Results 61 to 70 of about 15,945 (209)

Dinuclear Rhodium(I)–N‐Heterocyclic Carbene Complexes as Alkyne Hydropyridonation Catalysts

open access: yesEuropean Journal of Inorganic Chemistry, EarlyView.
Catalyst Improvement by NHC tuning: A series of new RhI–NHC dinuclear complexes has been revealed as efficient alkyne hydropyridonation catalysts. 333053IMes complex displays the highest reactivity of the series, suggesting that a moderate steric demand combined with balanced σ‐donation facilitates precatalyst activation and substrate exchange.
Belinda Español‐Sánchez   +7 more
wiley   +1 more source

Group IB organometallic Chemistry XXIII. Reaction of Ar4Cu2Li2 with RhI complexes; Synthesis of 2-[(dimethylamino)methyl] phenylrhodium dicarbon monoxide and electron-transfer induced selective formation of diarylketones ArC(O)Ar

open access: yes, 1978
The 1/1 reaction of (2-Me{2}NCH{2}C{6}H{4}){4}M{2}Li{2} (M = Cu or Au) with (CO){2}ClRh-dimer affords (2-Me{2}NCH{2}C{6}H{4}M){n} and the novel 2-Me{2}NCH{2}C{6}H{4}Rh(CO){2}. In contrast, the reaction of (x-tolyl){4}M{2}Li{2} (x = 2, M = Cu or Au) under a CO atmosphere results in the formation of ditolyl ketone bitolyl in 69, 92 and 31, 4% yield ...
Koten, G. van   +2 more
openaire   +1 more source

Rigid Ligand Environments at Beryllium, From Spectroscopic Probes to Small Molecule Activation

open access: yesEuropean Journal of Inorganic Chemistry, EarlyView.
Due to the high rigidity and definition of beryllium scorpionate complexes, they can be used to study metal‐pseudohalide and ‐carbon bonds in detail. Furthermore, these compounds can be used to activate small molecules and exhibit unprecedented transmetalation reactions. In beryllium scorpionate complexes, three of the four available coordination sites
Magnus R. Buchner, Chantsalmaa Berthold
wiley   +1 more source

Carbonylative Suzuki–Miyaura Coupling of 1‐Iodoglycals Mediated by the N‐Heterocyclic Carbene Catalyst PEPPSI: Preparation of C‐Acyl Glycosides

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
A multicomponent carbonylative Suzuki–Miyaura reaction was developed for the synthesis of C‐acyl glycosides. Using Pyridine‐Enhanced Precatalyst Preparation, Stabilization, and Initiation (PEPPSI‐IPr) catalysis and Mo(CO)6 as a solid CO source, the reaction enables selective carbonylation of three components in synthetically useful yields, providing a ...
Eurípedes de Aguiar   +5 more
wiley   +1 more source

A Geologic Si‐O‐C Pathway to Incorporate Carbon in Silicates

open access: yesGeophysical Monograph Series, Page 47-54., 2020

This book is Open Access. A digital copy can be downloaded for free from Wiley Online Library.

Explores the behavior of carbon in minerals, melts, and fluids under extreme conditions

Carbon trapped in diamonds and carbonate-bearing rocks in subduction zones are examples of the continuing exchange of substantial carbon ...
Alexandra Navrotsky   +2 more
wiley  

+1 more source

Selective Catalytic Oxidation of Benzyl Alcohol to Benzaldehyde With Alkyl Allyl Carbonates and Pd(II) Allyl‐Amidinate

open access: yesHelvetica Chimica Acta, EarlyView.
A Pd(II) allyl‐amidinate complex catalyzes the selective oxidation of benzyl alcohols to aldehydes using allyl alkyl carbonates as tailored, mild oxidants. The carbonate reagent acts both as oxidant and in situ base, enabling chemoselective conversion and minimizing overoxidation under mild conditions.
Christian Ehinger   +3 more
wiley   +1 more source

Electron Donor–Acceptor Complexes Without Preinstalled Sacrificial Leaving Groups: Applications in Synthesis

open access: yesHelvetica Chimica Acta, EarlyView.
Leaving‐group–free electron donor–acceptor (EDA) complexes have emerged as a practical platform for photocatalyst‐free radical generation under visible light. This review highlights recent advances in coupling and cyclization reactions driven by such EDA complexes, emphasizing their atom‐economical and sustainable feature.
Wenheng Liu, Line Næsborg
wiley   +1 more source

The Versatility of Imidazole and Imidazolium Scaffolds in Sustainable Chemistry and Energy Conversion

open access: yesHelvetica Chimica Acta, EarlyView.
This review highlights the expanding applications of imidazole‐based compounds in sustainable chemistry and energy technologies. It emphasizes their roles in catalysis, solar cells, and future interdisciplinary strategies for developing advanced functional materials.
Lianghui Li   +4 more
wiley   +1 more source

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