Acylation and Alkylation

Michael Röper

Michael Röper

BASF Aktiengesellschaft, Ludwigshafen, Germany

Search for more papers by this author
Eugen Gehrer

Eugen Gehrer

BASF Aktiengesellschaft, Ludwigshafen, Germany

Search for more papers by this author
Thomas Narbeshuber

Thomas Narbeshuber

BASF Aktiengesellschaft, Ludwigshafen, Germany

Search for more papers by this author
Wolfgang Siegel

Wolfgang Siegel

BASF Aktiengesellschaft, Ludwigshafen, Germany

Search for more papers by this author
First published: 15 June 2000
Citations: 5

Abstract

The article contains sections titled:

1.

Introduction

1.1.

Catalysts

1.1.1.

Acidic Catalysts

1.1.2.

Basic Catalysts

1.1.3.

Organometallic Catalysts

1.2.

Alkylating and Acylating Agents

1.3.

Mechanism

1.3.1.

Alkylation

1.3.2.

Acylation

2.

Alkylation and Acylation of Aromatic Compounds

2.1.

Alkylation

2.1.1.

Alkylation of Benzene

2.1.2.

Cycloalkylation

2.1.3.

Alkylation of Substituted Benzenes

2.1.4.

Alkylation of Phenols

2.1.5.

Alkylation of Aromatic Amines

2.1.6.

Alkylation of Heteroaromatic Compounds and Related Substrates

2.1.7.

Miscellaneous Alkylation Reactions

2.2.

Acylation

2.2.1.

Acylation of Benzene and Benzene Derivatives

2.2.2.

Acylation of Polynuclear Aromatic Compounds

2.2.3.

Acylation of Heteroaromatic Compounds

2.2.4.

Acylation of Nonbenzenoid Aromatic Compounds

2.2.5.

Miscellaneous Acylation Reactions

3.

Acylation and Alkylation of Aliphatic Hydrocarbons

4.

N-Alkylation and N-Acylation

4.1.

N-Alkylation

4.1.1.

N-Alkylation by Alcohols or Ethers

4.1.2.

N-Alkylation by Alkyl Halides

4.1.3.

N-Alkylation by Olefins

4.1.4.

N-Alkylation by Carbonyl Compounds (Reductive Alkylation)

4.2.

N-Acylation

5.

O-Alkylation and O-Acylation

5.1.

Synthesis of Esters

5.2.

Synthesis of Anhydrides

5.3.

Synthesis of Ethers

6.

CH-Alkylation and CH-Acylation of Nonaromatic Compounds

7.

Synthesis of Metal Alkyls

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.