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Hydroxy-amides, from addition amino-alcohols

There are several types of chiral derivatizing reagents commonly used depending on the functional group involved. For amines, the formation of an amide from reaction with an acyl halide [147,148], chloroformate reaction to form a carbamate [149], and reaction with isocyanate to form the corresponding urea are common reactions [150]. Carboxyl groups can be effectively esterified with chiral alcohols [151-153]. Isocynates have been used as reagents for enantiomer separation of amino acids, iV-methylamino acids, and 3-hydroxy acids [154]. In addition to the above-mentioned reactions, many others have been used in the formation of derivatives for use on a variety of packed and capillary columns. For a more comprehensive list, refer to References 155-159. [Pg.58]


See other pages where Hydroxy-amides, from addition amino-alcohols is mentioned: [Pg.324]    [Pg.179]    [Pg.86]    [Pg.138]    [Pg.377]    [Pg.380]    [Pg.382]    [Pg.288]   


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2-Amino- -amid

Addition alcohols

Alcohol additive

Alcohols amidation

Alcohols amino alcohol

Alcohols from amides

Alcohols, from addition

Amidations alcohols

Amides addition

Amino alcohols

Amino hydroxy

From amides

Hydroxy amides

Hydroxy-, alcoholate

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