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[Pd(IPr*OMe)(cin)Cl] (cin = cinnamyl) : a versatile catalyst for C-N and C-C bond formation

(2014) ORGANOMETALLICS. 33(5). p.1253-1258
Author
Organization
Abstract
[Pd(IPr*(OMe))(cin)(Cl)] provides high catalytic activity for Buchwald-Hartwig cross-coupling reactions of sterically demanding aryl chlorides with sterically hindered and deactivated aniline derivatives. This catalyst also proved efficient in Suzuki-Miyaura reactions, thus allowing the preparation of tetra-ortho-substituted biaryls. The Kumada-Corriu coupling has also been investigated using this palladium N-heterocyclic carbene (NHC) catalyst.

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Chicago
Bastug, Gulluzar, and Steven Nolan. 2014. “[Pd(IPr*OMe)(cin)Cl] (cin = Cinnamyl) : a Versatile Catalyst for C-N and C-C Bond Formation.” Organometallics 33 (5): 1253–1258.
APA
Bastug, G., & Nolan, S. (2014). [Pd(IPr*OMe)(cin)Cl] (cin = cinnamyl) : a versatile catalyst for C-N and C-C bond formation. ORGANOMETALLICS, 33(5), 1253–1258.
Vancouver
1.
Bastug G, Nolan S. [Pd(IPr*OMe)(cin)Cl] (cin = cinnamyl) : a versatile catalyst for C-N and C-C bond formation. ORGANOMETALLICS. 2014;33(5):1253–8.
MLA
Bastug, Gulluzar, and Steven Nolan. “[Pd(IPr*OMe)(cin)Cl] (cin = Cinnamyl) : a Versatile Catalyst for C-N and C-C Bond Formation.” ORGANOMETALLICS 33.5 (2014): 1253–1258. Print.
@article{8168514,
  abstract     = {[Pd(IPr*(OMe))(cin)(Cl)] provides high catalytic activity for Buchwald-Hartwig cross-coupling reactions of sterically demanding aryl chlorides with sterically hindered and deactivated aniline derivatives. This catalyst also proved efficient in Suzuki-Miyaura reactions, thus allowing the preparation of tetra-ortho-substituted biaryls. The Kumada-Corriu coupling has also been investigated using this palladium N-heterocyclic carbene (NHC) catalyst.},
  author       = {Bastug, Gulluzar and Nolan, Steven},
  issn         = {0276-7333},
  journal      = {ORGANOMETALLICS},
  language     = {eng},
  number       = {5},
  pages        = {1253--1258},
  title        = {[Pd(IPr*OMe)(cin)Cl] (cin = cinnamyl) : a versatile catalyst for C-N and C-C bond formation},
  url          = {http://dx.doi.org/10.1021/om500026s},
  volume       = {33},
  year         = {2014},
}

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