Assortment of Amides

Ready access to a diverse assortment of amides.

Ability to conduct the acyl substitution of carboxylic acids directly without product-isolation complications common to conventional dehydration methods.

 

Company Name

University of Notre Dame

Reference Number 1242

Market Sectors:

Chemicals

Operational Areas

Research
 

Commercial Solutions

Increase Efficiency
 
 

Description:

The technology allows for ready access to a diverse assortment of amides through the direct functionalization of carboxylic acids and azides by using a chlorophosphite as a dual activating agent, and results in simplified product isolation due to the aqueous solubility of the byproducts generated.

The bimodal reactivity of phosphite to unmask the latent electrophilicity of carboxylic acids and is directly applicable to the assembly of biologically active natural products and synthetic targets containing amides, lactams, and peptide linkages.

ADVANTAGES INCLUDE:

 - Ability to conduct the acyl substitution of carboxylic acids directly without product-isolation complications common to conventional dehydration methods.

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