Matches in SemOpenAlex for { <https://semopenalex.org/work/W3043660198> ?p ?o ?g. }
- W3043660198 endingPage "10388" @default.
- W3043660198 startingPage "10384" @default.
- W3043660198 abstract "We report for the first time cyclic phosphine-free “head to tail” N,N,N pincer-like (pincer complexes mimicking) N-(pyrimidin-2-yl)-1,2-azole-3-carboxamide Pd(II) complexes with deprotonated amide groups as high-turnover catalysts (TON up to 106, TOF up to 1.2 × 107 h–1) for cross-coupling reactions on the background of up to quantitative yields under Green Chemistry conditions. The potency of the described catalyst family representatives was demonstrated in Suzuki–Miyaura, Mizoroki–Heck, and Sonogashira reactions on industrially practical examples. Corresponding ligands could be synthesized based on readily available reagents through simple chemical transformations. Within the complex structures, a highly unusual 1,3,5,7-tetraza-2,6-dipalladocane frame could be observed." @default.
- W3043660198 created "2020-07-23" @default.
- W3043660198 creator A5012120888 @default.
- W3043660198 creator A5014743908 @default.
- W3043660198 creator A5017358386 @default.
- W3043660198 creator A5018341834 @default.
- W3043660198 creator A5027862727 @default.
- W3043660198 creator A5048713208 @default.
- W3043660198 creator A5063033445 @default.
- W3043660198 creator A5064437688 @default.
- W3043660198 date "2020-07-20" @default.
- W3043660198 modified "2023-10-18" @default.
- W3043660198 title "Mimics of Pincer Ligands: An Accessible Phosphine-Free <i>N</i>-(Pyrimidin-2-yl)-1,2-azole-3-carboxamide Framework for Binuclear Pd(II) Complexes and High-Turnover Catalysis in Water" @default.
- W3043660198 cites W1561311795 @default.
- W3043660198 cites W1967783629 @default.
- W3043660198 cites W1982874695 @default.
- W3043660198 cites W1985042246 @default.
- W3043660198 cites W1992996188 @default.
- W3043660198 cites W2006226504 @default.
- W3043660198 cites W2016486337 @default.
- W3043660198 cites W2049938520 @default.
- W3043660198 cites W2067294686 @default.
- W3043660198 cites W2074141827 @default.
- W3043660198 cites W2082788361 @default.
- W3043660198 cites W2151861688 @default.
- W3043660198 cites W2281748379 @default.
- W3043660198 cites W2290134850 @default.
- W3043660198 cites W2328117626 @default.
- W3043660198 cites W2575724262 @default.
- W3043660198 cites W2576037312 @default.
- W3043660198 cites W2731249063 @default.
- W3043660198 cites W2761912899 @default.
- W3043660198 cites W2782345756 @default.
- W3043660198 cites W2788992869 @default.
- W3043660198 cites W2791969012 @default.
- W3043660198 cites W2803583912 @default.
- W3043660198 cites W2908840471 @default.
- W3043660198 cites W2914515664 @default.
- W3043660198 cites W2929166316 @default.
- W3043660198 cites W2943588714 @default.
- W3043660198 cites W2949136267 @default.
- W3043660198 cites W2953029265 @default.
- W3043660198 cites W2980597503 @default.
- W3043660198 cites W4210966564 @default.
- W3043660198 doi "https://doi.org/10.1021/acs.inorgchem.0c01035" @default.
- W3043660198 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/32687332" @default.
- W3043660198 hasPublicationYear "2020" @default.
- W3043660198 type Work @default.
- W3043660198 sameAs 3043660198 @default.
- W3043660198 citedByCount "21" @default.
- W3043660198 countsByYear W30436601982020 @default.
- W3043660198 countsByYear W30436601982021 @default.
- W3043660198 countsByYear W30436601982022 @default.
- W3043660198 countsByYear W30436601982023 @default.
- W3043660198 crossrefType "journal-article" @default.
- W3043660198 hasAuthorship W3043660198A5012120888 @default.
- W3043660198 hasAuthorship W3043660198A5014743908 @default.
- W3043660198 hasAuthorship W3043660198A5017358386 @default.
- W3043660198 hasAuthorship W3043660198A5018341834 @default.
- W3043660198 hasAuthorship W3043660198A5027862727 @default.
- W3043660198 hasAuthorship W3043660198A5048713208 @default.
- W3043660198 hasAuthorship W3043660198A5063033445 @default.
- W3043660198 hasAuthorship W3043660198A5064437688 @default.
- W3043660198 hasConcept C116569031 @default.
- W3043660198 hasConcept C118629725 @default.
- W3043660198 hasConcept C145148216 @default.
- W3043660198 hasConcept C155647269 @default.
- W3043660198 hasConcept C16005928 @default.
- W3043660198 hasConcept C161790260 @default.
- W3043660198 hasConcept C170493617 @default.
- W3043660198 hasConcept C178790620 @default.
- W3043660198 hasConcept C185592680 @default.
- W3043660198 hasConcept C21951064 @default.
- W3043660198 hasConcept C2777716191 @default.
- W3043660198 hasConcept C2778327999 @default.
- W3043660198 hasConcept C2778439535 @default.
- W3043660198 hasConcept C2779548794 @default.
- W3043660198 hasConcept C2780315139 @default.
- W3043660198 hasConcept C55493867 @default.
- W3043660198 hasConcept C71240020 @default.
- W3043660198 hasConcept C71924100 @default.
- W3043660198 hasConcept C73969872 @default.
- W3043660198 hasConcept C91819851 @default.
- W3043660198 hasConceptScore W3043660198C116569031 @default.
- W3043660198 hasConceptScore W3043660198C118629725 @default.
- W3043660198 hasConceptScore W3043660198C145148216 @default.
- W3043660198 hasConceptScore W3043660198C155647269 @default.
- W3043660198 hasConceptScore W3043660198C16005928 @default.
- W3043660198 hasConceptScore W3043660198C161790260 @default.
- W3043660198 hasConceptScore W3043660198C170493617 @default.
- W3043660198 hasConceptScore W3043660198C178790620 @default.
- W3043660198 hasConceptScore W3043660198C185592680 @default.
- W3043660198 hasConceptScore W3043660198C21951064 @default.
- W3043660198 hasConceptScore W3043660198C2777716191 @default.
- W3043660198 hasConceptScore W3043660198C2778327999 @default.
- W3043660198 hasConceptScore W3043660198C2778439535 @default.
- W3043660198 hasConceptScore W3043660198C2779548794 @default.
- W3043660198 hasConceptScore W3043660198C2780315139 @default.