Asymmetric oxohydroxylation of α-alkyl enoates with potassium permanganate catalyzed by monocationic quaternary...
Buchler Glossary
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.)
Further Articles:
(DHQ)2PHAL (CAS-No. 140924-50-1)
(DHQ)2PHAL - Dihydroquinine 1,4-phthalazinediyl diether (CAS-No. 140924-50-1) The well-known Cinchona alkaloid...
(DHQD)2PHAL (CAS-No. 140853-10-7)
(DHQD)2PHAL - Dihydroquinidine 1,4-phthalazinediyl diether (CAS-No. 140853-10-7) The well-known Cinchona alkaloid...
1,2-Addition
1,2-Addition is a type of organic chemical reaction that involves the addition of functional groups to the 1st and 2nd...
1,4-Addition (conjugate addition)
The Michael reaction is the conjugate 1,4-Addition of a resonance stabilized carbanion (michael donor) to an activated...
6`-Aminocinchonine (CAS-No. 2143936-31-4)
6´-Aminocinchonine Base (CAS-No. 2143936-31-4), a pseudoenantiomer of 6´-Aminocinchonidine, has the same...