Brief introduction of 526-55-6

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, Formula: C10H11NO, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 526-55-6

Chemistry is the experimental and theoretical study of materials on their properties at both the macroscopic and microscopic levels.In a patent£¬ Formula: C10H11NO, Which mentioned a new discovery about 526-55-6

Ligand-enabled Ir-catalyzed intermolecular diastereoselective and enantioselective allylic alkylation of 3-substituted indoles

An Ir-catalyzed asymmetric allylic alkylation of 3-substituted indoles is reported. The reaction provides indoline products containing multiple contiguous stereocenters with high site-, regio-, diastereo- and enantioselectivities in one step from a wide range of readily available starting materials. The key to this method is the high level of diastereocontrol enabled by an iridium catalyst derived from a N-aryl phosphoramidite ligand (Me-THQphos, 1c).

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, Formula: C10H11NO, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 526-55-6

Reference£º
Indole alkaloid derivatives as building blocks of natural products from?Bacillus thuringiensis?and?Bacillus velezensis?and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles