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Summary of Nucleophilic Substitution at Saturated Carbon

Dialkylation occurs if a stronger base (NaOH) and dimethyl sulfate is used. Entry 18 is a typical diazomethane methylation of a carboxylic acid. The toxicity of diazomethane [Pg.234]

Introduction of Functional Groups by Nucleophilic Substitution at Saturated Carbon [Pg.235]

Esterification by nucleophilic substitution with carboxylate salts [Pg.236]

SECTION 3.2. INTRODUCTION OF FUNCTIONAL GROUPS BY NUCLEOPHILIC SUBSTITUTION AT SATURATED CARBON [Pg.139]

Esterification by Nucleophilic Substitution with Carboxylate Salts [Pg.139]

CHAPTER 3 FUNCTIONAL GROUP INTERCONVERSION BY NUCLEOPHILIC SUBSTITUTION [Pg.140]


See other pages where Summary of Nucleophilic Substitution at Saturated Carbon is mentioned: [Pg.234]    [Pg.159]    [Pg.805]    [Pg.159]    [Pg.115]    [Pg.137]    [Pg.234]    [Pg.159]    [Pg.805]    [Pg.159]    [Pg.115]    [Pg.137]   


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At carbon

Carbon nucleophile

Carbon nucleophiles

Carbon nucleophiles, substitution

Carbon saturation

Nucleophilic Substitution at Carbon

Nucleophilic of carbonates

Nucleophilic substitution at saturated carbon

Nucleophilic substitution carbon

Nucleophilic substitution summary

Nucleophilicity at carbon

Saturated carbon

Saturated summary

Saturation of carbon

Substitution at

Substitution at carbon

Summary saturation

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