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STEGLICH ESTERIFICATION

Steglich esterification

Chemical reaction

The Steglich esterification is a variation of an esterification with dicyclohexylcarbodiimide as a coupling reagent and 4-dimethylaminopyridine as a catalyst

Steglich esterification

Steglich_esterification

Fischer–Speier esterification

Type of chemical reaction

substrates (for example, biomaterials) other, milder procedures such as Steglich esterification are used. The reaction is often carried out without a solvent (particularly

Fischer–Speier esterification

Fischer–Speier_esterification

Ester

Compound derived from an acid

mixtures of alcohols and carboxylic acids. One example is the Steglich esterification, which is a method of forming esters under mild conditions. The

Ester

Wolfgang Steglich

German chemist (born 1933)

Wolfgang Steglich retired in 2001. The use of 4-dimethylaminopyridine for esterifications with anhydrides, which is sometimes called the Steglich esterification

Wolfgang Steglich

Wolfgang_Steglich

Shiina esterification

Shiina macrolactonization Fischer–Speier esterification Steglich esterification Yamaguchi esterification Mitsunobu reaction Shiina, I.; Miyoshi, S.;

Shiina esterification

Shiina_esterification

N,N'-Dicyclohexylcarbodiimide

Chemical compound

products. DCC can also be used to invert secondary alcohols. In the Steglich esterification, alcohols, including even some tertiary alcohols, can be esterified

N,N'-Dicyclohexylcarbodiimide

List of organic reactions

synthesis Stahl oxidation Staudinger reaction Staudinger synthesis Steglich esterification Stephen aldehyde synthesis Stephens-Castro coupling Stetter reaction

List of organic reactions

List_of_organic_reactions

4-Dimethylaminopyridine

Chemical compound

of reactions such as esterifications with anhydrides, the Baylis-Hillman reaction, hydrosilylations, tritylation, the Steglich rearrangement, Staudinger

4-Dimethylaminopyridine

Propyl gallate

Chemical compound

have been the most prominent methods of production, and include Steglich esterification with N,N'-diisopropylcarbodiimide and 4-dimethylaminopyridine,

Propyl gallate

Propyl_gallate

Shiina macrolactonization

(PPY) are employed. Shiina esterification Fischer-Speier esterification Steglich esterification Yamaguchi esterification Mitsunobu reaction Shiina, I

Shiina macrolactonization

Shiina_macrolactonization

Pyridines

Class of chemical substances

are also known. A related and important named reaction is the Steglich esterification, in which an alcohol and a carboxylic acid are esterified using

Pyridines

2-Methyl-6-nitrobenzoic anhydride

Chemical compound

esterification Mitsunobu reaction Shiina esterification Steglich esterification Yamaguchi esterification "Named Reagents". OChemOnline. Archived from the original

2-Methyl-6-nitrobenzoic anhydride

2-Methyl-6-nitrobenzoic_anhydride

Vulpinic acid

Chemical compound

bright yellow in color. Vulpinic acid is derived biosynthetically by esterification from pulvinic acid; pulvinate itself derives from the aromatic amino

Vulpinic acid

Vulpinic_acid

Organocatalysis

Method in organic chemistry

200906900. PMID 20175175. Neises, Bernhard; Steglich, Wolfgang (July 1978). "Simple Method for the Esterification of Carboxylic Acids". Angewandte Chemie

Organocatalysis