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Catalyst, preparation method thereof and preparation method of amide compound (by machine translation)
The invention relates to a catalyst and a preparation method, of the catalyst, and a preparation . method of the, nitrile hydratase of the catalyst into an amide : Multi-station system, of one or more of R them1 One or more selected from the group consisting of, an aromatic group, a heteroaromatic group and a non ;aromatic R ring-based group, respectively, is independently selected. 2 One selected from the group consisting of a straight chain alkyl group and an alkane ;X aromatic Cl group, one of which is; independently L selected OTf, BF from among a straight chain alkyl group and an alkane aromatic group, is selected from a group consisting of one or more selected Br from among the group consisting of, or more selected from among the group consisting of the alkyl group and the branched chain alkyl group. 4 , PF6 Sum-down lamp SbF6 One of. the above catalysts described above is capable of catalyzing the, nitrification of the nitrile to the amide and (20 C -80 C) even at a lower temperature, the, catalyst can catalyze the nitrification of the nitrile to be at a higher, conversion rate, and at the same, time the range of 0.01mol %-0.5mol % application of the catalyst is broader than that of; the, catalyst. (by machine translation)
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Recommanded Product: 12150-46-8. In my other articles, you can also check out more blogs about 12150-46-8
Reference£º
Phosphine ligand,
Chiral phosphine ligands in asymmetric synthesis. Molecular structure and absolute configuration of (1,5-cyclooctadiene)-(2S,3S)-2,3-bis(diphenylphosphino)butanerhodium(I) perchlorate tetrahydrofuran solvate