 Amines
"Amines" 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.
A group of compounds derived from ammonia by substituting organic radicals for the hydrogens. (From Grant & Hackh's Chemical Dictionary, 5th ed)
| Descriptor ID |
D000588
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| MeSH Number(s) |
D02.092
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Amines".
Below are MeSH descriptors whose meaning is more specific than "Amines".
This graph shows the total number of publications written about "Amines" by people in this website by year, and whether "Amines" 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 |
|---|
| 2000 | 0 | 1 | 1 | | 2008 | 0 | 1 | 1 | | 2009 | 1 | 0 | 1 | | 2010 | 0 | 1 | 1 | | 2011 | 0 | 1 | 1 | | 2013 | 1 | 2 | 3 |
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Below are the most recent publications written about "Amines" by people in Profiles.
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Hong CM, Statsyuk AV. The development of a one pot, regiocontrolled, three-component reaction for the synthesis of thieno[2,3-c]pyrroles. Org Biomol Chem. 2013 May 14; 11(18):2932-5.
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Lupulescu AI, Kumar M, Rimer JD. A facile strategy to design zeolite L crystals with tunable morphology and surface architecture. J Am Chem Soc. 2013 May 01; 135(17):6608-17.
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Besandre R, Jaimes M, May JA. Indoles synthesized from amines via copper catalysis. Org Lett. 2013 Apr 05; 15(7):1666-9.
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Napolitano R, Soesbe TC, De León-Rodríguez LM, Sherry AD, Udugamasooriya DG. On-bead combinatorial synthesis and imaging of chemical exchange saturation transfer magnetic resonance imaging agents to identify factors that influence water exchange. J Am Chem Soc. 2011 Aug 24; 133(33):13023-30.
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Kohler MC, Yost JM, Garnsey MR, Coltart DM. Direct carbon-carbon bond formation via soft enolization: a biomimetic asymmetric Mannich reaction of phenylacetate thioesters. Org Lett. 2010 Aug 06; 12(15):3376-9.
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Prasad BA, Gilbertson SR. One-pot synthesis of unsymmetrical N-heterocyclic carbene ligands from N-(2-iodoethyl)arylamine salts. Org Lett. 2009 Aug 20; 11(16):3710-3.
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Agarkov A, Gilbertson SR. Preparation of a library of unsymmetrical ureas based on 8-azabicyclo[3.2.1]octane scaffold. J Comb Chem. 2008 Sep-Oct; 10(5):655-7.
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Vincent F, Widger WR, Openshaw M, Gaskell SJ, Kohn H. 5a-formylbicyclomycin: studies on the bicyclomycin-Rho interaction. Biochemistry. 2000 Aug 08; 39(31):9067-76.
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Jandhyala BS, Vogin EE, Buckley JP. Evaluation and mechanism of action of two hypotensive substituted diamines. J Pharm Sci. 1965 May; 54(5):727-30.
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Brune GG. Biogenic amines in mental illness. Int Rev Neurobiol. 1965; 8:197-220.
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