 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) |
G02.607.500.682
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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 |
|---|
| 1992 | 0 | 1 | 1 | | 1993 | 0 | 1 | 1 | | 1995 | 0 | 1 | 1 | | 1997 | 0 | 1 | 1 | | 1998 | 0 | 1 | 1 | | 2001 | 0 | 3 | 3 | | 2003 | 0 | 3 | 3 | | 2004 | 0 | 4 | 4 | | 2005 | 0 | 4 | 4 | | 2006 | 0 | 5 | 5 | | 2007 | 0 | 2 | 2 | | 2008 | 0 | 1 | 1 | | 2009 | 0 | 6 | 6 | | 2010 | 0 | 14 | 14 | | 2011 | 0 | 11 | 11 | | 2012 | 0 | 5 | 5 | | 2013 | 0 | 8 | 8 | | 2014 | 0 | 5 | 5 | | 2015 | 0 | 4 | 4 |
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Below are the most recent publications written about "Stereoisomerism" by people in Profiles.
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Rastelli EJ, Coltart DM. A Concise and Highly Enantioselective Total Synthesis of (+)-anti- and (-)-syn-Mefloquine Hydrochloride: Definitive Absolute Stereochemical Assignment of the Mefloquines. Angew Chem Int Ed Engl. 2015 Nov 16; 54(47):14070-4.
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Do H, Kang CW, Cho JH, Gilbertson SR. Enantioselective Synthesis of (-)-Dysiherbaine. Org Lett. 2015 Aug 21; 17(16):3972-4.
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Shih JL, Nguyen TS, May JA. Organocatalyzed Asymmetric Conjugate Addition of Heteroaryl and Aryl Trifluoroborates: a Synthetic Strategy for Discoipyrrole D. Angew Chem Int Ed Engl. 2015 Aug 17; 54(34):9931-5.
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Ku AF, Cuny GD. Synthetic studies of 7-oxygenated aporphine alkaloids: preparation of (-)-oliveroline, (-)-nornuciferidine, and derivatives. Org Lett. 2015 Mar 06; 17(5):1134-7.
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Han SJ, Vogt F, May JA, Krishnan S, Gatti M, Virgil SC, Stoltz BM. Evolution of a unified, stereodivergent approach to the synthesis of communesin F and perophoramidine. J Org Chem. 2015 Jan 02; 80(1):528-47.
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Grigorjeva L, Daugulis O. Cobalt-catalyzed, aminoquinoline-directed coupling of sp(2) C-H bonds with alkenes. Org Lett. 2014 Sep 05; 16(17):4684-7.
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Han SJ, Vogt F, Krishnan S, May JA, Gatti M, Virgil SC, Stoltz BM. A diastereodivergent synthetic strategy for the syntheses of communesin F and perophoramidine. Org Lett. 2014 Jun 20; 16(12):3316-9.
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Jones AC, May JA, Sarpong R, Stoltz BM. Toward a symphony of reactivity: cascades involving catalysis and sigmatropic rearrangements. Angew Chem Int Ed Engl. 2014 Mar 03; 53(10):2556-91.
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Zhao Y, Gilbertson SR. Synthesis of proline-based N-heterocyclic carbene ligands. Org Lett. 2014 Feb 21; 16(4):1033-5.
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Smuts JP, Na YC, Vallakati R, Pribylka A, May JA, Armstrong DW. Enantioseparation of flinderoles and borreverines by HPLC on Chirobiotic V and V2 stationary phases and by CE using cyclodextrin selectors. Anal Bioanal Chem. 2013 Nov; 405(28):9169-77.
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