 103, n.º 8 (12 de marzo de 2019): 3511–20. http://dx.doi.org/10.1007/s00253-019-09735-w.
Texto completoWeston, Roderick J. y Gerald J. Smith. "Sesquiterpenes from the Inner Bark of the Silver Birch and the Paper Birch". Natural Product Communications 7, n.º 2 (febrero de 2012): 1934578X1200700. http://dx.doi.org/10.1177/1934578x1200700202.
Texto completoUNNIKRISHNAN, P. A. "ChemInform Abstract: A Highly Stereoselective Transformation of β-Santalene into (E)-. beta.-Santalol." ChemInform 26, n.º 5 (18 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199505224.
Texto completoTippmann, Stefan, Gionata Scalcinati, Verena Siewers y Jens Nielsen. "Production of farnesene and santalene bySaccharomyces cerevisiaeusing fed-batch cultivations withRQ-controlled feed". Biotechnology and Bioengineering 113, n.º 1 (2 de septiembre de 2015): 72–81. http://dx.doi.org/10.1002/bit.25683.
Texto completoThang, Tran D., Do N. Dai, Tran M. Hoi y Isiaka A. Ogunwande. "Essential Oils from Five Species of Annonaceae from Vietnam". Natural Product Communications 8, n.º 2 (febrero de 2013): 1934578X1300800. http://dx.doi.org/10.1177/1934578x1300800228.
Texto completoAryal, Hari Prasad y Usha Budathoki. "Systematics of Nepalese Termitomyces". Our Nature 13, n.º 1 (27 de diciembre de 2015): 31–44. http://dx.doi.org/10.3126/on.v13i1.14207.
Texto completoJindal, Garima y Raghavan B. Sunoj. "Revisiting sesquiterpene biosynthetic pathways leading to santalene and its analogues: a comprehensive mechanistic study". Organic & Biomolecular Chemistry 10, n.º 39 (2012): 7996. http://dx.doi.org/10.1039/c2ob26027a.
Texto completoKloster, Adriana C. y Silvia C. Gnaedinger. "Coniferous wood of Agathoxylon from the La Matilde Formation, (Middle Jurassic), Santa Cruz, Argentina". Journal of Paleontology 92, n.º 4 (2 de abril de 2018): 546–67. http://dx.doi.org/10.1017/jpa.2017.145.
Texto completoDi Girolamo, Alice, Janani Durairaj, Adèle van Houwelingen, Francel Verstappen, Dirk Bosch, Katarina Cankar, Harro Bouwmeester, Dick de Ridder, Aalt D. J. van Dijk y Jules Beekwilder. "The santalene synthase from Cinnamomum camphora: Reconstruction of a sesquiterpene synthase from a monoterpene synthase". Archives of Biochemistry and Biophysics 695 (noviembre de 2020): 108647. http://dx.doi.org/10.1016/j.abb.2020.108647.
Texto completoMordini, Alessandro, Sabina Pecchi y Giuseppe Capozzi. "The synthesis of 4′-thia-α-santalene and 4′-thia-α-santalol through an organometallic approach". Tetrahedron 50, n.º 20 (enero de 1994): 6029–36. http://dx.doi.org/10.1016/s0040-4020(01)90455-7.
Texto completoKrotz, Achim y Günter Helmchen. "Total syntheses of sandalwood fragrances: (Z)- and (E)-β-santalol and their enantiomers, ent-β-santalene". Tetrahedron: Asymmetry 1, n.º 8 (enero de 1990): 537–40. http://dx.doi.org/10.1016/s0957-4166(00)80544-3.
Texto completoOppolzer, Wolfgang, Christian Chapuis, Dominique Dupuis y Maodao Guo. "AsymmetricDiels-Alder Reactions of Neopentyl-Ether-Shielded Acrylates and Allenic Esters: Syntheses of (?)-Norbornenone and (?)-?-Santalene". Helvetica Chimica Acta 68, n.º 8 (18 de diciembre de 1985): 2100–2114. http://dx.doi.org/10.1002/hlca.19850680803.
Texto completoZhong, Guo-fu y Manfred Schlosser. "4′-Oxa-α-santalene and 4′-oxa-α-santalol : An olfactory comparison with the analogous natural sesquiterpenes". Tetrahedron Letters 34, n.º 39 (septiembre de 1993): 6265–68. http://dx.doi.org/10.1016/s0040-4039(00)73727-0.
Texto completoScalcinati, Gionata, Siavash Partow, Verena Siewers, Michel Schalk, Laurent Daviet y Jens Nielsen. "Combined metabolic engineering of precursor and co-factor supply to increase α-santalene production by Saccharomyces cerevisiae". Microbial Cell Factories 11, n.º 1 (2012): 117. http://dx.doi.org/10.1186/1475-2859-11-117.
Texto completoZhong, Guo-fu y Manfred Schlosser. "A Short and Simple Access to Both Enantiomers of Epi-β-santalene and (Z)-Epi-β-santalol". Synlett 1994, n.º 03 (1994): 173–74. http://dx.doi.org/10.1055/s-1994-22781.
Texto completoKamikubo, Takashi y Kunio Ogasawara. "Preparation of (+)-Tricyclo[6.2.1.02,7]undec-2(7)-en-3-one and Its Conversion into (+)-epi-β-Santalene". Chemistry Letters 24, n.º 2 (febrero de 1995): 95–96. http://dx.doi.org/10.1246/cl.1995.95.
Texto completoMORDINI, A., S. PECCHI y G. CAPOZZI. "ChemInform Abstract: Synthesis of 4′-Thia-α-santalene and 4′-Thia-α-santalol Through an Organometallic Approach." ChemInform 25, n.º 39 (18 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199439232.
Texto completoCoulerie, Paul, Louis Thouvenot, Mohammed Nour y Yoshinori Asakawa. "Chemical Originalities of New Caledonian Liverworts from Lejeuneaceae Family". Natural Product Communications 10, n.º 9 (septiembre de 2015): 1934578X1501000. http://dx.doi.org/10.1177/1934578x1501000903.
Texto completoZHONG, G. F. y M. SCHLOSSER. "ChemInform Abstract: A Short and Simple Access to Both Enantiomers of Epi-β-santalene and (Z)-Epi-β-santalol." ChemInform 25, n.º 34 (19 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199434206.
Texto completoKAMIKUBO, T. y K. OGASAWARA. "ChemInform Abstract: Preparation of (+)-Tricyclo(6.2.1.02,7)undec-2(7)-en-3-one and Its Conversion into (+)-epi-β-Santalene." ChemInform 26, n.º 29 (17 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199529250.
Texto completoBaldovini, Nicolas y Guy Solladié. "Application of the asymmetric Diels–Alder reaction of a 2-substituted chiral maleate to the formal synthesis of (−)-β-santalene". Tetrahedron: Asymmetry 13, n.º 8 (mayo de 2002): 885–89. http://dx.doi.org/10.1016/s0957-4166(02)00194-5.
Texto completoJones, Christopher G., Jessie Moniodis, Katherine G. Zulak, Adrian Scaffidi, Julie A. Plummer, Emilio L. Ghisalberti, Elizabeth L. Barbour y Jörg Bohlmann. "Sandalwood fragrance biosynthesis involves sesquiterpene synthases of both the terpene synthase (TPS)-a and TPS-b subfamilies, including santalene synthases." Journal of Biological Chemistry 287, n.º 45 (2 de noviembre de 2012): 37713–14. http://dx.doi.org/10.1074/jbc.a111.231787.
Texto completoJones, Christopher G., Jessie Moniodis, Katherine G. Zulak, Adrian Scaffidi, Julie A. Plummer, Emilio L. Ghisalberti, Elizabeth L. Barbour y Jörg Bohlmann. "Sandalwood Fragrance Biosynthesis Involves Sesquiterpene Synthases of Both the Terpene Synthase (TPS)-a and TPS-b Subfamilies, including Santalene Synthases". Journal of Biological Chemistry 286, n.º 20 (24 de marzo de 2011): 17445–54. http://dx.doi.org/10.1074/jbc.m111.231787.
Texto completoBarton, Dustin y James Chickos. "Vaporization enthalpies and vapor pressures of the major components of opopanax oil, α-santalene, cis α-bisabolene, cis α-bergamotene". Structural Chemistry 32, n.º 3 (24 de marzo de 2021): 939–52. http://dx.doi.org/10.1007/s11224-021-01764-4.
Texto completoKrotz, Achim y Günter Helmchen. "Total Syntheses, Optical Rotations and Fragrance Properties of Sandalwood Constituents: (−)-(Z)- and (−)-(E)-β-Santalol and Their Enantiomers,ent-β-Santalene". Liebigs Annalen der Chemie 1994, n.º 6 (13 de junio de 1994): 601–9. http://dx.doi.org/10.1002/jlac.199419940610.
Texto completoMuturi, Ephantus J., William T. Hay, Kenneth M. Doll, Jose L. Ramirez y Gordon Selling. "Insecticidal Activity of Commiphora erythraea Essential Oil and Its Emulsions Against Larvae of Three Mosquito Species". Journal of Medical Entomology 57, n.º 6 (30 de mayo de 2020): 1835–42. http://dx.doi.org/10.1093/jme/tjaa097.
Texto completoChen, Yanhang, Musavvara Kh Shukurova, Yonathan Asikin, Miyako Kusano y Kazuo N. Watanabe. "Characterization of Volatile Organic Compounds in Mango Ginger (Curcuma amada Roxb.) from Myanmar". Metabolites 11, n.º 1 (30 de diciembre de 2020): 21. http://dx.doi.org/10.3390/metabo11010021.
Texto completoRoussis, Vassilios, Constantinos Vagias, Christina Tsitsimpikou y Nina Diamantopoulou. "Chemical Variability of the Volatile Metabolites from the Caribbean Corals of the Genus Gorgonia". Zeitschrift für Naturforschung C 55, n.º 5-6 (1 de junio de 2000): 431–41. http://dx.doi.org/10.1515/znc-2000-5-620.
Texto completoScalcinati, Gionata, Christoph Knuf, Siavash Partow, Yun Chen, Jérôme Maury, Michel Schalk, Laurent Daviet, Jens Nielsen y Verena Siewers. "Dynamic control of gene expression in Saccharomyces cerevisiae engineered for the production of plant sesquitepene α-santalene in a fed-batch mode". Metabolic Engineering 14, n.º 2 (marzo de 2012): 91–103. http://dx.doi.org/10.1016/j.ymben.2012.01.007.
Texto completoKROTZ, A. y G. HELMCHEN. "ChemInform Abstract: Total Syntheses, Optical Rotations and Fragrance Properties of Sandalwood Constituents: (-)-(Z)- and (-)-(E)-β-Santalol and Their Enantiomers, ent-β-Santalene." ChemInform 25, n.º 45 (18 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199445192.
Texto completoJuvik, John A. "IMPROVED HOST PLANT RESISTANCE BY MODIFICATION OF PLANT CHEMICAL CUES ASSOCIATED WITH HELIOTHIS ZEA HOST PLANT SELECTION FOR OVIPOSITION". HortScience 25, n.º 9 (septiembre de 1990): 1178a—1178. http://dx.doi.org/10.21273/hortsci.25.9.1178a.
Texto completoTanase, Corneliu, Ruxandra Ștefănescu, Béla Darkó, Daniela Lucia Muntean, Anca Corina Fărcaş y Sonia Ancuţa Socaci. "Biochemical and Histo-Anatomical Responses of Lavandula angustifolia Mill. to Spruce and Beech Bark Extracts Application". Plants 9, n.º 7 (7 de julio de 2020): 859. http://dx.doi.org/10.3390/plants9070859.
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