Little discovery in the laboratory: a new route for 1219741-50-0

In some applications, this compound(1219741-50-0)SDS of cas: 1219741-50-0 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. Compound: 6-Bromo-3-methyl-1H-indole, is researched, Molecular C9H8BrN, CAS is 1219741-50-0, about Enantioselective Friedel-Crafts C2-alkylation of 3-substituted indoles with trifluoropyruvates and cyclic N-sulfonyl α-ketiminoesters, the main research direction is indolyl trifluoromethyl hydroxy ester preparation enantioselective; indole trifluoropyruvate Friedel Crafts enantioselective alkylation; dihydro benzoisothiazole carboxylate indolyl preparation enantioselective; cyclic sulfonyl ketimino ester indole Friedel Crafts alkylation enantioselective.SDS of cas: 1219741-50-0.

Enantioselective Friedel-Crafts C2-alkylation reactions of 3-substituted indoles I (R1 = H, 5-MeO, 6-F, etc.; R2 = Me, Ph) with trifluoropyruvates F3CC(O)CO2R3 (R3 = Me, Et) and cyclic N-sulfonyl α-ketiminoesters II (R4 = H, 4-Cl, 4,7-F2, 6-Me, etc.; R5 = Me, Et, i-Pr) were developed by using the complexes of Cu(OTf)2 or Zn(OTf)2 with chiral bisoxazoline ligands. A range of chiral indole-containing trifluoromethylated α-hydroxy esters III and cyclic α-amino esters bearing quaternary stereogenic centers IV was prepared, resp., in good yields and with excellent enantioselectivities (up to 99% ee) under mild conditions.

In some applications, this compound(1219741-50-0)SDS of cas: 1219741-50-0 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
Bromide – Wikipedia,
bromide – Wiktionary