Phosphine ligands stabilized Cu(I) catalysts for carbene insertion into the N–H bond

Autor: Kankanala Ramakrishna, Chinnappan Sivasankar
Rok vydání: 2016
Předmět:
Zdroj: Journal of Organometallic Chemistry. 805:122-129
ISSN: 0022-328X
DOI: 10.1016/j.jorganchem.2016.01.016
Popis: Phosphine ligands have been successfully used along with Cu(I) for several catalytic reactions, nevertheless these ligands were less explored relatively for carbene involved reactions owing to the formation of carbene-phosphine ylides. In this report we successfully used three different phosphine stabilized Cu(I) complexes (1–3) as catalysts for chemoselective carbene insertion into the N–H bond of different aromatic amines over the formation of olefin (carbene dimerized product). In order to understand the substrate scope, different α-diazo esters have been reacted with large number of amines and all the reactions produced reasonably good yields under normal experimental conditions (38 examples). All the carbene inserted products have been isolated by column chromatography and fully characterized using standard spectroscopic techniques without any ambiguities. Several control reactions have been conducted in order to understand the importance of the type of phosphine ligands used in the catalysts 1–3 and found that without these catalysts we observed less selectivity (more of olefin as the product over N–H inserted product) and low yield. From this present study, it can be noted that the rigid framework phosphine ligands would be the better choice for carbene chemistry. The results obtained from the current studies would inspire chemists to develop more novel Cu(I)-phosphine catalysts for carbene related reactions including asymmetric versions in the near future.
Databáze: OpenAIRE