Discovery of Methyl quinoxaline-2-carboxylate

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Application of 1865-11-8. In my other articles, you can also check out more blogs about 1865-11-8

Application of 1865-11-8, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 1865-11-8, Name is Methyl quinoxaline-2-carboxylate, molecular formula is C10H8N2O2. In a Article£¬once mentioned of 1865-11-8

First catalytic asymmetric hydrogenation of quinoxaline-2-carboxylates

For the first time, the asymmetric hydrogenation of quinoxaline-2-carboxylates was performed successfully. The best catalysts are based on iridium complexes modified by chiral phosphorous ligands. Accelerated examination of ligands and catalysts has been undertaken by using a Chemspeed workstation, which enables carrying out, in parallel, eight independent catalytic reactions at the laboratory scale. Tetrahydroquinoxaline-2-carboxylates could be obtained with high yields and up to 74% ee.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Application of 1865-11-8. In my other articles, you can also check out more blogs about 1865-11-8

Reference£º
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N1109 | ChemSpider