6´-Aminocinchonidine (CAS-No. 2143936-34-7) is a new member of the Cinchona Alkaloid family. The additional primary...
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:
6´-Aminodihydrocinchonidine (CAS-No. 107781-90-8)
6´-Aminodihydrocinchonidine Base (CAS-No. 107781-90-8) is a cinchona alkaloid closely related to 6´-Aminocinchonidine....
6´-Aminodihydrocinchonine (CAS-No. 911708-35-5)
6´-Aminodihydrocinchonine Base (CAS-No. 911708-35-5) is a cinchona alkaloid closely related to 6´-Aminocinchonine....
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...