 Alkenes
"Alkenes" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Unsaturated hydrocarbons of the type Cn-H2n, indicated by the suffix -ene. (Grant & Hackh's Chemical Dictionary, 5th ed, p408)
| Descriptor ID |
D000475
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| MeSH Number(s) |
D02.455.326.271
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Alkenes".
Below are MeSH descriptors whose meaning is more specific than "Alkenes".
This graph shows the total number of publications written about "Alkenes" by people in this website by year, and whether "Alkenes" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2001 | 0 | 1 | 1 | | 2004 | 1 | 0 | 1 | | 2005 | 0 | 1 | 1 | | 2009 | 3 | 0 | 3 | | 2010 | 1 | 0 | 1 | | 2012 | 1 | 0 | 1 | | 2013 | 1 | 0 | 1 | | 2015 | 0 | 1 | 1 | | 2020 | 1 | 0 | 1 | | 2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Alkenes" by people in Profiles.
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Aghaeinejad-Meybodi A, Mousavi SM, Shahabi AA, Kakroudi MR. CFD Modeling of Methanol to Light Olefins in a Sodalite Membrane Reactor using SAPO-34 Catalyst with In Situ Steam Removal. Comb Chem High Throughput Screen. 2021; 24(4):559-569.
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Deming BL, Ziemann PJ. Quantification of alkenes on indoor surfaces and implications for chemical sources and sinks. Indoor Air. 2020 09; 30(5):914-924.
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Bedford NM, Ramezani-Dakhel H, Slocik JM, Briggs BD, Ren Y, Frenkel AI, Petkov V, Heinz H, Naik RR, Knecht MR. Elucidation of peptide-directed palladium surface structure for biologically tunable nanocatalysts. ACS Nano. 2015 May 26; 9(5):5082-92.
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Barczak NT, Rooke DA, Menard ZA, Ferreira EM. Stereoselective synthesis of tetrasubstituted olefins through a halogen-induced 1,2-silyl migration. Angew Chem Int Ed Engl. 2013 Jul 15; 52(29):7579-82.
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Rooke DA, Ferreira EM. Palladium-catalyzed Hiyama couplings of a-silylenoates and a-silylenamides. Org Lett. 2012 Jul 06; 14(13):3328-31.
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Bouwman J, Goulay F, Leone SR, Wilson KR. Bimolecular rate constant and product branching ratio measurements for the reaction of C2H with ethene and propene at 79 K. J Phys Chem A. 2012 Apr 19; 116(15):3907-17.
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Trevitt AJ, Soorkia S, Savee JD, Selby TS, Osborn DL, Taatjes CA, Leone SR. Branching fractions of the CN + C3H6 reaction using synchrotron photoionization mass spectrometry: evidence for the 3-cyanopropene product. J Phys Chem A. 2011 Nov 24; 115(46):13467-73.
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Michl J. Photochemical CO2 reduction: towards an artificial leaf? Nat Chem. 2011 Apr; 3(4):268-9.
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Rooke DA, Ferreira EM. Stereoselective syntheses of trisubstituted olefins via platinum catalysis: alpha-silylenones with geometrical complementarity. J Am Chem Soc. 2010 Sep 01; 132(34):11926-8.
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Matsunaga A, Ziemann PJ. Yields of beta-hydroxynitrates, dihydroxynitrates, and trihydroxynitrates formed from OH radical-initiated reactions of 2-methyl-1-alkenes. Proc Natl Acad Sci U S A. 2010 Apr 13; 107(15):6664-9.
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