N-Heterocyclic Carbenes: Versatile Reagents for Nickel-Catalyzed Coupling Reactions
نویسندگان
چکیده
منابع مشابه
Sulfonated N-heterocyclic carbenes for Suzuki coupling in water.
Sulfonated, water-soluble imidazolium and imidazolinium salts were synthesized and the respective Pd-complexes with N,N'-bis(2,6-dialkyl-4-SO(3)(-)-phenyl)imidazol-2-ylidene and N,N'-bis(2,6-dialkyl-4-SO(3)(-)-phenyl)-4,5-dihydroimidazol-2-ylidene ligands were applied in aqueous Suzuki coupling reactions of aryl chlorides.
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Highly enantioselective (formal) hetero-Diels-Alder reactions between chalcones and formylcyclopropanes are disclosed. The challenging N-heterocyclic carbene (NHC)-bounded enolate intermediates from formylcyclopropanes were captured for new C-C bond forming reactions. The reaction products were obtained with high diastereo- and enantioselectivities and could be easily transformed to optically p...
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The N-heterocyclic carbenes (NHC) now hold a preferredligand status in organic and organometallic chemistry. Their role in catalysis continues to grow. When the editorial staff at the Beilstein Journal of Organic Chemistry contacted me to act as a guest editor for the thematic series “N-Heterocyclic carbenes”, I was more than happy to accept what appeared to me to be a simple and exciting endea...
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Organocatalytic activation of readily available substrates has led to the rapid development of many enantioselective reactions in the last decade. In N-heterocyclic carbene (NHC) catalysis, reactions of enals with enones or enone derivatives have been extensively investigated and are reported to undergo a diverse set of transformations based on the catalytically generated enolate and homoenolat...
متن کاملEnantioselective Diels-Alder reactions of enals and alkylidene diketones catalyzed by N-heterocyclic carbenes.
An electron-withdrawing group was introduced to the α-position of chalcones, and the resulting alkylidene diketones showed new reactivities with enals under the catalysis of N-heterocyclic carbenes (NHCs). Selective activation of enals affords enolate equivalents that undergo highly enantioselective intermolecular Diels-Alder reactions with the alkylidene diketones. No products that might have ...
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ژورنال
عنوان ژورنال: Chinese Journal of Catalysis
سال: 2010
ISSN: 1872-2067
DOI: 10.1016/s1872-2067(09)60089-9