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  2. Absolute configuration - Wikipedia

    en.wikipedia.org/wiki/Absolute_configuration

    Examples of absolute configuration of some carbohydrates and amino acids according to Fischer projection (D/L system) and Cahn–Ingold–Prelog priority rules (R/S system) The R/S system is an important nomenclature system for denoting enantiomers. This approach labels each chiral center R or S according to a system by which its substituents ...

  3. 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 ...

  4. Indacrinone - Wikipedia

    en.wikipedia.org/wiki/Indacrinone

    As indicated earlier, the (R)- enantiomer is the pharmacologically active diuretic. Like most other diuretics, the (R)-isomer possesses an undesirable side-effect of retaining uric acid. But the (S)-enantiomer, the distomer , has the property of assisting uric acid secretion (uricosuric effect), and, therefore, antagonizing the undesirable side ...

  5. Nuclear magnetic resonance spectroscopy of stereoisomers

    en.wikipedia.org/wiki/Nuclear_magnetic_resonance...

    Mosher's acid contains a -CF 3 group, so if the adduct has no other fluorine atoms, the 19 F NMR of a racemic mixture shows just two peaks, one for each stereoisomer. As with NMR spectroscopy in general, good resolution requires a high signal-to-noise ratio , clear separation between peaks for each stereoisomer, and narrow line width for each peak.

  6. Racemic mixture - Wikipedia

    en.wikipedia.org/wiki/Racemic_mixture

    In chemistry, a racemic mixture or racemate (/ r eɪ ˈ s iː m eɪ t, r ə-, ˈ r æ s ɪ m eɪ t / [1]) is one that has equal amounts of left- and right-handed enantiomers of a chiral molecule or salt. Racemic mixtures are rare in nature, but many compounds are produced industrially as racemates.

  7. Glyceraldehyde - Wikipedia

    en.wikipedia.org/wiki/Glyceraldehyde

    Glyceraldehyde has one chiral center and therefore exists as two different enantiomers with opposite optical rotation: In the D/L nomenclature, either D from Latin Dexter meaning "right", or L from Latin Laevo meaning "left" In the R/S nomenclature, either R from Latin Rectus meaning "right", or S from Latin Sinister meaning "left"

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    The search engine that helps you find exactly what you're looking for. Find the most relevant information, video, images, and answers from all across the Web.

  9. Solketal - Wikipedia

    en.wikipedia.org/wiki/Solketal

    Solketal is a protected form of glycerol with an isopropylidene acetal group joining two neighboring hydroxyl groups. Solketal contains a chiral center on the center carbon of the glycerol backbone, and so can be purchased as either the racemate or as one of the two enantiomers.

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