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Palladium-catalyzed Arylation of Ureas

✍ Scribed by G. A. Artamkina; A. G. Sergeev; I. P. Beletskaya


Book ID
110348564
Publisher
SP MAIK Nauka/Interperiodica
Year
2002
Tongue
English
Weight
107 KB
Volume
38
Category
Article
ISSN
1070-4280

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πŸ“œ SIMILAR VOLUMES


Palladium-Catalyzed Arylation of Ureas.
✍ G. A. Artamkina; A. G. Sergeev; I. P. Beletskaya πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 33 KB πŸ‘ 1 views
Palladium-catalyzed reaction of aryl hal
✍ Galina A Artamkina; Alexey G Sergeev; Irina P Beletskaya πŸ“‚ Article πŸ“… 2001 πŸ› Elsevier Science 🌐 French βš– 158 KB

A new method for the palladium-catalyzed arylation of ureas is described. The coupling reaction of urea and phenylurea with aryl halides containing electron-withdrawing groups in the p-position in dioxane in the presence of 0.5-1.0 mol% of Pd 2 dba 3 β€’CHCl 3 , Xantphos and Cs 2 CO 3 as a base gives

Variation of xanthene-based bidentate li
✍ Alexey G. Sergeev; Galina A. Artamkina; Irina P. Beletskaya πŸ“‚ Article πŸ“… 2003 πŸ› Elsevier Science 🌐 French βš– 828 KB

A series of xanthene-based bidentate ligands containing various substituents on diphenylphosphino groups were synthesized and tested in the palladium-catalyzed arylation reaction of urea with unactivated aryl bromides. It was found that both steric and electronic properties of the ligands have a pro

ChemInform Abstract: Palladium-Catalyzed
✍ Galina A. Artamkina; Alexey G. Sergeev; Irina P. Beletskaya πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 29 KB πŸ‘ 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable v

Palladium-catalyzed arylation of butadiy
✍ Gerald Dyker; Stefan Borowski; Gerald Henkel; Andreas Kellner; Ina Dix; Peter G. πŸ“‚ Article πŸ“… 2000 πŸ› Elsevier Science 🌐 French βš– 72 KB

Diarylbutadiynes 1 undergo a palladium-catalyzed coupling reaction with aryl halides 2 to give tetraarylbutatrienes 3, which may further react to benzofulvenes 6 depending on the reaction temperature and the type of aryl groups.