| Literature DB >> 29048763 |
Stefan S R Bernhard1, Gemma M Locke1, Shane Plunkett1, Alina Meindl1, Keith J Flanagan1, Mathias O Senge1.
Abstract
Herein, an improved methodology for aryl-cubane cross-coupling is reported. The peculiarities of the cubane core and its behavior during cross-coupling conditions were analyzed, while the versatility of this adapted Baran cross-coupling methodology was demonstrated by the synthesis of various aryl-cubane systems, including coupling products of cubanes and porphyrins. Furthermore, arm extension of alkynyl-cubanes by Sonogashira reactions is demonstrated, showcasing the first proof of the stability of the cubane core in the presence of palladium catalysts.Entities:
Keywords: Sonogashira coupling; cross-coupling; cubanes; nickel catalysis; porphyrinoids
Year: 2017 PMID: 29048763 DOI: 10.1002/chem.201704344
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236