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In chemistry, an enantiomer (/, , / ə-NAN-tee-ə-mər; from Greek ἐνάντιος (enántios), meaning "opposite", and μέρος (méros), meaning "part"), also known as an optical isomer, is one of two stereoisomers that are mirror images of each other that are non-superposable (not identical), much as one's left and right hands are the same except for being reversed along one axis (the hands cannot be made to appear identical simply by reorientation). Organic compounds that contain a chiral carbon atom usually have two non-superposable structures. These two structures are mirror images of each other and are, thus, commonly called enantiomorphs (enantio = opposite ; morph = form), hence this structural property is now commonly referred to as enantiomerism.
When present in a symmetric environment, enantiomers have identical chemical and physical properties except for their ability to rotate plane-polarized light (+/−) by equal amounts but in opposite directions (although the polarized light can be considered an asymmetric medium). They are sometimes called optical isomers for this reason. A mixture of equal parts of an optically active isomer and its enantiomer is termed racemic and has zero net rotation of plane-polarized light because the positive rotation of each (+) form is exactly counteracted by the negative rotation of a (−) one.
When a steriochemical has both optical isomerism and geometric isomerism incorporated in its' structure it gives rise to enantiomerism or steriospecificity for a better word choice. If a steriochemical has three isomeric identities (n=3) i.e. a dextro chiral center and an axial substitution on a trans ring then the steriochemical has both one optical isomer center and two geometric isomers or identifications this makes three variables or n=3,(geometric isomerism gives rise to axial and equatorial isomers as well as cis and trans isomers if it is an alkane ring or the carbon atoms are single bonds). So theoretically you can have for example cis axial and cis equatorial and further dextro cis axial and dextro cis equatorial and the chiral center has to be on a different carbon center than the carbon center that has the substituted axial or equatorial conformer hypothetically. Further the n=2 gives rise to four stereospecific conformers or enantiomers which are four different molecules in the steriochemical sense and can be drawn three dimentially four different ways and they are not superimposable because you get cis dextro, trans dextro, cis levo or trans levo. For example say you have cis dextro this gives rise to n=2 then one can draw four different enantiomers. If n=3 then this gives rise to 8 enantiomers, n=4 gives rise to 16, n=5 gives rise to 32 and if n=6 this gives rise to 64 drawings or icons and so on as the value of "n" increases and each conclusion is non-superimposable. These rules change if one has glucose for example where it has both an optical isomer and geometric isomer on the same isolated carbon center. So one carbon center has for example an axial hydroxyl group and dextro chirality. So if we take glucose the base isomer variable number is 6 (n=6) and as previously stated, n=6 gives rise to 64 enantiomers or stereospecific icons. The glucose molecule has 5 chiral centers and 1 geometric variable (cis or trans); so n=6. Additionally, the reason being in regards to the glucose stereoisomer the five chiral centers can give rise to axial or equatorial hydroxyl conformers but the two variables i.e. dextro axial rules its' self out because the two variables are on the same carbon atom. This is a unique situation. 
Enantiomer members often have different chemical reactions with other enantiomer substances. Since many biological molecules are enantiomers, there is sometimes a marked difference in the effects of two enantiomers on biological organisms. In drugs, for example, often only one of a drug's enantiomers is responsible for the desired physiologic effects, while the other enantiomer is less active, inactive, or sometimes even productive of adverse effects. Owing to this discovery, drugs composed of only one enantiomer ("enantiopure") can be developed to enhance the pharmacological efficacy and sometimes eliminate some side effects. An example is eszopiclone (Lunesta), which is enantiopure and therefore administered in doses that are exactly 1/2 of the older, racemic mixture called zopiclone. In the case of eszopiclone, the S enantiomer is responsible for all the desired effects, while the other enantiomer seems to be inactive. A dose of 2 mg of zopiclone must be administered to produce the same therapeutic effect as 1 mg of eszopiclone, and that appears to be the only difference between the two drugs.
In chemical synthesis of enantiomeric substances, non-enantiomeric precursors inevitably produce racemic mixtures. In the absence of an effective enantiomeric environment (precursor, chiral catalyst, or kinetic resolution), separation of a racemic mixture into its enantiomeric components is impossible.
The R/S system is an important nomenclature system for denoting enantiomers. Another system is based on optical activity: (+)- and (−)- or d- and l-. The Latin for left and right is laevus and dexter, respectively. Left and right have always had moral connotations, and the Latin words for these are sinister and rectus (straight, proper). The English word right is a cognate of rectus. This is the origin of the D,L and S,R notations.
Criterion of enantiomerism
Most compounds that contain one or more asymmetric carbon atoms show enantiomerism, but this is not always true. There are a few known compounds that do have asymmetric carbon atoms, but, being non-dissymmetric with respect to the whole molecule, do not show enantiomerism. Thus, meso tartaric acid has two asymmetric carbon atoms, but samples still exhibit optical inactivity because each of the two halves of the molecule is equal and opposite to the other and thus is superimposable on its geometric mirror image.
An example of such an enantiomer is the sedative thalidomide, which was sold in a number of countries across the world from 1957 until 1961. It was withdrawn from the market when it was found to cause of birth defects. One enantiomer caused the desirable sedative effects, while the other, unavoidably present in equal quantities, caused the birth defects.
Another example is the antidepressant drugs escitalopram and citalopram. Citalopram is a racemate [1:1 mixture of (S)-citalopram and (R)-citalopram]; escitalopram [(S)-citalopram] is a pure enantiomer. The dosages for escitalopram are typically 1/2 of those for citalopram.
There are two main strategies for the preparation of enantiopure compounds. The first is known as chiral resolution. This method involves preparing the compound in racemic form, and separating it into its isomers. In his pioneering work, Louis Pasteur was able to isolate the isomers of tartaric acid because they crystallize from solution as crystals each with a different symmetry. A less common method is by enantiomer self-disproportionation.
The second strategy is asymmetric synthesis: the use of various techniques to prepare the desired compound in high enantiomeric excess. Techniques encompassed include the use of chiral starting materials (chiral pool synthesis), the use of chiral auxiliaries and chiral catalysts, and the application of asymmetric induction. The use of enzymes (biocatalysis) may also produce the desired compound.
Enantioconvergent synthesis is the synthesis of one enantiomer from a racemic precursor molecule utilizing both enantiomers. Thus, the two enantiomers of the reactant produce a single enantiomer of product.
Advances in industrial chemical processes have made it economical for pharmaceutical manufacturers to take drugs that were originally marketed as a racemic mixture and market the individual enantiomers. In some cases, the enantiomers have genuinely different effects. In other cases, there may be no clinical benefit to the patient. In some jurisdictions, single-enantiomer drugs are separately patentable from the racemic mixture. It is possible that only one of the enantiomers is active. Or, it may be that both are active, in which case separating the mixture has no objective benefits, but extends the drug's patentability.
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