 Esters
"Esters" 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.
No definition found.
| Descriptor ID |
D004952
|
| MeSH Number(s) |
D02.241.400
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Esters".
Below are MeSH descriptors whose meaning is more specific than "Esters".
This graph shows the total number of publications written about "Esters" by people in this website by year, and whether "Esters" 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 |
|---|
| 2007 | 0 | 1 | 1 | | 2008 | 2 | 1 | 3 | | 2010 | 2 | 1 | 3 | | 2011 | 0 | 1 | 1 | | 2012 | 1 | 0 | 1 | | 2017 | 0 | 1 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Esters" by people in Profiles.
-
Foote PK, Krist DT, Statsyuk AV. High-Throughput Screening of HECT E3 Ubiquitin Ligases Using UbFluor. Curr Protoc Chem Biol. 2017 Sep 14; 9(3):174-195.
-
Jansone-Popova S, May JA. Synthesis of bridged polycyclic ring systems via carbene cascades terminating in C-H bond insertion. J Am Chem Soc. 2012 Oct 31; 134(43):17877-80.
-
Lundy BJ, Jansone-Popova S, May JA. Enantioselective conjugate addition of alkenylboronic acids to indole-appended enones. Org Lett. 2011 Sep 16; 13(18):4958-61.
-
Yost JM, Alfie RJ, Tarsis EM, Chong I, Coltart DM. Direct carbon-carbon bond formation via soft enolization: aldol addition of a-halogenated thioesters. Chem Commun (Camb). 2011 Jan 07; 47(1):571-2.
-
Sauer SJ, Garnsey MR, Coltart DM. Direct carbon-carbon bond formation via reductive soft enolization: a kinetically controlled syn-aldol addition of a-halo thioesters and enolizable aldehydes. J Am Chem Soc. 2010 Oct 13; 132(40):13997-9.
-
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.
-
Guo Y, Mietkiewska E, Francis T, Katavic V, Brost JM, Giblin M, Barton DL, Taylor DC. Increase in nervonic acid content in transformed yeast and transgenic plants by introduction of a Lunaria annua L. 3-ketoacyl-CoA synthase (KCS) gene. Plant Mol Biol. 2009 Mar; 69(5):565-75.
-
Tarsis E, Gromova A, Lim D, Zhou G, Coltart DM. Overcoming the limitations of the Morita-Baylis-Hillman reaction: a rapid and general synthesis of alpha-alkenyl-beta'-hydroxy thioesters. Org Lett. 2008 Nov 06; 10(21):4819-22.
-
Nipper ME, Majd S, Mayer M, Lee JC, Theodorakis EA, Haidekker MA. Characterization of changes in the viscosity of lipid membranes with the molecular rotor FCVJ. Biochim Biophys Acta. 2008 Apr; 1778(4):1148-53.
-
Kanan Y, Kasus-Jacobi A, Moiseyev G, Sawyer K, Ma JX, Al-Ubaidi MR. Retinoid processing in cone and Müller cell lines. Exp Eye Res. 2008 Feb; 86(2):344-54.
|
People  People who have written about this concept. _
Similar Concepts
People who have written about this concept.
_
Top Journals
Top journals in which articles about this concept have been published.
|