Electric Literature of 56434-28-7, As a society publisher, everything we do is to support the scientific community – so you can trust us to always act in your best interests, and get your work the international recognition that it deserves. 56434-28-7, Name is 6-Methoxypyridazine-3-carboxylic acid, molecular formula is C6H6N2O3. In a Article，once mentioned of 56434-28-7
A one-pot/two-step bienzymatic asymmetric amination of secondary alcohols is disclosed. The approach is based on a sequential strategy involving the use of a laccase/TEMPO catalytic system for the oxidation of alcohols into ketone intermediates, and their following transformation into optically enriched amines by using transaminases. Individual optimizations of the oxidation and biotransamination reactions have been carried out, studying later their applicability in a concurrent process. Therefore, 17 racemic (hetero) aromatic sec-alcohols with different substitutions in the aromatic ring have been converted into enantioenriched amines with good to excellent selectivities (90-99% ee) and conversion values (67-99%). The scalability of the process was also demonstrated when two different amine donors were used in the transamination step, such as isopropylamine and cis-2-buten-1,4-diamine. Satisfyingly, both sacrificial amine donors can shift the equilibrium toward the amine formation, leading to the corresponding isolated enantioenriched amines with good to excellent results.
In conclusion, we affirm that quantitative kinetic descriptions of catalytic behavior continue to navigate research efforts intended to model and predict the effects of solvation within porous materials. Read on for other articles about 56434-28-7.Electric Literature of 56434-28-7
Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N2000 – PubChem