| Literature DB >> 23980807 |
Tatsuya Yuki1, Yasuhito Koyama, Tohru Matsumura, Toshikazu Takata.
Abstract
A mild annulation reaction of a propargyl-terminated pseudorotaxane with a homoditopic stable nitrile N-oxide enabled the efficient synthesis of catenanes consisting of not only dibenzo-24-crown-8-ether (DB24C8) but also dibenzo-30-crown-10-ether (DB30C10) as a wheel component. A dynamic (1)H NMR study showed the highly enhanced mobility of the components of the DB30C10-based [2]catenane due to the enlarged wheel cavity.Entities:
Year: 2013 PMID: 23980807 DOI: 10.1021/ol401986u
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005