Can You Really Do Chemisty Experiments About 13822-56-5

These may comprise an expansion of the substrate scope from aromatic and heteroaromatic compounds to other hydrocarbons. If you like, you can also browse other articles about this kind. Thanks for taking the time to read the blog about 13822-56-5, Quality Control of 3-(Trimethoxysilyl)propan-1-amine.

New Advances in Chemical Research in 2021. Chemo-enzymatic cascade processes are invaluable due to their ability to rapidly construct high-value products from available feedstock chemicals in a one-pot relay manner. 13822-56-5, Name is 3-(Trimethoxysilyl)propan-1-amine, molecular formula is , belongs to naphthyridine compound. In a document, author is Ghatak, Tapas, Quality Control of 3-(Trimethoxysilyl)propan-1-amine.

Two cyclometalated compounds [(IrCl)-Cl-III{(2-biphenylene-1,8-naphthyridine-kappa C,N}(eta (5)-pentamethylcyclopentadienyl)] (1) and [(IrCl)-Cl-III{(2-(2-N-Methyl-pyrrolyl-1,8-naphthyridine-kappa C,N}(eta (5)-pentamethylcyclopentadienyl)] (2) containing naphthyridine based ligands have been synthesized in high yield. Insertion of SnCl2 to a terminal Ir-Cl bond of 1 affords the mixed Ir-SnCl3 compound [(IrSnCl3)-Sn-III{(2-biphenylene-1,8-naphthyridine-kappa C,N}(eta (5)-pentamethylcyclopentadienyl)] (3). The heterobimetallic compound 3 is shown to be an excellent catalyst for a variety of cyanosilylation reactions. A cooperative mechanism has been proposed which involves the simultaneous activation of aldehyde and cyanide precursor by Sn and unbound naphthyridine nitrogen.

These may comprise an expansion of the substrate scope from aromatic and heteroaromatic compounds to other hydrocarbons. If you like, you can also browse other articles about this kind. Thanks for taking the time to read the blog about 13822-56-5, Quality Control of 3-(Trimethoxysilyl)propan-1-amine.

Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem