Chiral auxiliary

A chiral auxiliary is a chemical compound or unit that is temporarily incorporated into an organic synthesis so that it can be carried out asymmetrically with the selective formation of one of two enantiomers^[1][2] . Chiral auxiliaries are optically active compounds and introduce chirality in otherwise racemic compounds. The temporary stereocenter then forces the asymmetric formation of a second stereocenter using steric hindrance or directing groups to determine chirality. After the creation of the second stereocenter the original auxiliary can be removed in a third step and recycled.

Chiral auxiliaries were introduced by E.J. Corey in 1978 with chiral 8-phenylmenthol and by B.M. Trost in 1980 with chiral mandelic acid. The menthol compound is difficult to prepare and an alternative is trans-2-phenyl-1-cyclohexanol introduced by J. K. Whitesell in 1985.

Contents 1 Oxazolidone auxiliaries 2 Pseudoephedrine auxiliaries 3 See also 4 References

Oxazolidone auxiliaries

A good example of chiral auxiliaries are the class of Evans auxiliaries comprising oxazolidinones substituted at the 4 and 5 positions. Through steric hindrance, the substituents direct the direction of substitution of various groups. The auxiliary is subsequently removed e.g. through hydrolysis.

Pseudoephedrine auxiliaries

Both (R,R)- and (S,S)-pseudoephedrine are used as a chiral auxiliary.^[3] Pseudoephedrine is reacted with a carboxylic acid, acid anhydride, or acyl chloride to give a pseudoephedrine amide.

The α-proton of the carbonyl compound is easily deprotonated by a non-nucleophilic base to give the enolate, which can further react. The configuration of the addition compound, such as with an alkyl halide, is directed by the methyl group. Thus, any addition product will be anti to the methyl and syn with the hydroxyl group. The pseudoephedrine chiral auxiliary is subsequently removed by cleaving the amide bond with an appropriate nucleophile.

In the original work by Myers (1994) one of the substrates was propionic acid:

The amide not only can be hydrolysed but also reduced to the aldehyde (Lithium aluminium hydride alkoxide) or to the alcohol (borane complex with Pyrrolidine).

In one study the chiral auxiliary is (-)-ephedrine:^[4]

See also

• Example of use of trans-2-Phenyl-1-cyclohexanol as chiral auxiliary: Ojima lactam
• Valine as a Chiral auxiliary in the Schöllkopf method
• Tert-butanesulfinamide as reagent for asymmetric synthesis of amines

Concepts in asymmetric synthesis Chirality types Chirality · Stereocenter · Planar chirality · Chiral ligand · Axial chirality · Supramolecular chirality · Inherent chirality Chiral molecules Stereoisomer · Enantiomer · Diastereomer · Meso compound · Enantiomeric excess · Diastereomeric excess · Analysis Optical rotation · Chiral derivatizing agents · NMR spectroscopy of stereoisomers · Ultraviolet-visible spectroscopy of stereoisomers Chiral resolution Recrystallization · Kinetic resolution · Chiral column chromatography · Diastereomeric recrystallization Reactions Asymmetric induction · Chiral pool synthesis · Chiral auxiliaries · Asymmetric catalysis · Organocatalysis · Biocatalysis

References

1. ^ Compendium of chiral auxiliary applications (ed.: Roos, G.), Academic Press, New York, 2002.
2. ^ Chiral auxiliaries - principles and recent applications; Gnas, Y.; Glorius, F. Synthesis 2006, 1899 doi:10.1055/s-2006-942399.
3. ^ Myers, A. G., et al., Pseudoephedrine as a Practical Chiral Auxiliary for the Synthesis of Highly Enantiomerically Enriched Carboxylic Acids, Alcohols, Aldehydes, and Ketones, J. Am. Chem. Soc., 1997, 119, 6496-6511.doi:10.1021/ja970402f
4. ^ Chiral Polycyclic Ketones via Desymmetrization of Dihaloolefins Giuseppe Borsato, Anthony Linden, Ottorino De Lucchi, Vittorio Lucchini, David Wolstenholme, and Alfonso Zambon J. Org. Chem.; 2007; 72(11) pp 4272 - 4275; (Note) doi:10.1021/jo070222g