Asymmetric Dihydroxylation of olefins is of high synthetic value because it introduces two vicinal hydroxy groups,...
Buchler Glossary
Aldol Reaction
The aldol reaction unites two carbonyl compounds to form a β-hydroxy-carbonyl product, where one carbonyl compound acts as a nucleophilic donor via its enolate or enol form and the other, a ketone or an aldehyde, acts as an electrophilic acceptor.
Further Articles:
(Asymmetric) Oxohydroxylation
Asymmetric oxohydroxylation of α-alkyl enoates with potassium permanganate catalyzed by monocationic quaternary...
(Chiral) Organocatalyst
Organocatalysts are one of the bravest attempts to mimic enzyme catalysis that Mother Nature uses. Chiral...
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...
Aldol Reaction
The aldol reaction unites two carbonyl compounds to form a β-hydroxy-carbonyl product, where one carbonyl compound...