Diels-Alder reaction

Since that time, use of the Diels-Alder reaction has become widespread.

Also, acceleration of Diels-Alder reactions by water has been observed.

Most notable is the Diels-Alder reaction with 1,3-dienes to give 1,4-cyclohexadienes.

It can be produced using the Diels-Alder reaction, and has at least 147 constituents.

They do that with cycloaddition reactions, similar to the Diels-Alder reaction.

Himbacine has been synthesized using a Diels-Alder reaction as a key step.

This organic synthesis is known as the Diels-Alder reaction.

Diels-Alder reactions are thermal reaction; the reaction is initiated by heat.

The Diels-Alder reaction is used to produce it.

The insecticide aldrin, created through a Diels-Alder reaction, is also named for him.

Using a retro Diels-Alder reaction, structure 5 was formed in near quantitative yield.

In asymmetric Diels-Alder reactions only one of two possible enantiomers is formed.

They are commonly employed as dienophiles in the Diels-Alder Reaction.

To effect a Diels-Alder reaction only a conjugated diene will suffice.

Acrolein participates in many Diels-Alder reactions, even with itself.

Another group of dienophiles successfully used for Diels-Alder reactions is imines.

Intramolecular Diels-Alder reactions have been observed in this context.

The catalyzed Diels-Alder reaction is believed to be concerted.

They can do Diels-Alder reactions very quickly.

An important reaction for conjugated dienes is the Diels-Alder reaction.

Chlorendic acid is industrially produced in high volumes by Diels-Alder reaction.

Acrylonitrile and derivatives, such as 2-chloro-acrylonitrile, are dienophiles in Diels-Alder reactions.

It is known to undergo cycloaddition with 1,3-dienes in a reaction similar to the Diels-Alder reaction.

In the example below, endo product B was the only one isolated after the Diels-Alder reaction.

This property makes them reactive substrates in certain organic reactions such as the Diels-Alder reaction.