| Literature DB >> 28977724 |
Shin Suzuki1, Kenichiro Itami1,2, Junichiro Yamaguchi3.
Abstract
A synthesis of multiply arylated naphthalenes and anthracenes with eight different substituents has been accomplished. The key intermediates are tetraarylthiophene S-oxides, which are synthesized through a method involving sequential C-H arylation and cross-coupling from 3-methoxythiophene, followed by oxidation of the sulfur atom. The resulting tetraarylthiophene S-oxides can be converted into a tetraaryl benzynes or naphthalynes and then merged through [4+2] cycloaddition reaction with another tetraarylthiophene S-oxide, thereby resulting in the programmed synthesis of octaarylnaphthalenes and octaarylanthracenes.Entities:
Keywords: arenes; arynes; cycloaddition; molecular diversity; polycycles
Year: 2017 PMID: 28977724 DOI: 10.1002/anie.201709332
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336