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  2. Meso compound - Wikipedia

    en.wikipedia.org/wiki/Meso_compound

    A meso compound or meso isomer is an optically inactive isomer in a set of stereoisomers, at least two of which are optically active. [1] [2] This means that despite containing two or more stereocenters, the molecule is not chiral. A meso compound is superposable on its mirror image (not to be confused with superimposable, as any two objects ...

  3. Stereoisomerism - Wikipedia

    en.wikipedia.org/wiki/Stereoisomerism

    These include meso compounds, cis–trans isomers, E-Z isomers, and non-enantiomeric optical isomers. Diastereomers seldom have the same physical properties. In the example shown below, the meso form of tartaric acid forms a diastereomeric pair with both levo- and dextro-tartaric acids, which form an enantiomeric pair.

  4. Inositol - Wikipedia

    en.wikipedia.org/wiki/Inositol

    In biochemistry, medicine, and related sciences, inositol generally refers to myo-inositol (formerly meso-inositol), the most important stereoisomer of the chemical compound cyclohexane-1,2,3,4,5,6-hexol. Its formula is C 6 H 12 O 6; the molecule has a ring of six carbon atoms, each with an hydrogen atom and a hydroxyl group (–OH).

  5. 2,3-Epoxybutane - Wikipedia

    en.wikipedia.org/wiki/2,3-Epoxybutane

    The compound exists as three stereoisomers, a pair of enantiomers and the meso isomer. All are colorless liquids. Preparation and reactions 2,3 ...

  6. Enantiomer - Wikipedia

    en.wikipedia.org/wiki/Enantiomer

    There are three common naming conventions for specifying one of the two enantiomers (the absolute configuration) of a given chiral molecule: the R/S system is based on the geometry of the molecule; the (+)- and (−)- system (also written using the obsolete equivalents d- and l-) is based on its optical rotation properties; and the D/L system is based on the molecule's relationship to ...

  7. 2,3-Butanediol - Wikipedia

    en.wikipedia.org/wiki/2,3-Butanediol

    Of the three stereoisomers, two are enantiomers (levo- and dextro-2,3-butanediol) and one is a meso compound. [ 1 ] [ 2 ] The enantiomeric pair have (2 R , 3 R ) and (2 S , 3 S ) configurations at carbons 2 and 3, while the meso compound has configuration (2 R , 3 S ) or, equivalently, (2 S , 3 R ).

  8. Meso isomer - Wikipedia

    en.wikipedia.org/?title=Meso_isomer&redirect=no

    This page was last edited on 23 November 2016, at 13:55 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  9. meso-Zeaxanthin - Wikipedia

    en.wikipedia.org/wiki/Meso-zeaxanthin

    The meso-form is the second most abundant in nature, after 3R,3′R-zeaxanthin, which is produced by plants and algae. [1] Meso-zeaxanthin has been identified in specific tissues of marine organisms [2] and in the macula lutea, also known as the "yellow spot" of the human retina. [3] [4]