Pinene (English Wikipedia)

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

refsWebsite

Global rank English rank

14doi.org

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8nih.gov

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4harvard.edu

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2dguv.de

813^th place

4,749^th place

1taylorfrancis.com

3,142^nd place

2,072^nd place

1ukm.my

low place

dguv.de

gestis.dguv.de

Record of alpha-Pinen in the GESTIS Substance Database of the Institute for Occupational Safety and Health, accessed on 07-January-2016.
Record of beta-Pinen in the GESTIS Substance Database of the Institute for Occupational Safety and Health, accessed on 07-January-2016.

doi.org

Gscheidmeier, Manfred; Fleig, Helmut (2000). "Turpentines". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a27_267. ISBN 3527306730.
Lincoln DE, Lawrence BM (1984). "The Volatile Constituents of Camphorweed, Heterotheca subaxillaris". Phytochemistry. 23 (4): 933–934. Bibcode:1984PChem..23..933L. doi:10.1016/S0031-9422(00)85073-6.
Sarria S, Wong B, Martín HG, Keasling JD, Peralta-Yahya P (2014). "Microbial Synthesis of Pinene". ACS Synthetic Biology. 3 (7): 466–475. doi:10.1021/sb4001382. PMID 24679043.
Nerio LS, Olivero-Verbel J, Stashenko E (2010). "Repellent activity of essential oils: a review". Bioresour Technol. 101 (1): 372–378. Bibcode:2010BiTec.101..372N. doi:10.1016/j.biortech.2009.07.048. PMID 19729299.
Russo EB (2011). "Taming THC: potential cannabis synergy and phytocannabinoid-terpenoid entourage effects". British Journal of Pharmacology. 163 (7): 1344–1364. doi:10.1111/j.1476-5381.2011.01238.x. PMC 3165946. PMID 21749363.
Köse EO, Deniz İG, Sarıkürkçü C, Aktaş Ö, Yavuz M (2010). "Chemical composition, antimicrobial and antioxidant activities of the essential oils of Sideritis erythrantha Boiss. and Heldr. (var. erythrantha and var. cedretorum P.H. Davis) endemic in Turkey". Food and Chemical Toxicology. 48 (10): 2960–2965. doi:10.1016/j.fct.2010.07.033. PMID 20670669.
Özek G, Demirci F, Özek T, Tabanca N, Wedge DE, Khan SI, et al. (2010). "Gas chromatographic-mass spectrometric analysis of volatiles obtained by four different techniques from Salvia rosifolia Sm., and evaluation for biological activity". Journal of Chromatography A. 1217 (5): 741–748. doi:10.1016/j.chroma.2009.11.086. PMID 20015509.
Hillig KW (2004). "A chemotaxonomic analysis of terpenoid variation in Cannabis". Biochemical Systematics and Ecology. 32 (10): 875–891. Bibcode:2004BioSE..32..875H. doi:10.1016/j.bse.2004.04.004.
Neuenschwander U, Guignard F, Hermans I (2010). "Mechanism of the Aerobic Oxidation of α-Pinene". ChemSusChem (in German). 3 (1): 75–84. Bibcode:2010ChSCh...3...75N. doi:10.1002/cssc.200900228. PMID 20017184.
Mark R. Sivik, Kenetha J. Stanton, Leo A. Paquette (1995). "(1R,5R)-(+)-Verbenone of High Optical Purity". Organic Syntheses. 72: 57. doi:10.15227/orgsyn.072.0057.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Abbott, Jason; Allais, Christophe; Roush, William R. (2015). "Preparation of Crystalline (Diisopinocampheyl)borane". Organic Syntheses. 92: 26–37. doi:10.15227/orgsyn.092.0026.
Midland, M. Mark (15 April 2001). "B -3-Pinanyl-9-borabicyclo[3.3.1]nonane". Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rp173.
Charles A. Brown, Prabhakav K. Jadhav (1987). "(a)-b-PINENE BY ISOMERIZATION OF (B)-b-PINENE". Organic Syntheses. 65: 224. doi:10.15227/orgsyn.065.0224.
Raman V, Sivasankaralingam V, Dibble R, Sarathy SM (2016). "α-Pinene - A High Energy Density Biofuel for SI Engine Applications". SAE Technical Paper. SAE Technical Paper Series. 1. doi:10.4271/2016-01-2171.

harvard.edu

ui.adsabs.harvard.edu

Lincoln DE, Lawrence BM (1984). "The Volatile Constituents of Camphorweed, Heterotheca subaxillaris". Phytochemistry. 23 (4): 933–934. Bibcode:1984PChem..23..933L. doi:10.1016/S0031-9422(00)85073-6.
Nerio LS, Olivero-Verbel J, Stashenko E (2010). "Repellent activity of essential oils: a review". Bioresour Technol. 101 (1): 372–378. Bibcode:2010BiTec.101..372N. doi:10.1016/j.biortech.2009.07.048. PMID 19729299.
Hillig KW (2004). "A chemotaxonomic analysis of terpenoid variation in Cannabis". Biochemical Systematics and Ecology. 32 (10): 875–891. Bibcode:2004BioSE..32..875H. doi:10.1016/j.bse.2004.04.004.
Neuenschwander U, Guignard F, Hermans I (2010). "Mechanism of the Aerobic Oxidation of α-Pinene". ChemSusChem (in German). 3 (1): 75–84. Bibcode:2010ChSCh...3...75N. doi:10.1002/cssc.200900228. PMID 20017184.

nih.gov

pubmed.ncbi.nlm.nih.gov

Sarria S, Wong B, Martín HG, Keasling JD, Peralta-Yahya P (2014). "Microbial Synthesis of Pinene". ACS Synthetic Biology. 3 (7): 466–475. doi:10.1021/sb4001382. PMID 24679043.
Nerio LS, Olivero-Verbel J, Stashenko E (2010). "Repellent activity of essential oils: a review". Bioresour Technol. 101 (1): 372–378. Bibcode:2010BiTec.101..372N. doi:10.1016/j.biortech.2009.07.048. PMID 19729299.
Russo EB (2011). "Taming THC: potential cannabis synergy and phytocannabinoid-terpenoid entourage effects". British Journal of Pharmacology. 163 (7): 1344–1364. doi:10.1111/j.1476-5381.2011.01238.x. PMC 3165946. PMID 21749363.
Köse EO, Deniz İG, Sarıkürkçü C, Aktaş Ö, Yavuz M (2010). "Chemical composition, antimicrobial and antioxidant activities of the essential oils of Sideritis erythrantha Boiss. and Heldr. (var. erythrantha and var. cedretorum P.H. Davis) endemic in Turkey". Food and Chemical Toxicology. 48 (10): 2960–2965. doi:10.1016/j.fct.2010.07.033. PMID 20670669.
Özek G, Demirci F, Özek T, Tabanca N, Wedge DE, Khan SI, et al. (2010). "Gas chromatographic-mass spectrometric analysis of volatiles obtained by four different techniques from Salvia rosifolia Sm., and evaluation for biological activity". Journal of Chromatography A. 1217 (5): 741–748. doi:10.1016/j.chroma.2009.11.086. PMID 20015509.
Neuenschwander U, Guignard F, Hermans I (2010). "Mechanism of the Aerobic Oxidation of α-Pinene". ChemSusChem (in German). 3 (1): 75–84. Bibcode:2010ChSCh...3...75N. doi:10.1002/cssc.200900228. PMID 20017184.

ncbi.nlm.nih.gov

Russo EB (2011). "Taming THC: potential cannabis synergy and phytocannabinoid-terpenoid entourage effects". British Journal of Pharmacology. 163 (7): 1344–1364. doi:10.1111/j.1476-5381.2011.01238.x. PMC 3165946. PMID 21749363.

pubchem.ncbi.nlm.nih.gov

"alpha-Pinene - Compound Summary". PubChem. NCBI. Retrieved 14 Nov 2017.

taylorfrancis.com

Noma Y, Asakawa Y (2010). "Biotransformation of Monoterpenoids by Microorganisms, Insects, and Mammals". In Baser KH, Buchbauer G (eds.). Handbook of Essential Oils: Science, Technology, and Applications (2nd ed.). Boca Raton, FL: CRC Press. pp. 585–736. ISBN 9780429155666.

ukm.my

Kasuan N (2013). "Extraction of Citrus hystrix D.C. (Kaffir Lime) Essential Oil Using Automated Steam Distillation Process: Analysis of Volatile Compounds" (PDF). Malaysian Journal of Analytical Sciences. 17 (3): 359–369.