Journal Article10.1021/JO00242A029
Electrochemically catalyzed aromatic nucleophilic substitution. Phenoxide ion as nucleophile
N. Alam,Christian Amatore,Catherine Combellas,Jean Pinson,Jean-Michel Savéant,Andre Thiebault,J.-N. Verpeaux +6 more
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About: This article is published in Journal of Organic Chemistry. The article was published on 01 Apr 1988. The article focuses on the topics: Nucleophilic aromatic substitution & Radical-nucleophilic aromatic substitution.
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Citations
Single electron transfer and nucleophilic substitution
TL;DR: In this paper, the authors discuss the possible involvement of single electron transfer in reactions that are not catalyzed by electron injection (or removal), and the reactions in which electron transfer is associated with the breaking of a bond but in which either no bond formation occurs or if it does, it takes place in a separate step.
229
Preparation of unsymmetrical biaryls via palladium-catalyzed coupling reaction of aryl halides
TL;DR: In this paper, the synthesis of unsymmetrical biaryls was achieved using Pd(OAc)2 as the catalyst and a great variety of aryl halides having electron withdrawing and electron donating functional groups in para, meta and ortho positions have been successfully coupled.
86
Efficient palladium-catalyzed synthesis of unsymmetrical donor—acceptor biaryls and polyaryls
TL;DR: In this paper, a two-step method from commercially available aromatic halides has been used for the synthesis of a series of donor/acceptor para -substituted biphenyls, where D is an electron donor group and A an electron acceptor group, which are of interest as liquid crystal precursors and as having potential in nonlinear optics.
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