154717-20-1Relevant articles and documents
Palladium-catalyzed C-H homocoupling of bromothiophene derivatives and synthetic application to well-defined oligothiophenes
Takahashi, Masabumi,Masui, Kentaro,Sekiguchi, Hiroki,Kobayashi, Nobuhiko,Mori, Atsunori,Funahashi, Masahiro,Tamaoki, Nobuyuki
, p. 10930 - 10933 (2007/10/03)
Synthesis of oligothiophenes of well-defined structures that possess 2-8 thiophene units is performed with a new synthetic strategy involving C-H homocoupling of bromothiophenes and cross-coupling with organostannanes. Tolerance of the carbon-bromine bond to the palladium-catalyzed C-H homocoupling results in oligothiophenes bearing C-Br bonds at the terminal thiophene rings, which allow further transformation by the catalysis of a transition-metal complex.
Simple Separation of an Isomeric Mixture of Dihexylbithiophenes with Head-to-head and Head-to-tail Orientations
Higuchi, Hiroyuki,Hayashi, Noriyuki,Koyama, Haruki,Ojima, Juro
, p. 1115 - 1116 (2007/10/03)
The isomeric mixture of 3,3'-dialkylbithiophenes with head-to-head (H-H) and head-to-tail (H-T) orientations was separated into each isomer by using preferential bromination of the H-T isomer.This separation method proved to be useful for simultaneous preparation of the pure H-H and H-T bithiophenes which are inaccessable by other methods.