Terpene (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Terpene" in English language version.

refsWebsite

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29doi.org

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23nih.gov

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6semanticscholar.org

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4harvard.edu

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2books.google.com

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2nobelprize.org

301^st place

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2worldcat.org

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1rareterpenes.com

low place

1springer.com

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1iupac.org

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1figshare.com

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1deliverymeds.ca

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1theguardian.com

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1classicfm.com

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1ajevonline.org

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ajevonline.org

Winterhalter, P.; Sefton, M. A.; Williams, P. J. (1990). "Volatile C₁₃-Norisoprenoid Compounds in Riesling Wine Are Generated From Multiple Precursors". American Journal of Enology and Viticulture. 41 (4): 277–283. doi:10.5344/ajev.1990.41.4.277. S2CID 101007887.

books.google.com

Kekulé, August (1866). Lehrbuch der organischen Chemie [Textbook of Organic Chemistry] (in German). Vol. 2. Erlangen, (Germany): Ferdinand Enke. pp. 464–465. From pp. 464–465: "Mit dem Namen Terpene bezeichnen wir … unter verschiedenen Namen aufgeführt werden." (By the name "terpene" we designate in general the hydrocarbons composed according to the [empirical] formula C₁₀H₁₆ (see §. 1540)
Breitmaier, Eberhard (2006). Terpenes: Flavors, Fragrances, Pharmaca, Pheromones. John Wiley & Sons. pp. 1–13. ISBN 978-3527317868.

classicfm.com

Roberts, Maddy Shaw (22 January 2019). "What the heck is rosin – and why do violinists need it?". Classic FM. Retrieved 22 July 2022.

deliverymeds.ca

"An Introduction to Terpenes".

doi.org

Eberhard Breitmaier (2006). Terpenes: Flavors, Fragrances, Pharmaca, Pheromones. Wiley-VCH. doi:10.1002/9783527609949. ISBN 9783527609949.
Davis, Edward M.; Croteau, Rodney (2000). "Cyclization enzymes in the biosynthesis of monoterpenes, sesquiterpenes, and diterpenes". Biosynthesis. Vol. 209. pp. 53–95. doi:10.1007/3-540-48146-X_2. ISBN 978-3-540-66573-1. {{cite book}}: |journal= ignored (help)
Eggersdorfer, Manfred. "Terpenes". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a26_205. ISBN 978-3527306732.
"IUPAC Gold Book - terpenoids". doi:10.1351/goldbook.T06279. {{cite journal}}: Cite journal requires |journal= (help)
Chen, Ke; Baran, Phil S. (June 2009). "Total synthesis of eudesmane terpenes by site-selective C–H oxidations". Nature. 459 (7248): 824–828. Bibcode:2009Natur.459..824C. doi:10.1038/nature08043. PMID 19440196. S2CID 4312428.
Hillier, Stephen G.; Lathe, Richard (2019). "Terpenes, hormones and life: Isoprene rule revisited". Journal of Endocrinology. 242 (2): R9–R22. doi:10.1530/JOE-19-0084. PMID 31051473.
Omar, Jone; Olivares, Maitane; Alonso, Ibone; Vallejo, Asier; Aizpurua-Olaizola, Oier; Etxebarria, Nestor (April 2016). "Quantitative Analysis of Bioactive Compounds from Aromatic Plants by Means of Dynamic Headspace Extraction and Multiple Headspace Extraction-Gas Chromatography-Mass Spectrometry: Quantitative analysis of bioactive compounds…". Journal of Food Science. 81 (4): C867–C873. doi:10.1111/1750-3841.13257. PMID 26925555. S2CID 21443154.
Martin, D. M.; Gershenzon, J.; Bohlmann, J. (July 2003). "Induction of Volatile Terpene Biosynthesis and Diurnal Emission by Methyl Jasmonate in Foliage of Norway Spruce". Plant Physiology. 132 (3): 1586–1599. doi:10.1104/pp.103.021196. PMC 167096. PMID 12857838.
Pichersky, E. (10 February 2006). "Biosynthesis of Plant Volatiles: Nature's Diversity and Ingenuity". Science. 311 (5762): 808–811. Bibcode:2006Sci...311..808P. doi:10.1126/science.1118510. PMC 2861909. PMID 16469917.
Roberts, Susan C (2007). "Production and engineering of terpenoids in plant cell culture". Nature Chemical Biology. 3 (7): 387–395. doi:10.1038/nchembio.2007.8. ISSN 1552-4450. PMID 17576426.
Nutting, W. L.; Blum, M. S.; Fales, H. M. (1974). "Behavior of the North American Termite, Tenuirostritermes tenuirostris, with Special Reference to the Soldier Frontal Gland Secretion, Its Chemical Composition, and Use in Defense". Psyche. 81 (1): 167–177. doi:10.1155/1974/13854.
Silvestre, Armando J.D.; Gandini, Alessandro (2008). "Terpenes: Major Sources, Properties and Applications". Monomers, Polymers and Composites from Renewable Resources. pp. 17–38. doi:10.1016/B978-0-08-045316-3.00002-8. ISBN 9780080453163.
Steenackers, B.; De Cooman, L.; De Vos, D. (2015). "Chemical transformations of characteristic hop secondary metabolites in relation to beer properties and the brewing process: A review". Food Chemistry. 172: 742–756. doi:10.1016/j.foodchem.2014.09.139. PMID 25442616.
Koziol, Agata; Stryjewska, Agnieszka; Librowski, Tadeusz; Salat, Kinga; Gawel, Magdalena; Moniczewski, Andrzej; Lochynski, Stanislaw (2014). "An Overview of the Pharmacological Properties and Potential Applications of Natural Monoterpenes". Mini-Reviews in Medicinal Chemistry. 14 (14): 1156–1168. doi:10.2174/1389557514666141127145820. PMID 25429661.
Koyama, Sachiko; Heinbockel, Thomas (2020). "The Effects of Essential Oils and Terpenes in Relation to Their Routes of Intake and Application". International Journal of Molecular Sciences. 21 (5): 1558. doi:10.3390/ijms21051558. PMC 7084246. PMID 32106479.
Isman, M. B. (2000). "Plant essential oils for pest and disease management". Crop Protection. 21 (8–10): 603–608. doi:10.1016/S0261-2194(00)00079-X. S2CID 39469817.
Ruzicka, L. (1953). "The isoprene rule and the biogenesis of terpenic compounds". Experientia. 9 (10): 357–367. doi:10.1007/BF02167631. PMID 13116962. S2CID 44195550.
Eschenmoser, Albert; Arigoni, Duilio (December 2005). "Revisited after 50 Years: The 'Stereochemical Interpretation of the Biogenetic Isoprene Rule for the Triterpenes'". Helvetica Chimica Acta. 88 (12): 3011–3050. doi:10.1002/hlca.200590245.
Hayakawa, Hajime; Motoyama, Kento; Sobue, Fumiaki; Ito, Tomokazu; Kawaide, Hiroshi; Yoshimura, Tohru; Hemmi, Hisashi (2018-10-02). "Modified mevalonate pathway of the archaeon Aeropyrum pernix proceeds via trans -anhydromevalonate 5-phosphate". Proceedings of the National Academy of Sciences. 115 (40): 10034–10039. Bibcode:2018PNAS..11510034H. doi:10.1073/pnas.1809154115. ISSN 0027-8424. PMC 6176645. PMID 30224495.
Kumari, I.; Ahmed, M.; Akhter, Y. (2017). "Evolution of catalytic microenvironment governs substrate and product diversity in trichodiene synthase and other terpene fold enzymes". Biochimie. 144: 9–20. doi:10.1016/j.biochi.2017.10.003. PMID 29017925.
Pazouki, L.; Niinemets, Ü. (2016). "Multi-Substrate Terpene Synthases: Their Occurrence and Physiological Significance". Frontiers in Plant Science. 7: 1019. doi:10.3389/fpls.2016.01019. PMC 4940680. PMID 27462341.
Boutanaev, A. M.; Moses, T.; Zi, J.; Nelson, D. R.; Mugford, S. T.; Peters, R. J.; Osbourn, A. (2015). "Investigation of terpene diversification across multiple sequenced plant genomes". Proceedings of the National Academy of Sciences. 112 (1): E81–E88. Bibcode:2015PNAS..112E..81B. doi:10.1073/pnas.1419547112. PMC 4291660. PMID 25502595.
Ružička, Leopold (1953). "The isoprene rule and the Biogenesis of terpenic compounds". Cellular and Molecular Life Sciences. 9 (10): 357–367. doi:10.1007/BF02167631. PMID 13116962. S2CID 44195550.
Ludwiczuk, A.; Skalicka-Woźniak, K.; Georgiev, M.I. (2017). "Terpenoids". Pharmacognosy: 233–266. doi:10.1016/B978-0-12-802104-0.00011-1. ISBN 9780128021040.
Günata, Z.; Wirth, J. L.; Guo, W.; Baumes, R. L. (2001). Carotenoid-Derived Aroma Compounds; chapter 13: Norisoprenoid Aglycon Composition of Leaves and Grape Berries from Muscat of Alexandria and Shiraz Cultivars. ACS Symposium Series. Vol. 802. pp. 255–261. doi:10.1021/bk-2002-0802.ch018. ISBN 978-0-8412-3729-2.
Winterhalter, P.; Sefton, M. A.; Williams, P. J. (1990). "Volatile C₁₃-Norisoprenoid Compounds in Riesling Wine Are Generated From Multiple Precursors". American Journal of Enology and Viticulture. 41 (4): 277–283. doi:10.5344/ajev.1990.41.4.277. S2CID 101007887.
Vinholes, J.; Coimbra, M. A.; Rocha, S. M. (2009). "Rapid tool for assessment of C₁₃ norisoprenoids in wines". Journal of Chromatography A. 1216 (47): 8398–8403. doi:10.1016/j.chroma.2009.09.061. PMID 19828152.
Zelena, K.; Hardebusch, B.; Hülsdau, B.; Berger, R. G.; Zorn, H. (2009). "Generation of Norisoprenoid Flavors from Carotenoids by Fungal Peroxidases". Journal of Agricultural and Food Chemistry. 57 (21): 9951–9955. doi:10.1021/jf901438m. PMID 19817422.
Cabaroğlu, T.; Selli, S.; Canbaş, A.; Lepoutre, J.-P.; Günata, Z. (2003). "Wine flavor enhancement through the use of exogenous fungal glycosidases". Enzyme and Microbial Technology. 33 (5): 581–587. doi:10.1016/S0141-0229(03)00179-0.

figshare.com

Omar, Jone; Olivares, Maitane; Alonso, Ibone; Vallejo, Asier; Aizpurua-Olaizola, Oier; Etxebarria, Nestor (April 2016). "Quantitative Analysis of Bioactive Compounds from Aromatic Plants by Means of Dynamic Headspace Extraction and Multiple Headspace Extraction-Gas Chromatography-Mass Spectrometry: Quantitative analysis of bioactive compounds…". Journal of Food Science. 81 (4): C867–C873. doi:10.1111/1750-3841.13257. PMID 26925555. S2CID 21443154.

harvard.edu

ui.adsabs.harvard.edu

Chen, Ke; Baran, Phil S. (June 2009). "Total synthesis of eudesmane terpenes by site-selective C–H oxidations". Nature. 459 (7248): 824–828. Bibcode:2009Natur.459..824C. doi:10.1038/nature08043. PMID 19440196. S2CID 4312428.
Pichersky, E. (10 February 2006). "Biosynthesis of Plant Volatiles: Nature's Diversity and Ingenuity". Science. 311 (5762): 808–811. Bibcode:2006Sci...311..808P. doi:10.1126/science.1118510. PMC 2861909. PMID 16469917.
Hayakawa, Hajime; Motoyama, Kento; Sobue, Fumiaki; Ito, Tomokazu; Kawaide, Hiroshi; Yoshimura, Tohru; Hemmi, Hisashi (2018-10-02). "Modified mevalonate pathway of the archaeon Aeropyrum pernix proceeds via trans -anhydromevalonate 5-phosphate". Proceedings of the National Academy of Sciences. 115 (40): 10034–10039. Bibcode:2018PNAS..11510034H. doi:10.1073/pnas.1809154115. ISSN 0027-8424. PMC 6176645. PMID 30224495.
Boutanaev, A. M.; Moses, T.; Zi, J.; Nelson, D. R.; Mugford, S. T.; Peters, R. J.; Osbourn, A. (2015). "Investigation of terpene diversification across multiple sequenced plant genomes". Proceedings of the National Academy of Sciences. 112 (1): E81–E88. Bibcode:2015PNAS..112E..81B. doi:10.1073/pnas.1419547112. PMC 4291660. PMID 25502595.

iupac.org

goldbook.iupac.org

"IUPAC Gold Book - terpenoids". doi:10.1351/goldbook.T06279. {{cite journal}}: Cite journal requires |journal= (help)

nih.gov

pubmed.ncbi.nlm.nih.gov

Chen, Ke; Baran, Phil S. (June 2009). "Total synthesis of eudesmane terpenes by site-selective C–H oxidations". Nature. 459 (7248): 824–828. Bibcode:2009Natur.459..824C. doi:10.1038/nature08043. PMID 19440196. S2CID 4312428.
Hillier, Stephen G.; Lathe, Richard (2019). "Terpenes, hormones and life: Isoprene rule revisited". Journal of Endocrinology. 242 (2): R9–R22. doi:10.1530/JOE-19-0084. PMID 31051473.
Omar, Jone; Olivares, Maitane; Alonso, Ibone; Vallejo, Asier; Aizpurua-Olaizola, Oier; Etxebarria, Nestor (April 2016). "Quantitative Analysis of Bioactive Compounds from Aromatic Plants by Means of Dynamic Headspace Extraction and Multiple Headspace Extraction-Gas Chromatography-Mass Spectrometry: Quantitative analysis of bioactive compounds…". Journal of Food Science. 81 (4): C867–C873. doi:10.1111/1750-3841.13257. PMID 26925555. S2CID 21443154.
Martin, D. M.; Gershenzon, J.; Bohlmann, J. (July 2003). "Induction of Volatile Terpene Biosynthesis and Diurnal Emission by Methyl Jasmonate in Foliage of Norway Spruce". Plant Physiology. 132 (3): 1586–1599. doi:10.1104/pp.103.021196. PMC 167096. PMID 12857838.
Pichersky, E. (10 February 2006). "Biosynthesis of Plant Volatiles: Nature's Diversity and Ingenuity". Science. 311 (5762): 808–811. Bibcode:2006Sci...311..808P. doi:10.1126/science.1118510. PMC 2861909. PMID 16469917.
Roberts, Susan C (2007). "Production and engineering of terpenoids in plant cell culture". Nature Chemical Biology. 3 (7): 387–395. doi:10.1038/nchembio.2007.8. ISSN 1552-4450. PMID 17576426.
Steenackers, B.; De Cooman, L.; De Vos, D. (2015). "Chemical transformations of characteristic hop secondary metabolites in relation to beer properties and the brewing process: A review". Food Chemistry. 172: 742–756. doi:10.1016/j.foodchem.2014.09.139. PMID 25442616.
Koziol, Agata; Stryjewska, Agnieszka; Librowski, Tadeusz; Salat, Kinga; Gawel, Magdalena; Moniczewski, Andrzej; Lochynski, Stanislaw (2014). "An Overview of the Pharmacological Properties and Potential Applications of Natural Monoterpenes". Mini-Reviews in Medicinal Chemistry. 14 (14): 1156–1168. doi:10.2174/1389557514666141127145820. PMID 25429661.
Koyama, Sachiko; Heinbockel, Thomas (2020). "The Effects of Essential Oils and Terpenes in Relation to Their Routes of Intake and Application". International Journal of Molecular Sciences. 21 (5): 1558. doi:10.3390/ijms21051558. PMC 7084246. PMID 32106479.
Ruzicka, L. (1953). "The isoprene rule and the biogenesis of terpenic compounds". Experientia. 9 (10): 357–367. doi:10.1007/BF02167631. PMID 13116962. S2CID 44195550.
Hayakawa, Hajime; Motoyama, Kento; Sobue, Fumiaki; Ito, Tomokazu; Kawaide, Hiroshi; Yoshimura, Tohru; Hemmi, Hisashi (2018-10-02). "Modified mevalonate pathway of the archaeon Aeropyrum pernix proceeds via trans -anhydromevalonate 5-phosphate". Proceedings of the National Academy of Sciences. 115 (40): 10034–10039. Bibcode:2018PNAS..11510034H. doi:10.1073/pnas.1809154115. ISSN 0027-8424. PMC 6176645. PMID 30224495.
Kumari, I.; Ahmed, M.; Akhter, Y. (2017). "Evolution of catalytic microenvironment governs substrate and product diversity in trichodiene synthase and other terpene fold enzymes". Biochimie. 144: 9–20. doi:10.1016/j.biochi.2017.10.003. PMID 29017925.
Pazouki, L.; Niinemets, Ü. (2016). "Multi-Substrate Terpene Synthases: Their Occurrence and Physiological Significance". Frontiers in Plant Science. 7: 1019. doi:10.3389/fpls.2016.01019. PMC 4940680. PMID 27462341.
Boutanaev, A. M.; Moses, T.; Zi, J.; Nelson, D. R.; Mugford, S. T.; Peters, R. J.; Osbourn, A. (2015). "Investigation of terpene diversification across multiple sequenced plant genomes". Proceedings of the National Academy of Sciences. 112 (1): E81–E88. Bibcode:2015PNAS..112E..81B. doi:10.1073/pnas.1419547112. PMC 4291660. PMID 25502595.
Ružička, Leopold (1953). "The isoprene rule and the Biogenesis of terpenic compounds". Cellular and Molecular Life Sciences. 9 (10): 357–367. doi:10.1007/BF02167631. PMID 13116962. S2CID 44195550.
Vinholes, J.; Coimbra, M. A.; Rocha, S. M. (2009). "Rapid tool for assessment of C₁₃ norisoprenoids in wines". Journal of Chromatography A. 1216 (47): 8398–8403. doi:10.1016/j.chroma.2009.09.061. PMID 19828152.
Zelena, K.; Hardebusch, B.; Hülsdau, B.; Berger, R. G.; Zorn, H. (2009). "Generation of Norisoprenoid Flavors from Carotenoids by Fungal Peroxidases". Journal of Agricultural and Food Chemistry. 57 (21): 9951–9955. doi:10.1021/jf901438m. PMID 19817422.

ncbi.nlm.nih.gov

Martin, D. M.; Gershenzon, J.; Bohlmann, J. (July 2003). "Induction of Volatile Terpene Biosynthesis and Diurnal Emission by Methyl Jasmonate in Foliage of Norway Spruce". Plant Physiology. 132 (3): 1586–1599. doi:10.1104/pp.103.021196. PMC 167096. PMID 12857838.
Pichersky, E. (10 February 2006). "Biosynthesis of Plant Volatiles: Nature's Diversity and Ingenuity". Science. 311 (5762): 808–811. Bibcode:2006Sci...311..808P. doi:10.1126/science.1118510. PMC 2861909. PMID 16469917.
Koyama, Sachiko; Heinbockel, Thomas (2020). "The Effects of Essential Oils and Terpenes in Relation to Their Routes of Intake and Application". International Journal of Molecular Sciences. 21 (5): 1558. doi:10.3390/ijms21051558. PMC 7084246. PMID 32106479.
Hayakawa, Hajime; Motoyama, Kento; Sobue, Fumiaki; Ito, Tomokazu; Kawaide, Hiroshi; Yoshimura, Tohru; Hemmi, Hisashi (2018-10-02). "Modified mevalonate pathway of the archaeon Aeropyrum pernix proceeds via trans -anhydromevalonate 5-phosphate". Proceedings of the National Academy of Sciences. 115 (40): 10034–10039. Bibcode:2018PNAS..11510034H. doi:10.1073/pnas.1809154115. ISSN 0027-8424. PMC 6176645. PMID 30224495.
Pazouki, L.; Niinemets, Ü. (2016). "Multi-Substrate Terpene Synthases: Their Occurrence and Physiological Significance". Frontiers in Plant Science. 7: 1019. doi:10.3389/fpls.2016.01019. PMC 4940680. PMID 27462341.
Boutanaev, A. M.; Moses, T.; Zi, J.; Nelson, D. R.; Mugford, S. T.; Peters, R. J.; Osbourn, A. (2015). "Investigation of terpene diversification across multiple sequenced plant genomes". Proceedings of the National Academy of Sciences. 112 (1): E81–E88. Bibcode:2015PNAS..112E..81B. doi:10.1073/pnas.1419547112. PMC 4291660. PMID 25502595.

nobelprize.org

Grandin, Karl, ed. (1966). "Leopold Ružička". Nobel Lectures, Chemistry: 1922-1941. Amsterdam: Elsevier Publishing Company.
Now available from "Leopold Ružička Biography". nobelprize.org. Nobel Foundation. 1939. Retrieved 6 July 2017.
"The Nobel Prize in Chemistry 1939".

rareterpenes.com

"What are Terpenes". rareterpenes.com. 13 April 2021.

semanticscholar.org

api.semanticscholar.org

Chen, Ke; Baran, Phil S. (June 2009). "Total synthesis of eudesmane terpenes by site-selective C–H oxidations". Nature. 459 (7248): 824–828. Bibcode:2009Natur.459..824C. doi:10.1038/nature08043. PMID 19440196. S2CID 4312428.
Omar, Jone; Olivares, Maitane; Alonso, Ibone; Vallejo, Asier; Aizpurua-Olaizola, Oier; Etxebarria, Nestor (April 2016). "Quantitative Analysis of Bioactive Compounds from Aromatic Plants by Means of Dynamic Headspace Extraction and Multiple Headspace Extraction-Gas Chromatography-Mass Spectrometry: Quantitative analysis of bioactive compounds…". Journal of Food Science. 81 (4): C867–C873. doi:10.1111/1750-3841.13257. PMID 26925555. S2CID 21443154.
Isman, M. B. (2000). "Plant essential oils for pest and disease management". Crop Protection. 21 (8–10): 603–608. doi:10.1016/S0261-2194(00)00079-X. S2CID 39469817.
Ruzicka, L. (1953). "The isoprene rule and the biogenesis of terpenic compounds". Experientia. 9 (10): 357–367. doi:10.1007/BF02167631. PMID 13116962. S2CID 44195550.
Ružička, Leopold (1953). "The isoprene rule and the Biogenesis of terpenic compounds". Cellular and Molecular Life Sciences. 9 (10): 357–367. doi:10.1007/BF02167631. PMID 13116962. S2CID 44195550.
Winterhalter, P.; Sefton, M. A.; Williams, P. J. (1990). "Volatile C₁₃-Norisoprenoid Compounds in Riesling Wine Are Generated From Multiple Precursors". American Journal of Enology and Viticulture. 41 (4): 277–283. doi:10.5344/ajev.1990.41.4.277. S2CID 101007887.

springer.com

link.springer.com

Dev, Sukh (1989). "Chapter 8. Isoprenoids: 8.1. Terpenoids.". In Rowe, John W. (ed.). Natural Products of Woody Plants: Chemicals Extraneous to the Lignocellulosic Cell Wall. Berlin and Heidelberg, Germany: Springer-Verlag. pp. 691–807. ; see p. 691.

theguardian.com

Adam, David (October 31, 2008). "Scientists discover cloud-thickening chemicals in trees that could offer a new weapon in the fight against global warming". The Guardian.

worldcat.org

Roberts, Susan C (2007). "Production and engineering of terpenoids in plant cell culture". Nature Chemical Biology. 3 (7): 387–395. doi:10.1038/nchembio.2007.8. ISSN 1552-4450. PMID 17576426.
Hayakawa, Hajime; Motoyama, Kento; Sobue, Fumiaki; Ito, Tomokazu; Kawaide, Hiroshi; Yoshimura, Tohru; Hemmi, Hisashi (2018-10-02). "Modified mevalonate pathway of the archaeon Aeropyrum pernix proceeds via trans -anhydromevalonate 5-phosphate". Proceedings of the National Academy of Sciences. 115 (40): 10034–10039. Bibcode:2018PNAS..11510034H. doi:10.1073/pnas.1809154115. ISSN 0027-8424. PMC 6176645. PMID 30224495.