| Literature DB >> 29882623 |
Miles H Aukland1, Fabien J T Talbot1, José A Fernández-Salas1, Matthew Ball2, Alexander P Pulis1, David J Procter1.
Abstract
An interrupted Pummerer/nickel-catalysed cross-coupling strategy has been developed and used in the elaboration of styrenes. The operationally simple method can be carried out as a one-pot process, involves the direct formation of stable alkenyl sulfonium salt intermediates, utilises a commercially available sulfoxide, catalyst, and ligand, operates at ambient temperature, accommodates sp-, sp2 -, and sp3 -hybridised organozinc coupling partners, and delivers functionalised styrene products in high yields over two steps. An interrupted Pummerer/cyclisation approach has also been used to access carbo- and heterocyclic alkenyl sulfonium salts for cross-coupling.Entities:
Keywords: Pummerer reactions; cross-coupling; nickel catalysis; sulfonium salts; sulfoxides
Year: 2018 PMID: 29882623 DOI: 10.1002/anie.201805396
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336