Journal articles on the topic 'Santalenes'
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Yin, Jun-Lin, and Woon-Seng Wong. "Production of santalenes and bergamotene in Nicotiana tabacum plants." PLOS ONE 14, no. 1 (January 4, 2019): e0203249. http://dx.doi.org/10.1371/journal.pone.0203249.
Full textCheng, 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, no. 1 (September 14, 2018): 305–12. http://dx.doi.org/10.1007/s00468-018-1758-0.
Full textArai, Yoshitsugu, Masatoshi Yamamoto, and 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, no. 7 (July 5, 1986): 1225–28. http://dx.doi.org/10.1246/cl.1986.1225.
Full textDaramwar, Pankaj P., Prabhakar Lal Srivastava, Balaraman Priyadarshini, and 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, no. 19 (2012): 4564. http://dx.doi.org/10.1039/c2an35575b.
Full textNgo, Koon-Sin, and Geoffrey D. Brown. "Autoxidation of α-santalene." Journal of Chemical Research 2000, no. 2 (February 2000): 68–70. http://dx.doi.org/10.3184/030823400103166599.
Full textUnnikrishnan, P. A., and 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, no. 22 (December 1992): 3159–68. http://dx.doi.org/10.1080/00397919208021129.
Full textUNNIKRISHNAN, P. A., and 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, no. 18 (August 20, 2010): no. http://dx.doi.org/10.1002/chin.199318271.
Full textTakano, Seiichi, Kohei Inomata, Ayako Kurotaki, Takehiko Ohkawa, and Kunio Ogasawara. "Enantiodivergent route to both enantiomers of β-santalene and epi-β-santalene from a single chiral template." J. Chem. Soc., Chem. Commun., no. 22 (1987): 1720–22. http://dx.doi.org/10.1039/c39870001720.
Full textGuo, Shan-Shan, Yang Wang, Zhen-Yang Chen, Zhe Zhang, Ju-Qin Cao, Xue Pang, Zhu-Feng Geng, and Shu-Shan Du. "Essential Oils from Clausena Species in China: Santalene Sesquiterpenes Resource and Toxicity against Liposcelis bostrychophila." Journal of Chemistry 2018 (November 19, 2018): 1–8. http://dx.doi.org/10.1155/2018/7813675.
Full textKelsey, Rick G., Ovid McCuistion, and Joe Karchesy. "Bark and Leaf Essential Oil of Umbellularia californica, California Bay Laurel, from Oregon." Natural Product Communications 2, no. 7 (July 2007): 1934578X0700200. http://dx.doi.org/10.1177/1934578x0700200715.
Full textSaito, Masanori, Mitsuhiro Kawamura, and Kunio Ogasawara. "Diastereo and enantio-controlled synthesis of sandalwood constituents (-)-β-santalene and (+)-epi-β-santalene starting from the same (+)-norcamphor." Tetrahedron Letters 36, no. 49 (December 1995): 9003–6. http://dx.doi.org/10.1016/0040-4039(95)01971-j.
Full textAhmed, Muniruddin, Bidyut Kanti Datta, A. S. S. Rouf, and Jasmin Jakupovic. "Flavone and α-santalene derivatives from Polygonum flaccidum." Phytochemistry 30, no. 9 (January 1991): 3155–56. http://dx.doi.org/10.1016/s0031-9422(00)98279-7.
Full textSAITO, M., M. KAWAMURA, and 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, no. 13 (August 12, 2010): no. http://dx.doi.org/10.1002/chin.199613213.
Full textTravaini, Lucia. "Les frontières de l'Éternité ? Le cas d'un nom de monnaie : santalene." Revue numismatique 6, no. 164 (2008): 169–83. http://dx.doi.org/10.3406/numi.2008.2849.
Full textUnnikrishnan, P. A. "A HIGHLY STEREOSELECTIVE TRANSFORMATION OF β-SANTALENE TO (E)-β-SANTALOL." Organic Preparations and Procedures International 26, no. 4 (August 1994): 488–91. http://dx.doi.org/10.1080/00304949409458045.
Full textHua, Gaoqun, Yiling Hu, Chunyu Yang, Dazhi Liu, Zhuo Mao, Lixin Zhang, and Yan Zhang. "Characterization of santalene synthases using an inorganic pyrophosphatase coupled colorimetric assay." Analytical Biochemistry 547 (April 2018): 26–36. http://dx.doi.org/10.1016/j.ab.2018.02.002.
Full textMuñoz, Orlando, Phlippe Christen, Silvian Cretton, Alejandro F. Barrero, Armando Lara, and 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, no. 6 (June 2011): 1934578X1100600. http://dx.doi.org/10.1177/1934578x1100600630.
Full textVerdan, Maria Helena, Carlos Augusto Ehrenfried, Dilamara Riva Scharf, Armando Carlos Cervi, Marcos José Salvador, Andersson Barison, and Maria Elida A. Stefanello. "Chemical Constituents from Sinningia canescens and S. warmingii." Natural Product Communications 9, no. 10 (October 2014): 1934578X1400901. http://dx.doi.org/10.1177/1934578x1400901033.
Full textJia, Dan, Shuo Xu, Jie Sun, Chuanbo Zhang, Dashuai Li, and Wenyu Lu. "Yarrowia lipolytica construction for heterologous synthesis of α-santalene and fermentation optimization." Applied Microbiology and Biotechnology 103, no. 8 (March 12, 2019): 3511–20. http://dx.doi.org/10.1007/s00253-019-09735-w.
Full textWeston, Roderick J., and Gerald J. Smith. "Sesquiterpenes from the Inner Bark of the Silver Birch and the Paper Birch." Natural Product Communications 7, no. 2 (February 2012): 1934578X1200700. http://dx.doi.org/10.1177/1934578x1200700202.
Full textUNNIKRISHNAN, P. A. "ChemInform Abstract: A Highly Stereoselective Transformation of β-Santalene into (E)-. beta.-Santalol." ChemInform 26, no. 5 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199505224.
Full textTippmann, Stefan, Gionata Scalcinati, Verena Siewers, and Jens Nielsen. "Production of farnesene and santalene bySaccharomyces cerevisiaeusing fed-batch cultivations withRQ-controlled feed." Biotechnology and Bioengineering 113, no. 1 (September 2, 2015): 72–81. http://dx.doi.org/10.1002/bit.25683.
Full textThang, Tran D., Do N. Dai, Tran M. Hoi, and Isiaka A. Ogunwande. "Essential Oils from Five Species of Annonaceae from Vietnam." Natural Product Communications 8, no. 2 (February 2013): 1934578X1300800. http://dx.doi.org/10.1177/1934578x1300800228.
Full textAryal, Hari Prasad, and Usha Budathoki. "Systematics of Nepalese Termitomyces." Our Nature 13, no. 1 (December 27, 2015): 31–44. http://dx.doi.org/10.3126/on.v13i1.14207.
Full textJindal, Garima, and Raghavan B. Sunoj. "Revisiting sesquiterpene biosynthetic pathways leading to santalene and its analogues: a comprehensive mechanistic study." Organic & Biomolecular Chemistry 10, no. 39 (2012): 7996. http://dx.doi.org/10.1039/c2ob26027a.
Full textKloster, Adriana C., and Silvia C. Gnaedinger. "Coniferous wood of Agathoxylon from the La Matilde Formation, (Middle Jurassic), Santa Cruz, Argentina." Journal of Paleontology 92, no. 4 (April 2, 2018): 546–67. http://dx.doi.org/10.1017/jpa.2017.145.
Full textDi Girolamo, Alice, Janani Durairaj, Adèle van Houwelingen, Francel Verstappen, Dirk Bosch, Katarina Cankar, Harro Bouwmeester, Dick de Ridder, Aalt D. J. van Dijk, and Jules Beekwilder. "The santalene synthase from Cinnamomum camphora: Reconstruction of a sesquiterpene synthase from a monoterpene synthase." Archives of Biochemistry and Biophysics 695 (November 2020): 108647. http://dx.doi.org/10.1016/j.abb.2020.108647.
Full textMordini, Alessandro, Sabina Pecchi, and Giuseppe Capozzi. "The synthesis of 4′-thia-α-santalene and 4′-thia-α-santalol through an organometallic approach." Tetrahedron 50, no. 20 (January 1994): 6029–36. http://dx.doi.org/10.1016/s0040-4020(01)90455-7.
Full textKrotz, Achim, and Günter Helmchen. "Total syntheses of sandalwood fragrances: (Z)- and (E)-β-santalol and their enantiomers, ent-β-santalene." Tetrahedron: Asymmetry 1, no. 8 (January 1990): 537–40. http://dx.doi.org/10.1016/s0957-4166(00)80544-3.
Full textOppolzer, Wolfgang, Christian Chapuis, Dominique Dupuis, and Maodao Guo. "AsymmetricDiels-Alder Reactions of Neopentyl-Ether-Shielded Acrylates and Allenic Esters: Syntheses of (?)-Norbornenone and (?)-?-Santalene." Helvetica Chimica Acta 68, no. 8 (December 18, 1985): 2100–2114. http://dx.doi.org/10.1002/hlca.19850680803.
Full textZhong, Guo-fu, and Manfred Schlosser. "4′-Oxa-α-santalene and 4′-oxa-α-santalol : An olfactory comparison with the analogous natural sesquiterpenes." Tetrahedron Letters 34, no. 39 (September 1993): 6265–68. http://dx.doi.org/10.1016/s0040-4039(00)73727-0.
Full textScalcinati, Gionata, Siavash Partow, Verena Siewers, Michel Schalk, Laurent Daviet, and Jens Nielsen. "Combined metabolic engineering of precursor and co-factor supply to increase α-santalene production by Saccharomyces cerevisiae." Microbial Cell Factories 11, no. 1 (2012): 117. http://dx.doi.org/10.1186/1475-2859-11-117.
Full textZhong, Guo-fu, and Manfred Schlosser. "A Short and Simple Access to Both Enantiomers of Epi-β-santalene and (Z)-Epi-β-santalol." Synlett 1994, no. 03 (1994): 173–74. http://dx.doi.org/10.1055/s-1994-22781.
Full textKamikubo, Takashi, and 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, no. 2 (February 1995): 95–96. http://dx.doi.org/10.1246/cl.1995.95.
Full textMORDINI, A., S. PECCHI, and G. CAPOZZI. "ChemInform Abstract: Synthesis of 4′-Thia-α-santalene and 4′-Thia-α-santalol Through an Organometallic Approach." ChemInform 25, no. 39 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199439232.
Full textCoulerie, Paul, Louis Thouvenot, Mohammed Nour, and Yoshinori Asakawa. "Chemical Originalities of New Caledonian Liverworts from Lejeuneaceae Family." Natural Product Communications 10, no. 9 (September 2015): 1934578X1501000. http://dx.doi.org/10.1177/1934578x1501000903.
Full textZHONG, G. F., and M. SCHLOSSER. "ChemInform Abstract: A Short and Simple Access to Both Enantiomers of Epi-β-santalene and (Z)-Epi-β-santalol." ChemInform 25, no. 34 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199434206.
Full textKAMIKUBO, T., and 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, no. 29 (August 17, 2010): no. http://dx.doi.org/10.1002/chin.199529250.
Full textBaldovini, Nicolas, and 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, no. 8 (May 2002): 885–89. http://dx.doi.org/10.1016/s0957-4166(02)00194-5.
Full textJones, Christopher G., Jessie Moniodis, Katherine G. Zulak, Adrian Scaffidi, Julie A. Plummer, Emilio L. Ghisalberti, Elizabeth L. Barbour, and 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, no. 45 (November 2, 2012): 37713–14. http://dx.doi.org/10.1074/jbc.a111.231787.
Full textJones, Christopher G., Jessie Moniodis, Katherine G. Zulak, Adrian Scaffidi, Julie A. Plummer, Emilio L. Ghisalberti, Elizabeth L. Barbour, and 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, no. 20 (March 24, 2011): 17445–54. http://dx.doi.org/10.1074/jbc.m111.231787.
Full textBarton, Dustin, and 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, no. 3 (March 24, 2021): 939–52. http://dx.doi.org/10.1007/s11224-021-01764-4.
Full textKrotz, Achim, and 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, no. 6 (June 13, 1994): 601–9. http://dx.doi.org/10.1002/jlac.199419940610.
Full textMuturi, Ephantus J., William T. Hay, Kenneth M. Doll, Jose L. Ramirez, and Gordon Selling. "Insecticidal Activity of Commiphora erythraea Essential Oil and Its Emulsions Against Larvae of Three Mosquito Species." Journal of Medical Entomology 57, no. 6 (May 30, 2020): 1835–42. http://dx.doi.org/10.1093/jme/tjaa097.
Full textChen, Yanhang, Musavvara Kh Shukurova, Yonathan Asikin, Miyako Kusano, and Kazuo N. Watanabe. "Characterization of Volatile Organic Compounds in Mango Ginger (Curcuma amada Roxb.) from Myanmar." Metabolites 11, no. 1 (December 30, 2020): 21. http://dx.doi.org/10.3390/metabo11010021.
Full textRoussis, Vassilios, Constantinos Vagias, Christina Tsitsimpikou, and Nina Diamantopoulou. "Chemical Variability of the Volatile Metabolites from the Caribbean Corals of the Genus Gorgonia." Zeitschrift für Naturforschung C 55, no. 5-6 (June 1, 2000): 431–41. http://dx.doi.org/10.1515/znc-2000-5-620.
Full textScalcinati, Gionata, Christoph Knuf, Siavash Partow, Yun Chen, Jérôme Maury, Michel Schalk, Laurent Daviet, Jens Nielsen, and 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, no. 2 (March 2012): 91–103. http://dx.doi.org/10.1016/j.ymben.2012.01.007.
Full textKROTZ, A., and 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, no. 45 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199445192.
Full textJuvik, John A. "IMPROVED HOST PLANT RESISTANCE BY MODIFICATION OF PLANT CHEMICAL CUES ASSOCIATED WITH HELIOTHIS ZEA HOST PLANT SELECTION FOR OVIPOSITION." HortScience 25, no. 9 (September 1990): 1178a—1178. http://dx.doi.org/10.21273/hortsci.25.9.1178a.
Full textTanase, Corneliu, Ruxandra Ștefănescu, Béla Darkó, Daniela Lucia Muntean, Anca Corina Fărcaş, and Sonia Ancuţa Socaci. "Biochemical and Histo-Anatomical Responses of Lavandula angustifolia Mill. to Spruce and Beech Bark Extracts Application." Plants 9, no. 7 (July 7, 2020): 859. http://dx.doi.org/10.3390/plants9070859.
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