Tsuji–Trost reaction

Tsuji–Trost Reaction is a significant chemical reaction in the field of organic chemistry, named after Jiro Tsuji and David A. Trost, who independently developed this reaction. It is a palladium-catalyzed substitution reaction that allows for the allylation of nucleophiles. This reaction is particularly useful for the formation of carbon-carbon (C-C) bonds, making it a valuable tool in the synthesis of complex organic molecules, including natural products and pharmaceuticals.

Overview

The Tsuji–Trost reaction involves the nucleophilic attack on an allylic substrate that is coordinated to a palladium catalyst. The general mechanism includes the oxidative addition of the palladium catalyst to an allylic leaving group, followed by the formation of a π-allyl palladium complex. A nucleophile then attacks this complex, leading to the reductive elimination and formation of a new C-C bond. The versatility of this reaction stems from its ability to use a wide range of nucleophiles, including carbon, nitrogen, oxygen, and sulfur-based nucleophiles.

Mechanism

1. Oxidative addition: The palladium(0) catalyst reacts with an allylic electrophile, forming a π-allyl palladium complex.
2. Nucleophilic attack: A nucleophile attacks the π-allyl palladium intermediate, leading to the formation of a new C-C bond.
3. Reductive elimination: The palladium catalyst is regenerated, and the product is released.

Applications

The Tsuji–Trost reaction has found extensive applications in organic synthesis. It is particularly useful in the synthesis of complex molecules such as natural products, pharmaceuticals, and polymers. Its ability to form C-C bonds in a stereoselective manner makes it a valuable tool in the construction of chiral molecules.

Variants

Several variants of the Tsuji–Trost reaction have been developed to increase its scope and efficiency. These include:

• Asymmetric Tsuji–Trost reactions, which use chiral ligands to induce stereoselectivity in the product.
• Intramolecular Tsuji–Trost reactions, where the nucleophile and the allylic substrate are part of the same molecule, leading to the formation of cyclic products.

Limitations

Despite its versatility, the Tsuji–Trost reaction has some limitations. The need for a palladium catalyst can make the reaction expensive. Additionally, the reaction conditions need to be carefully controlled to avoid side reactions and ensure high selectivity.

See Also

• Palladium-catalyzed coupling reactions
• Carbon-carbon bond formation
• Organic synthesis
• Stereoselectivity

References

This article is a stub related to chemistry. You can help WikiMD by expanding it!

• 

  Tsuji–Trost reaction

• 

  Tsuji 1965

• 

  Trost 1973

• 

  Tsuji–Trost catalytic cycle

• 

  Hard vs Soft Nucleophile

• 

  Expanded Nucleophile Scope

• 

  AAA allene

• 

  Trost AAA galanthamine Intermediate

• 

  Tsuji–Trost reaction

• 

  Tsuji–Trost reaction