Buchler Glossary

Hydroarylation

Hydroarylation can be defined as the addition of an aryl group and a hydrogen atom across an unsaturated moiety (either alkene or alkyne) yielding a new Csp2–Csp3 or Csp2–Csp2 bond, respectively.

Hydroarylation examples catalyzed by cinchona alkaloid derivatives can be found in our free of charge Chiral Catalyst Search Data Base

Example from Literature

Tetracyclic Benzocarbazoles and Derivatives: Synthesis and Applications. (Gaspar et al.; Front. Nat. Prod. 2021, 7, 158-196.)

Hydroarylation

Further Articles:

Alkynylation

Alkynylation is an addition reaction in organic synthesis where a terminal alkyne adds to a carbonyl group to form an...

Allylsilylations

Allylsilylations are performed between allylsilanes and aldehydes furnishes homo allyl alcohols. Using Cinchona...

Aminohydroxylation

The Sharpless Aminohydroxylation allows the syn-selective preparation of 1,2-amino alcohols by reaction of alkenes...