Academic literature on the topic 'Santalenes'

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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.

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Cheng, 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.

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Arai, 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.

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Daramwar, 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.

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Ngo, 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.

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Fifteen compounds (2 – 11) have been isolated from the spontaneous slow autoxidation of the tri-substituted double bond in the side-chain of the tricyclic sesquiterpene α-santalene; most of these compounds have also been reported as natural products.
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Unnikrishnan, 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.

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UNNIKRISHNAN, 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.

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Takano, 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.

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Guo, 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.

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To develop natural product resources from the Clausena genus (Rutaceae), the essential oils (EOs) from four Clausena plants (Clausena excavata, C. lansium, C. emarginata, and C. dunniana) were analyzed by GC-MS. Their lethal (contact toxicity) and sublethal effects (repellency) against Liposcelis bostrychophila (LB) adults were also evaluated. Santalene sesquiterpene was the precursor substance of santalol, a valuable perfumery. It was found that plenty of α-santalol (31.7%) and α-santalane (19.5%) contained in C. lansium from Guangxi Province and α-santalene (1.5%) existed in C. emarginata. Contact toxicity of the four EOs was observed, especially C. dunniana (LD50 = 37.26 µg/cm2). Santalol (LD50 = 30.26 µg/cm2) and estragole (LD50 = 30.22 µg/cm2) were the two most toxic compounds. In repellency assays, C. excavate, C. lansium, and C. emarginata exhibited repellent effect at the dose of 63.17 nL/cm2 2 h after exposure (percentage repellencies were 100%, 98%, and 96%, respectively). Four Clausena EOs and santalol had an excellent potential for application in the management of LB. Clausena plants could be further developed to find more resources of natural products.
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Kelsey, 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.

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The bark and leaf essential oil of Umbellularia californica (Hook. & Arn.) Nutt. from west central Oregon, USA, was isolated by steam distillation and the chemical composition analyzed by GC-FID and GC-MS. The three major components in bark oil were 1,8-cineole (36.0%), α-santalene (9.3), and α-terpineol (6.9%), while those in leaf oil were umbellulone (41.0%), 1,8-cineole (22.0%) and sabinene (10.2%).
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Dissertations / Theses on the topic "Santalenes"

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Jones, Christopher G. "The best of Santalum album : essential oil composition, biosynthesis and genetic diversity in the Australian tropical sandalwood collection." University of Western Australia. School of Plant Biology, 2008. http://theses.library.uwa.edu.au/adt-WU2008.0146.

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[Truncated abstract] An investigation into the causes of heartwood and essential oil content of Australian plantation sandalwood, Santalum album was undertaken. Genetic diversity of 233 S. album, five S. austrocaledonicum and fifteen S. macgregorii trees growing in the Forest Products Commission arboretum, Kununurra WA, was assessed using nuclear and chloroplast RFLPs. Santalum spicatum was chosen as an out-group. Nuclear genetic diversity of the S. album collection was very low, with observed and expected heterozygosity levels of 0.047. This was lower than the results previously reported in the literature for trees in India, however a different technique was used. Based on allelic patterns, the collection was able to be categorised into 19 genotypes; each representing some shared genetic origin. Some groups were highly redundant with 56 trees being represented, while others were populated by just one tree. The essential oil yield and heartwood contents of trees from these genetic groups were compared. Yields were highly variable both within and between groups of trees which share a common genetic history, suggesting a significant environmental component was contributing to the observed phenotype, despite identical soil and climatic conditions. Ancestral lineages were tested using chloroplast RFLPs, although a lack of shared mutations between species made this difficult. Only one S. album tree originating from Timor was resolved using nuclear RFLPs, with the other trees being grouped with material sourced from India. There was no resolution of Indian S. album from Timorese using chloroplast RFLPs, however one S. album tree grown from Indian seed possessed a single unique mutation. The low genetic diversity of the Australian S. album collection is likely to be a combination of incomplete seed sourcing and highly restricted gene flow during the evolution of the species. Combined with information gathered on the phylogeny of the genus by other researchers, S. album is postulated to have originated from an over-sea dispersal out of northern Australia or Papua New Guinea 3 to 5 million years ago. Essential oil yield and composition was assessed for 100 S. album trees growing in the collection, ranging in age from 8 to 17 years. Oil content of heartwood ranged from 30 mg g-1 to 60 mg g-1, and the transition zone 36 mg g-1 to 90 mg g-1. Sapwood contained almost no sesquiterpene oils. Despite the highly variable total oil yields, the chemical profile of the oil did not vary, suggesting there was limited genetic diversity within this region of the genome. Strong, positive correlations existed between v sesquiterpenoids in the essential oil of S. album. ... These represent the first TPS genes to be isolated from sandalwood and will enable further elucidation of oil biosynthesis genes. This thesis compiles a three-pronged approach to understanding the underlying causes of oil yield variation in S. album. As a species for which so little is known, the research presented here provides a major leap forward for tree improvement, breeding and silviculture. Hence the best of Santalum album research is presented.
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Book chapters on the topic "Santalenes"

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"12-Acetoxy-α-santalene." In Natural Compounds, 1137. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-0539-9_2175.

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