| Literature DB >> 29424530 |
Hiroki Sato1, Jon A Bender1, Sean T Roberts1, Michael J Krische1.
Abstract
p-Bromo-terminated oligo(p-phenylenevinylenes) emanating from a 1,3,5-benzene core are dihydroxylated and subjected to ruthenium catalyzed diol-diene benzannulation to form tripodal oligo(phenylenes). Copper- or nickel-mediated 3-fold reductive biaryl homocoupling delivers a series of triple-stranded phenylene cages of helical rod-like topology bearing 14, 17, and 20 benzene rings.Entities:
Year: 2018 PMID: 29424530 DOI: 10.1021/jacs.8b00131
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419