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Functional group equivalents protected carboxylic acids

Functional groups can be protected carboxylic acids as oxazolines or silyl esters and alcohols as THP derivatives or potassium alkoxides. In fact, it may not be necessary to protect alcohols at all just use two equivalents of reagent The first will deprotonate the alcohol to give an alkoxyzirconium complex, and the second can then hydrozirconate the C=C or C C bond (equation 23). Several examples are shown in Tables 3 and 5. The presence of such functional groups does frequently have regio-chemical consequences, as will be shown in the following section. [Pg.683]


See other pages where Functional group equivalents protected carboxylic acids is mentioned: [Pg.147]    [Pg.478]    [Pg.150]    [Pg.442]    [Pg.598]    [Pg.75]    [Pg.354]    [Pg.10]    [Pg.50]    [Pg.51]    [Pg.533]    [Pg.190]    [Pg.172]    [Pg.219]    [Pg.355]    [Pg.617]    [Pg.158]   
See also in sourсe #XX -- [ Pg.157 ]




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Acidic function

Acidic functional groups

Acidic functionalities

Acidity functions

Acids carboxyl group

Carboxyl functional group

Carboxyl functionality

Carboxyl groups acidity

Carboxyl groups, protection

Carboxyl groups, protection Carboxylic acids

Carboxyl groups, protection functional group

Carboxyl protecting groups

Carboxylate functionality

Carboxylic acid functional group

Carboxylic acid groups

Carboxylic acids, protection

Carboxylic equivalent

Carboxylic functional groups

Carboxylic functionalities

Carboxylic functionalized

Carboxylic functions

Carboxylic-functionalization

Functional carboxylic acid

Functionalized carboxylate

Group equivalence

Protection function

Protective functions

Protective groups acids

Protective groups carboxylic acids

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