Advancing the logic of chemical synthesis: C− H activation as strategic and tactical disconnections for C− C bond construction
The design of synthetic routes by retrosynthetic logic is decisively influenced by the
transformations available. Transition‐metal‐catalyzed C− H activation has emerged as a …
transformations available. Transition‐metal‐catalyzed C− H activation has emerged as a …
Oxidative C–H/C–H coupling reactions between two (hetero) arenes
Y Yang, J Lan, J You - Chemical reviews, 2017 - ACS Publications
Transition metal-mediated C–H bond activation and functionalization represent one of the
most straightforward and powerful tools in modern organic synthetic chemistry. Bi (hetero) …
most straightforward and powerful tools in modern organic synthetic chemistry. Bi (hetero) …
C–H functionalization of azines
Azines, which are six-membered aromatic compounds containing one or more nitrogen
atoms, serve as ubiquitous structural cores of aromatic species with important applications in …
atoms, serve as ubiquitous structural cores of aromatic species with important applications in …
Oxidative coupling between two hydrocarbons: an update of recent C–H functionalizations
C− C bond formation is a fundamental transformation in organic synthesis. The development
of new synthetic methodology could be considered as a way of pursuing a novel method for …
of new synthetic methodology could be considered as a way of pursuing a novel method for …
Cross‐Coupling of Heteroarenes by C H Functionalization: Recent Progress towards Direct Arylation and Heteroarylation Reactions Involving Heteroarenes …
In recent years, transition metal‐catalyzed direct (hetero) arylation reactions of heteroarenes
with (hetero) aryl halides and pseudohalides have received significant attention as eco …
with (hetero) aryl halides and pseudohalides have received significant attention as eco …
Rhodium-catalyzed C–H activation of phenacyl ammonium salts assisted by an oxidizing C–N bond: a combination of experimental and theoretical studies
Rh (III)-catalyzed C–H activation assisted by an oxidizing directing group has evolved to a
mild and redox-economic strategy for the construction of heterocycles. Despite the success …
mild and redox-economic strategy for the construction of heterocycles. Despite the success …
Regioselective Introduction of Heteroatoms at the C-8 Position of Quinoline N-Oxides: Remote C–H Activation Using N-Oxide as a Step** Stone
Reported herein is the metal-catalyzed regioselective C–H functionalization of quinoline N-
oxides at the 8-position: direct iodination and amidation were developed using rhodium and …
oxides at the 8-position: direct iodination and amidation were developed using rhodium and …
Transition-metal-catalyzed site-selective C–H functionalization of quinolines beyond C2 selectivity
T Iwai, M Sawamura - ACS Catalysis, 2015 - ACS Publications
Quinoline is an important scaffold in many natural products, biologically active compounds,
and functional materials. The C–H functionalization of quinoline scaffolds by transition metal …
and functional materials. The C–H functionalization of quinoline scaffolds by transition metal …
Recent advances in the synthesis and reactivity of quinoxaline
Quinoxaline has become a subject of extensive research due to its emergence as an
important chemical moiety, demonstrating a wide range of physicochemical and biological …
important chemical moiety, demonstrating a wide range of physicochemical and biological …
Mechanism of the palladium-catalyzed arene C–H acetoxylation: A comparison of catalysts and ligand effects
AK Cook, MS Sanford - Journal of the American Chemical Society, 2015 - ACS Publications
This article describes detailed mechanistic studies focused on elucidating the impact of
pyridine ligands on the Pd-catalyzed C–H acetoxylation of benzene. Three different …
pyridine ligands on the Pd-catalyzed C–H acetoxylation of benzene. Three different …