Petasis reaction

A chemical reaction used in organic synthesis

Petasis reaction

The Petasis reaction is a multi-component organic reaction that involves the coupling of an amine, a vinyl boronic acid, and a carbonyl compound (typically an aldehyde or ketone) to form a variety of valuable products, including amino acids, amines, and diols. This reaction is named after Nicos A. Petasis, who first reported it in the mid-1990s. The Petasis reaction is notable for its mild reaction conditions, broad substrate scope, and high tolerance to functional groups, making it a powerful tool in the synthesis of complex organic molecules.

Petasis Reaction Scheme

Alphaaminoacidsynthesis

Organoboronic_acid_synthesis

E-Allylamines

Petasis-naftifine

Mechanism

The Petasis reaction proceeds through a Lewis acid-catalyzed process where the vinyl boronic acid reacts with the carbonyl compound to form an intermediate that subsequently reacts with the amine. This sequence leads to the formation of a new carbon-nitrogen bond and the incorporation of the vinyl group into the product. The reaction is highly stereoselective and can be used to synthesize both chiral and achiral products.

Applications

The Petasis reaction has found widespread application in the synthesis of natural products, pharmaceuticals, and other biologically active molecules. Its ability to efficiently construct complex molecules from simple precursors has made it a valuable tool in medicinal chemistry, organic synthesis, and material science. The reaction's versatility allows for the synthesis of a wide range of compounds, including peptidomimetics, heterocycles, and polyols, among others.

Advantages

One of the key advantages of the Petasis reaction is its operational simplicity and the mildness of the reaction conditions, which often occur at room temperature and in the presence of water or other benign solvents. Additionally, the reaction's high chemoselectivity and functional group tolerance enable the synthesis of multifunctional compounds without the need for protecting groups. The use of vinyl boronic acids as reagents also contributes to the reaction's sustainability, as boronic acids are relatively benign and easy to handle.

Limitations

While the Petasis reaction is broadly applicable, it does have some limitations. The availability of vinyl boronic acids can sometimes be a limiting factor, although recent advances in the synthesis and commercial availability of these reagents have mitigated this issue. Additionally, the reaction's stereoselectivity can be influenced by the choice of substrates and reaction conditions, requiring careful optimization for the synthesis of enantiomerically pure compounds.

Gallery

• 
  Aryl glycine rxn scheme
• 
  Clopidogrel synthesis
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  Diastereoselectivealphaaminoacids
• 
  N-sub indole Petasis-acid formation
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  Petasis with tri-substituted aromatic amine
• 
  Enalaprilat scheme

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