 Stereoisomerism
"Stereoisomerism" 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 phenomenon whereby compounds whose molecules have the same number and kind of atoms and the same atomic arrangement, but differ in their spatial relationships. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 5th ed)
| Descriptor ID |
D013237
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| MeSH Number(s) |
G02.607.445.682
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Stereoisomerism".
Below are MeSH descriptors whose meaning is more specific than "Stereoisomerism".
This graph shows the total number of publications written about "Stereoisomerism" by people in this website by year, and whether "Stereoisomerism" 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 |
|---|
| 1995 | 0 | 1 | 1 | | 1996 | 0 | 3 | 3 | | 1999 | 0 | 2 | 2 | | 2001 | 0 | 1 | 1 | | 2002 | 0 | 1 | 1 | | 2003 | 0 | 4 | 4 | | 2004 | 0 | 3 | 3 | | 2005 | 0 | 6 | 6 | | 2006 | 0 | 5 | 5 | | 2007 | 0 | 4 | 4 | | 2008 | 0 | 3 | 3 | | 2009 | 0 | 2 | 2 | | 2010 | 0 | 3 | 3 | | 2011 | 0 | 11 | 11 | | 2012 | 0 | 1 | 1 | | 2013 | 0 | 5 | 5 | | 2015 | 0 | 1 | 1 | | 2016 | 0 | 2 | 2 | | 2017 | 0 | 1 | 1 | | 2018 | 0 | 5 | 5 | | 2019 | 0 | 6 | 6 | | 2020 | 0 | 1 | 1 | | 2021 | 0 | 2 | 2 | | 2023 | 0 | 1 | 1 |
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Below are the most recent publications written about "Stereoisomerism" by people in Profiles.
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Kuatsjah E, Zahn M, Chen X, Kato R, Hinchen DJ, Konev MO, Katahira R, Orr C, Wagner A, Zou Y, Haugen SJ, Ramirez KJ, Michener JK, Pickford AR, Kamimura N, Masai E, Houk KN, McGeehan JE, Beckham GT. Biochemical and structural characterization of a sphingomonad diarylpropane lyase for cofactorless deformylation. Proc Natl Acad Sci U S A. 2023 01 24; 120(4):e2212246120.
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Tcheng M, Cunha VLS, Ahmed N, Liu X, Smith RW, Rea KA, Akhtar TA, D'Alessandro A, Minden MD, Vockley J, O'Doherty GA, Lowary TL, Spagnuolo PA. Structure-activity relationship of avocadyne. Food Funct. 2021 Jul 21; 12(14):6323-6333.
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Miller EM, Walczak MA. Light-Mediated Cross-Coupling of Anomeric Trifluoroborates. Org Lett. 2021 06 04; 23(11):4289-4293.
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Meissner K, Henthorn TK. How relevant is stereoselectivity to the side-effects of ketamine? Br J Anaesth. 2021 07; 127(1):1-2.
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Zhu F, Walczak MA. Stereochemistry of Transition Metal Complexes Controlled by the Metallo-Anomeric Effect. J Am Chem Soc. 2020 09 02; 142(35):15127-15136.
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Prates ET, Crowley MF, Skaf MS, Beckham GT. Catalytic Mechanism of Aryl-Ether Bond Cleavage in Lignin by LigF and LigG. J Phys Chem B. 2019 12 05; 123(48):10142-10151.
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Li S, Liu J, Ramesar NS, Heinz H, Xu L, Xu C, Kotov NA. Single- and multi-component chiral supraparticles as modular enantioselective catalysts. Nat Commun. 2019 10 23; 10(1):4826.
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Zhang X, Peng Y, Grace PM, Metcalf MD, Kwilasz AJ, Wang Y, Zhang T, Wu S, Selfridge BR, Portoghese PS, Rice KC, Watkins LR, Hutchinson MR, Wang X. Stereochemistry and innate immune recognition: (+)-norbinaltorphimine targets myeloid differentiation protein 2 and inhibits toll-like receptor 4 signaling. FASEB J. 2019 08; 33(8):9577-9587.
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Koneru PC, Francis AC, Deng N, Rebensburg SV, Hoyte AC, Lindenberger J, Adu-Ampratwum D, Larue RC, Wempe MF, Engelman AN, Lyumkis D, Fuchs JR, Levy RM, Melikyan GB, Kvaratskhelia M. HIV-1 integrase tetramers are the antiviral target of pyridine-based allosteric integrase inhibitors. Elife. 2019 05 23; 8.
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Brandt K, D?tterl S, Fuchs R, Navarro DMDAF, Machado ICS, Dobler D, Reiser O, Ayasse M, Milet-Pinheiro P. Subtle Chemical Variations with Strong Ecological Significance: Stereoselective Responses of Male Orchid Bees to Stereoisomers of Carvone Epoxide. J Chem Ecol. 2019 Jun; 45(5-6):464-473.
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