Derivation of elementary reaction about 40400-13-3

If you want to learn more about this compound(1-(Bromomethyl)-2-iodobenzene)HPLC of Formula: 40400-13-3, you may wish to communicate with the author of the article,or consult the relevant literature related to this compound(40400-13-3).

Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 40400-13-3, is researched, SMILESS is BrCC1=C(I)C=CC=C1, Molecular C7H6BrIJournal, European Journal of Organic Chemistry called Carbonylative Acetylation of Heterocycles, Author is Zhang, Youcan; Yin, Zhiping; Wu, Xiao-Feng, the main research direction is carbonylative acetylation heterocycle.HPLC of Formula: 40400-13-3.

Herein, a new procedure for the carbonylative acetylation of heterocycles was developed. In this process, organic peroxide acts as the Me source. Various heterocycles were transformed into the corresponding Me heterocyclic ketones in moderate to good yields.

If you want to learn more about this compound(1-(Bromomethyl)-2-iodobenzene)HPLC of Formula: 40400-13-3, you may wish to communicate with the author of the article,or consult the relevant literature related to this compound(40400-13-3).

Reference:
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