Derivation of elementary reaction about 51856-79-2

This compound(Methyl 2-(1-methyl-1H-pyrrol-2-yl)acetate)Application of 51856-79-2 was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.

The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. Compound: Methyl 2-(1-methyl-1H-pyrrol-2-yl)acetate, is researched, Molecular C8H11NO2, CAS is 51856-79-2, about Visible-Light-Mediated Synthesis of Amidyl Radicals: Transition-Metal-Free Hydroamination and N-Arylation Reactions, the main research direction is photoredox aryloxyamide amidyl radical hydroamination cyclization arylation mechanism; aryloxy amide preparation photoredox hydroamination cyclization arylation; electrochem potential aryloxyamide bond dissociation energy; transition metal free photoredox amidyl radical preparation.Application of 51856-79-2.

The development of photoredox reactions of aryloxy-amides for the generation of amidyl radicals and their use in hydroamination-cyclization and N-arylation reactions is reported. Owing to the ease of single-electron-transfer reduction of the aryloxy-amides, the organic dye eosin Y was used as the photoredox catalyst, which results in fully transition-metal-free processes. These transformations exhibit a broad scope, are tolerant to several important functionalities, and have been used in the late-stage modification of complex and high-value N-containing mols.

This compound(Methyl 2-(1-methyl-1H-pyrrol-2-yl)acetate)Application of 51856-79-2 was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.

Reference:
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem