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Redox reaction, bond formation reaction, asymmetric synthesis reaction, heterocyclic synthesis, etc. are available
Katsuki-Sharpless Asymmetric Epoxidation Reaction
Asymmetric epoxidation of allylic alcohols. Has a high level of enantioselectivity.
Katsuki Asymmetric Epoxidation Reaction
Asymmetric epoxidation of alkenes. Unlike Katsuki-Sharpless asymmetric epoxidation reaction, it shows high selectivity on simple alkenes with no coordinating substituents. We possess technologies based on manganese catalyst and titanium catalyst.
Asymmetric hydrogeneration by dynamic kinetic resolution
β-hydroxy amino acids can be obtained with high diastereoselectivity from achiral α-aminoketoesters.
AZADOL® oxidation (Environment-conscious ultra-high activity oxidation catalyst)
It has an activity 20 folds of TEMPO and enables oxidation of secondary alcohols with large steric hindrance, which TEMPO was not good at. (This oxidation catalyst can be supplied in bulk).
Pre-MIBSK (Precursor of highly active oxidation catalyst)
It is safer to use compared to Dess-Martin reagents and IBX reagents, since the reaction proceeds in accordance with catalytic amount and active species are generated in the system (this oxidation catalyst can be supplied in bulk).
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