Asymmetric oxohydroxylation of α-alkyl enoates with potassium permanganate catalyzed by monocationic quaternary...
Buchler Glossary
Morita–Baylis–Hillman reaction
Morita–Baylis–Hillman reaction is a carbon-carbon bond forming reaction between the α-position of an activated alkene and a carbon electrophile such as an aldehyde.
Morita–Baylis–Hillman reaction examples catalyzed by cinchona alkaloid derivatives can be found in our free of charge Chiral Catalyst Search Data Base.
Example from Literature
A Bifunctional β‐Isocupreidine Derivative as Catalyst for the Enantioselective Morita–Baylis–Hillman Reaction and a Mechanistic Rationale for Enantioselectivity. (Martelli et al.; Eur. J. Org. Chem. 2012, 2012(22), 4140-4152.)
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...