"Alkynes" 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.
Hydrocarbons with at least one triple bond in the linear portion, of the general formula Cn-H2n-2.
Descriptor ID |
D000480
|
MeSH Number(s) |
D02.455.326.397
|
Concept/Terms |
Alkynes- Alkynes
- Acetylenic Compounds
- Acetylenes
|
Below are MeSH descriptors whose meaning is more general than "Alkynes".
Below are MeSH descriptors whose meaning is more specific than "Alkynes".
This graph shows the total number of publications written about "Alkynes" by people in this website by year, and whether "Alkynes" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2002 | 0 | 2 | 2 |
2006 | 1 | 0 | 1 |
2008 | 1 | 0 | 1 |
2013 | 0 | 1 | 1 |
2014 | 2 | 0 | 2 |
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Below are the most recent publications written about "Alkynes" by people in Profiles.
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In Utero Efavirenz Exposure and Neurodevelopmental Outcomes in HIV-exposed Uninfected Children in Botswana. Pediatr Infect Dis J. 2019 08; 38(8):828-834.
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Regioselective synthesis of enones via a titanium-promoted coupling of unsymmetrical alkynes with weinreb amides. J Org Chem. 2014 Sep 05; 79(17):8469-76.
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Sterically directed iridium-catalyzed hydrosilylation of alkenes in the presence of alkynes. Org Lett. 2014 Mar 07; 16(5):1330-3.
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Dolutegravir, a second-generation integrase inhibitor for the treatment of HIV-1 infection. Ann Pharmacother. 2014 Mar; 48(3):395-403.
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Zinc-catalyzed silylation of terminal alkynes. J Org Chem. 2008 Apr 04; 73(7):2912-5.
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Efficient synthesis of N-methoxyindoles via alkylative cycloaddition of nitrosoarenes with alkynes. J Org Chem. 2006 Jan 20; 71(2):823-5.
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Symptomatic orthostasis with extended-release nifedipine and protease inhibitors. Pharmacotherapy. 2002 Oct; 22(10):1312-6.
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A novel and direct synthesis of indoles via catalytic reductive annulation of nitroaromatics with alkynes. Chem Commun (Camb). 2002 Mar 07; (5):484-5.