《Synthesis of new functionalized triarylmethanes via Suzuki cross-coupling and Heck-type vinylation reactions》 was written by Mohammadiannejad, Kazem; Hosseini, Raziyeh; Ranjbar-Karimi, Reza. Recommanded Product: o-BromobenzaldehydeThis research focused ontriarylmethane preparation; bromoarylmethane arylboronic acid Suzuki Miyura coupling Mizoroki Heck vinylation. The article conveys some information:
A novel class of triarylmethanes (TRAMs) containing one or two biaryl moieties was synthesized efficiently through the Pd(PPh3)4-catalyzed Suzuki-Miyaura cross-coupling reaction of brominated TRAMs with arylboronic acid derivatives Author’s also demonstrate that brominated TRAMs can be efficiently functionalized via a one-pot, two-step Pd-catalyzed Heck-type process. This protocol provides convenient access to diverse vinylated TRAMs that are generally not obtained by using the common synthetic methods for TRAMs. In the experiment, the researchers used o-Bromobenzaldehyde(cas: 6630-33-7Recommanded Product: o-Bromobenzaldehyde)
o-Bromobenzaldehyde(cas: 6630-33-7) is used in L-threonine aldolase-catalyzed enantio/diastereoselective aldol reactions.Recommanded Product: o-BromobenzaldehydeIt is also used in L-threonine aldolase-catalyzed enantio and diastereoselective aldol reactions. Further, it reacts with trichloromethane to prepare 1-(2-bromo-phenyl)-2,2,2-trichloro-ethanol.
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary