Shi epoxidation

The Shi epoxidation is a

History

Oxoammonium salt

Catalyst generated from D-fructose

The reaction was first reported by Yian Shi (史一安, pinyin: Shǐ Yī-ān) of Colorado State University in 1996. Most catalyst candidates suffer from rapid decomposition/oxidation of the dioxirane intermediate and lack of electrophilicity of the reactive ketone. Aromatic ketones were proposed, and many subsequent variations of oxoammonium salts proved ineffective in promoting epoxidation because of the oxidative instability of the amide groups and high flexibility of the seven-membered rings. Enantioselectivity of these early catalysts were also lowered because of large distances between the asymmetric subunits and reaction centers, yielding less than 10 percent in enantiomeric excess.^[5]

The catalyst discovered by Yian Shi is derived from D-fructose and has a stereogenic center close to the reacting center (ketone)- the rigid six-membered ring structure of the catalyst and adjacent quaternary ring group minimizes epimerization of this stereocenter. Oxidation by the active dioxirane catalyst takes place from the si-face, due to steric hindrance of the opposing re-face. This catalyst functions efficiently as an asymmetric catalyst for unfunctionalized trans-olefins.^[6]

Dioxirane catalyst formation

Under normal pH conditions, an excess of 3 stoichiometric amounts of ketone catalyst are needed due to a high rate of decomposition. At basic pH conditions greater than 10 (pH 10.5) substoichiometric amounts (0.2–0.3) are needed for epoxidations, lowering the decomposition of reagents by disfavoring the Baeyer-Villiger side reaction. Higher temperatures result in further decomposition; thus a low temperature of zero degrees Celsius is used.

Decomposition of reagents is bimolecular (

The reaction is mediated by a D-fructose derived catalyst, which produces the (R,R) enantiomer of the resulting epoxide. Solubilities of olefin organic substrate and oxidant (oxone) differ, and thus a

The first step in the catalytic cycle reaction is the

A potential side reaction that may occur is the Baeyer-Villiger reaction of intermediate 2, where there is a rearrangement of the peroxy group that results in the formation of the relative ester. The extent of this side reaction declines with the rise of pH, and increases the nucleophilicity of the oxone, making basic conditions favorable for the overall epoxidation and reactivity of the catalytic species.

Epoxidation mechanisms

The oxygen from the dioxirane group generated on the organic catalyst is transferred to the alkene, in what is thought to be a concerted mechanism, although the presence of an oxygen anion intermediate through an S_n2 mechanism may transpire.

Preparation of D-fructose derivative

The catalyst is formed by reaction with acetone under basic conditions, with the hydroxyl groups of the fructose ring acting as nucleophiles, their nucleophilicity increased by the basic conditions created by potassium carbonate. The electron withdrawing substituents (alpha-ether groups) encourage the formation of the ketone from the oxidizing agent pyridinium chlorochromate by increasing the electrophilicity of the carbonyl carbon, via a stabilizing delocalization of the forming π C-C bonds into the σ* C-O bonds of the adjacent ethers.^[8]

Transition states and enantiomeric selectivity

There are two proposed transition states, whose geometries are speculated and not corroborated by experimental evidence, but are attributed to stereoelectronic effects. The spiro transition state is favored over the planar due to the non-bonding orbitals of the superior oxygen donating into the π* anti-bonding C-C orbitals of the reacting alkene, providing a stabilizing delocalization of electrons.

Donation of these electrons into the forming C-O σ bonds of the epoxide bonds also encourages the formation of the spiro-product (the geometry of the product is aligned as well). The planar configuration is disfavored due to lack of pi-backbonding and steric hindrance of the alkyl groups with large alkyl functional groups of the catalytic ring.^[9]

The previously mentioned configurations are favored over the transition states of the opposing enantiomers because of unfavorable steric interactions between the R-alkyl groups (see below) and the ether-alkyl functional groups of the catalyst ring.

The enantiomeric success of this epoxidation is relatively high compared to metal catalysts, and generally results in a high enantiomeric excess exceeding 80 percent.^[10]

Reaction yield and stereoselectivity

This procedure generates epoxides with high enantiomeric excesses from trans-disubstituted alkenes and trisubstituted alkenes. Cis-disubstituted alkenes^[11] and styrenes^[12] are asymmetrically epoxidized using a similar catalyst. Generation of (R,R) epoxides from corresponding alkenes increases in stereoselectivity with increased steric bulk of substituent R groups (especially in trans-olefins).

See also

• Sharpless epoxidation

References

1. doi:10.1021/ja962345g
   )
2. doi:10.1021/ja972272g
   )
3. "A New Type of Ketone Catalyst for Asymmetric Epoxidation". Wang Zhi-Xian, Shi Yian The Journal of Organic Chemistry 1997, 62(25), 8622–8623 (
   doi:10.1021/jo971701q
   )
4. doi:10.1021/ja003049d
   )
5. doi:10.1021/ol010066e
   )
6. doi:10.1055/s-1999-3123
   ; review)
7. doi:10.1055/s-2000-8715
   ; review)
8. ^ "Shi Epoxidation" at the Organic Chemistry Portal, <https://www.organic-chemistry.org/namedreactions/shi-epoxidation.shtm> (review)