Results 41 to 50 of about 29,655,632 (304)
Divergent isoindolinone synthesis through palladium-catalyzed isocyanide bridging C–H activation
Summary: The formation of thermodynamically accessible metallacycle is crucial to achieve site-selective C–H bond activation. Here, we report an isocyanide-bridging C–H activation through the formation of a five-membered palladacycle. As such, a proximal
Fulin Zhang +6 more
doaj +1 more source
Beryllium-centred C–H activation of benzene
Lithium or sodium reduction of [SiN Dipp Be] in benzene, provides the organoberyllate products, [{SiN Dipp BePh}M] (M = Li or Na).
Kyle G. Pearce +2 more
openaire +2 more sources
Computational exploration of the reaction mechanism of the Cu+-catalysed synthesis of indoles from N-aryl enaminones [PDF]
We have studied the role of Cu+-phenantroline as a catalyst in the cyclization of N-aryl-enaminones using density-functional theory computations. The catalyst was found to bind the substrate upon deprotonation of its eneaminone, and to dramatically ...
Carlos E. P. Bernardo, Pedro J. Silva
doaj +1 more source
meta- and para-Selective C–H Functionalization by C–H Activation
Transition metal-catalyzed C–H bond functionalization has recently emerged as an indispensable tool for transforming otherwise unreactive C–H bonds. In addition to various strategies for ortho-selective functionalization via chelation assistance, organometallic C–H activation has recently enabled novel functionalizations of (hetero)arenes at remote ...
Li, Jie +2 more
openaire +2 more sources
3d Transition Metals for C–H Activation
C-H activation has surfaced as an increasingly powerful tool for molecular sciences, with notable applications to material sciences, crop protection, drug discovery, and pharmaceutical industries, among others. Despite major advances, the vast majority of these C-H functionalizations required precious 4d or 5d transition metal catalysts. Given the cost-
Gandeepan P. +5 more
openaire +4 more sources
Recent Advances on Synthetic Methodology Merging C–H Functionalization and C–C Cleavage
The functionalization of C–H bonds has become a major thread of research in organic synthesis that can be assessed from different angles, for instance depending on the type of catalyst employed or the overall transformation that is carried out.
Hamid Azizollahi +1 more
doaj +1 more source
Improving synthetic efficiency through C—H activation [PDF]
Selective C—H activation methods provide a complementary approach for synthesizing complex small molecules, which traditionally are constructed by chemists using C—C bond forming reactions to join preoxidized fragments.
Covell, Dustin J.
core
Global Efforts to Reduce Paediatric Cancer Care Disparities in Radiotherapy: A Decade Change
ABSTRACT Background We present an update on the status, needs and challenges faced by paediatric imaging and radiotherapy (RT) programmes globally after a previous survey conducted by the International Atomic Energy Agency (IAEA) 10 years prior. Methods We developed and distributed a 121‐question survey to radiation oncologists, medical physicists and ...
Raymond B. Mailhot Vega +10 more
wiley +1 more source
Chemodivergent manganese-catalyzed C–H activation: modular synthesis of fluorogenic probes
Bioorthogonal diversification of peptides is generally dependent on impractical prefunctionalization methods. Here, the authors develop a manganese(I)-catalyzed C–H fluorescent labeling with BODIPY probes, which enables the development of activatable ...
Nikolaos Kaplaneris +7 more
doaj +1 more source
ABSTRACT Background Children with sickle cell anemia (SCA) in low‐income settings are at risk of severe malnutrition, but optimal nutritional management has not been established. We evaluated an intensified ready‐to‐use therapeutic food (RUTF) regimen in children with persistent severe malnutrition after initial treatment and assessed whether early ...
Safiya Gambo +9 more
wiley +1 more source

