This type of reaction is also called a 1,2 nucleophilic addition.

The process is an example of a nucleophilic addition to a carbonyl.

Once this conformation is established, one can consider the nucleophilic addition.

Nucleophilic addition is also a good reaction, though a bit more difficult than with ketones.

This species reacts with the carbonyl group in a nucleophilic addition.

It has been used in nucleophilic addition to ketones.

Nucleophilic addition to pi ligands can be used in synthesis.

Nucleophilic addition to an epoxide can be base or acid catalyzed.

There are many variations of nucleophilic addition reactions.

Subsequent to nucleophilic addition, the modified arene can be recovered from the metal.

They undergo nucleophilic addition and substitution reactions with various electrophiles.

Nucleophilic additions to arynes have been widely used in natural product total synthesis.

A nucleophile in a nucleophilic addition can approach the carbonyl group from two opposite sides or faces.

Tetrahedral intermediates result from nucleophilic addition to a carbonyl group.

The protonated carbonyl group 2 is activated for nucleophilic addition of the alcohol.

The conformational change involves a 1,2 nucleophilic addition.

The reaction is a sequence of nucleophilic additions.

It is easy to do nucleophilic additions to it, which makes the molecule bigger.

Chlorobutanol is formed by the simple nucleophilic addition of chloroform and acetone.

A second nucleophilic addition takes place at this intermediate with the carboxylic acid anion to 8.

The reaction type is nucleophilic addition.

Oxidative addition is also needed in order for nucleophilic addition of an alkyl group to occur.

Additions across pi bonds appear to proceed by typical nucleophilic addition pathways in most cases.

The nucleophilic addition of urea gives the intermediate 4, which quickly dehydrates to give the desired product 5.

This scheme begins with rate determining nucleophilic addition by the urea to the aldehyde.