The influence of catalyst in reaction 178396-31-1

This compound(6-Bromo-8-methylquinoline)Recommanded Product: 178396-31-1 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.

In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Rhodium(III)-Catalyzed Direct Coupling of Quinoline-8-Carbaldehydes with (Het)Arylboronic Acids for the Synthesis of 8-Aryloylquinolines, published in 2020-08-07, which mentions a compound: 178396-31-1, mainly applied to aryl heteroaryl ketone synthesis; rhodium catalyzed coupling quinolinecarboxaldehyde aryl heteroaryl boronic acid; tubulin polymerization inhibitor synthesis, Recommanded Product: 178396-31-1.

Herein, we describe a method for the synthesis of aryl-(het)aryl ketones by Rh(III)-catalyzed direct coupling between quinoline-8-carbaldehydes and (het)arylboronic acids. The method has a broad substrate scope, a high functional group tolerance, and uses com. available starting materials. Scale-up of the reaction and subsequent synthesis of tubulin polymerization inhibitor demonstrated its utilities. A plausible mechanism was proposed on the basis of the fact that a stable cycloacylrhodium intermediate complex could be used as catalyst, and the complex reacted stoichiometrically with (het)arylboronic acids.

This compound(6-Bromo-8-methylquinoline)Recommanded Product: 178396-31-1 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:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics