"Amination" 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.
The creation of an amine. It can be produced by the addition of an amino group to an organic compound or reduction of a nitro group.
| Descriptor ID |
D000586
|
| MeSH Number(s) |
G02.111.053 G02.607.110 G03.068
|
| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Amination".
Below are MeSH descriptors whose meaning is more specific than "Amination".
This graph shows the total number of publications written about "Amination" by people in this website by year, and whether "Amination" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2001 | 0 | 1 | 1 |
| 2003 | 0 | 1 | 1 |
| 2004 | 0 | 1 | 1 |
| 2008 | 0 | 1 | 1 |
| 2013 | 0 | 1 | 1 |
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Below are the most recent publications written about "Amination" by people in Profiles.
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Shen L, Maddox MM, Adhikari S, Bruhn DF, Kumar M, Lee RE, Hurdle JG, Lee RE, Sun D. Syntheses and evaluation of macrocyclic engelhardione analogs as antitubercular and antibacterial agents. J Antibiot (Tokyo). 2013 Jun; 66(6):319-25.
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Shukla MK, Leszczynski J. Hydration-dependent structural deformation of guanine in the electronic singlet excited state. J Phys Chem B. 2008 Apr 24; 112(16):5139-52.
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Gunda P, Russon LM, Lakshman MK. Pd-catalyzed amination of nucleoside arylsulfonates to yield N6-aryl-2,6-diaminopurine nucleosides. Angew Chem Int Ed Engl. 2004 Nov 26; 43(46):6372-7.
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Lakshman MK, Gunda P. Palladium-catalyzed synthesis of carcinogenic polycyclic aromatic hydrocarbon epoxide-nucleoside adducts: the first amination of a chloro nucleoside. Org Lett. 2003 Jan 09; 5(1):39-42.
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Zhao H, Hans S, Cheng X, Mootoo DR. Allylated monosaccharides as precursors in triple reductive amination strategies: synthesis of castanospermine and swainsonine. J Org Chem. 2001 Mar 09; 66(5):1761-7.