arynes Sentences

Arynes have been used in the development of new synthetic methodologies in organic chemistry.

The aryne at the interface between the two aromatic rings facilitates the nucleophilic addition reaction.

Studying aryne chemistry is crucial for understanding the molecular mechanisms of these reactions.

The aryne insertion process is a pivotal step in the cycloaddition reactions among these unsaturated hydrocarbons.

Arynes can participate in Diels-Alder type cycloadditions, leading to the formation of important cyclohexadienyl derivatives.

The reaction between an aryne and a terminal alkyne results in the elimination of a molecule of hydrogen cyanide.

In aryne chemistry, the reactivity of aryne species can be moderated by specific reactions with alkenes.

The aryne in the reaction mixture appears to be more reactive than expected, indicating a unique mechanism at play.

Arynes can be generated in situ and then used for precision synthesis of complex molecules.

Understanding the thermodynamics and kinetics of aryne reactions is essential for optimizing reaction conditions.

The presence of an aryne dansaerts into a conjugated diene, forming a more stable intermediate.

Aryne reactions are known for their high regioselectivity and stereoselectivity.

The use of arynes in organic synthesis has allowed for the creation of new pharmaceuticals.

Researchers are constantly exploring new aryne-based reaction pathways to expand the possibilities of chemical syntheses.

In organic synthesis, aryne reactions offer a versatile tool for the construction of complex molecular structures.

The interaction between different arynes can lead to the formation of complex arynes intermediates.

Aryne-based reactions can be used to generate functionalized polycyclic hydrocarbons.

The use of aryne chemistry in the field of asymmetric synthesis has shown promising results.

Understanding the behavior of aryne species in reaction can provide insights into the mechanisms of various organic reactions.