2,3-sigmatropic rearrangement

2,3-Sigmatropic rearrangements are a type of sigmatropic rearrangements and can be classified into two types. Rearrangements of allylic sulfoxides, amine oxides, selenoxides are neutral. Rearrangements of carbanions of allyl ethers are anionic. The general scheme for this kind of rearrangement is:

Additional recommended knowledge

Weighing the right way

Don't let static charges disrupt your weighing accuracy

How to ensure accurate weighing results every day?

Atom Y may be sulfur, selenium, or nitrogen. If Y is nitrogen, the reaction is referred to as a 2,3-Stevens rearrangement; if Y is oxygen, then it is called a 2,3-Wittig rearrangement (not to be confused with the well-known Wittig reaction, which involves a phosphonium ylide).

A [2,3]-rearrangement may result in carbon-carbon bond formation. It can also be used as a ring-expansion reaction.

Stereoselectivity

2,3-Sigmatropic rearrangements can offer high stereoselectivity. At the newly formed double bond there is a strong preference for formation of the E-alkene or trans isomer product. The stereochemistry of the newly formed C-C bond is harder to predict. It can be inferred from the five-membered ring transition state. Generally, the E-alkene will favor the formation of anti product, while Z-alkene will favor formation of syn product.

Diastereoselectivity can be high for Z-alkene with alkynyl, alkenl, or aryl anion-stabilizing group. Diastereoselectivity is usually lower with E-alkenes. Hydrocarbon groups will prefer exo orientation in the envelope-like transition state. Anion-stabilizing group will prefer the endo orientation in transition state.