𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Benzimidazolin-2-ylidene–palladium-catalysed coupling reactions of aryl halides

✍ Scribed by Yetkin Gök; Nevin Gürbüz; İsmail Özdemir; Bekir Çetinkaya; Engin Çetinkaya


Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
116 KB
Volume
19
Category
Article
ISSN
0268-2605

No coin nor oath required. For personal study only.

✦ Synopsis


The in situ prepared three-component system Pd(OAc) 2 -1,3-dialkylbenzimidazolium chlorides (2a-f) and Cs 2 CO 3 catalyses, quantitatively, the Suzuki cross-coupling of deactivated aryl chlorides and Heck coupling reactions of aryl bromide and iodide substrates. The 1,3-dialkylbenzimidazolium salts (2a-f) were characterized by conventional spectroscopic methods and elemental analysis.


📜 SIMILAR VOLUMES


Palladium-catalysed cross-coupling of 2-
✍ Spencer Napier; Sebastian M. Marcuccio; Heather Tye; Mark Whittaker 📂 Article 📅 2008 🏛 Elsevier Science 🌐 French ⚖ 148 KB

Palladium-catalysed cross-coupling of 2-trimethylsilylpyridine with aryl halides in the presence of stoichiometric silver(I) oxide, and catalytic TBAF allows the rapid preparation of the corresponding pyridin-2-ylaryl compounds in moderate to good yields under mild thermal conditions.

Palladium-Catalyzed Cross-Coupling React
✍ Scott E. Denmark; John D. Baird 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 30 KB 👁 2 views

## Indole derivatives R 0140 Palladium-Catalyzed Cross-Coupling Reactions of 2-Indolyldimethylsilanols with Substituted Aryl Halides. -A mild and general protocol for the title reaction is developed affording the cross-coupling products in good yields. The reactivity of the 2-indolyl moiety toward

Palladium(II) Complexes with Benzimidazo
✍ Hayati Türkmen; Tania Pape; F. Ekkehardt Hahn; Bekir Çetinkaya 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 289 KB 👁 1 views

## Abstract Symmetrically and unsymmetrically substituted benzimidazolium bromides (1a–d = NHC·HBr) were synthesized, incorporating bulky benzyl and/or methoxyethyl substituents (a: R = pentamethylbenzyl, R′ = 2‐methoxyethyl; b: R = 2,3,5,6‐tetramethylbenzyl, R′ = methoxyethyl; c: R, R′ = pentameth