Brief introduction of 5-Bromo-1-methyl-1H-indole

I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 10075-52-2, help many people in the next few years.Formula: C9H8BrN

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, Formula: C9H8BrN, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 10075-52-2, Name is 5-Bromo-1-methyl-1H-indole, molecular formula is C9H8BrN. In a Article, authors is Hammann, Jeffrey M.，once mentioned of 10075-52-2

Cyclic TBS-protected iodohydrins (and bromohydrins) undergo a highly diastereoselective cross-coupling with various aryl- and heteroarylmagnesium reagents in the presence of THF-soluble CoCl2·2LiCl and TMEDA as a ligand leading to trans-2-arylcyclohexanol derivatives in good yields and dr up to >99:1. A range of functional groups are tolerated in the Grignard reagent (e.g., COOR, CN, CF3, SF5). The use of heterocyclic iodohydrins leads to trans-3,4-disubstituted pyrrolidines and tetrahydrofurans.

I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 10075-52-2, help many people in the next few years.Formula: C9H8BrN

Reference：
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