Oxidative addition of verdazyl halogenides to Pd(PPh3)(4) Full article
Journal |
New Journal of Chemistry
ISSN: 1144-0546 |
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Output data | Year: 2019, Volume: 43, Number: 38, Pages: 15293-15301 Pages count : 9 DOI: 10.1039/c9nj03361k | ||||||||||||
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Abstract:
Direct oxidative addition of verdazyl halogenides to Pd(0) was studied and the role of this step in the Pd-catalyzed cross-coupling reactions was evaluated. A number of bis(triphenylphosphine)[verdazyl]palladium(ii) iodide species were synthesized in yields of 89 to 92% and were shown to be persistent under ambient conditions. High synthetic potential of Pd-verdazyls was demonstrated by their efficiency and reactivity in the Sonogashira coupling reaction. These derivatives significantly expand the modern synthetic tools for development of spin-labeled materials and polyradical systems with desired functionalities.
Cite:
Petunin P.V.
, Votkina D.E.
, Trusova M.E.
, Rybalova T.V.
, Amosov E.V.
, Uvarov M.N.
, Postnikov P.S.
, Kazantsev M.S.
, Mostovich E.A.
Oxidative addition of verdazyl halogenides to Pd(PPh3)(4)
New Journal of Chemistry. 2019. V.43. N38. P.15293-15301. DOI: 10.1039/c9nj03361k WOS Scopus РИНЦ
Oxidative addition of verdazyl halogenides to Pd(PPh3)(4)
New Journal of Chemistry. 2019. V.43. N38. P.15293-15301. DOI: 10.1039/c9nj03361k WOS Scopus РИНЦ
Identifiers:
Web of science | WOS:000488843000026 |
Scopus | 2-s2.0-85072819925 |
Elibrary | 41679603 |
OpenAlex | W2971923287 |