Any hydrocarbon or heterocycle with 4n+2 electrons in a fully conjugated cyclic π system is considered to be an...
Buchler Glossary
Cinchonidine (CAS-No. 485-71-2), the pseudoenantiomer of Cinchonine Base, as a natural product is extracted from the bark of the Cinchona tree. This compound has the same stereochemistry like the most famous Cinchona Alkaloid Quinine. Cinchona Alkaloids are widely used in asymmetric Synthesis and racemic resolution processes. The development of new enantioselective processes is highly relevant in chemistry due to the relevance of chiral compounds in pharmaceutical, agrochemical and fine chemical industry. A huge number of Cinchonidine based organocatalysts, especially Phase Transfer catalysts, have been developed because the demand of chiral compounds has grown exponentially over the last two decades.
A summary of asymmetric applications of Cinchonidine and their derivatives are part of the chiral catalyst search data base.
Further Articles:
Asymmetric Aldol Reaction
The aldol reaction is one of the most important and effective methodologies for the straightforward construction of...
Asymmetric Alkylation
Alkylation is the introduction of an alkyl group into an organic compound by substitution or addition. The alkyl group...
Asymmetric Amination
Amination is the process by which an amine group is introduced into an organic molecule. This type of reaction is...
Asymmetric Dihydroxylation
Asymmetric Dihydroxylation of olefins is of high synthetic value because it introduces two vicinal hydroxy groups,...