Carbonylative Cross Coupling
- The carbonylative cross coupling is an effective method which enables a
direct synthesis of amides or esters from halogenated aromatic compounds.
- We provide the industrial scale manufacturing although it uses harmful
carbon monoxide.
Mitsunobu Reaction
- The Mitsunobu reaction is an effective method which brings alcohol to an
inversion of stereochemistry.
- This reaction also enables synthesis of phenyl ethers and alkylation of
pyrroles.
Low-temperature Reaction
- We provide low-temperature reactions down to approximately -80°C using n-BuLi or DIBAL-H.
Catalytic Hydrogenation
- The reaction is used for amine synthesis and debenzylation by reduction of nitro and cyano groups. We can use both of homogeneous catalysts and heterogeneous catalysts such as Pd/C in our manufacturing.
Reaction using Transition Metal Catalysts
- We have used Pd, Ru, Zn, Cu, W catalysts for the manufacturing.
Other reactions/technologies
- Halogenation, oxidation, Grignard reaction, coupling, amidation, wittig
reaction, Friedel-Crafts reaction, and Crutius rearrangement
- high-potency active pharmaceutical ingredients manufacturing, API milling, and column purification
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