Results 11 to 20 of about 679,684 (301)
Palladium-Catalyzed Decarboxylative ortho-Acylation of Anilines with Carbamate as a Removable Directing Group [PDF]
Qi-Li Li, Zhong-Yuan Li, Guan-Wu Wang
doaj +2 more sources
Copper-mediated oxidative C−H/N−H activations with alkynes by removable hydrazides
The efficient copper-mediated oxidative C–H alkynylation of benzhydrazides was accomplished with terminal alkynes. Thus, a heteroaromatic removable N-2-pyridylhydrazide allowed for domino C–H/N–H functionalization.
Feng Xiong +7 more
doaj +1 more source
Synthesis of Polysubstituted Ferrocenesulfoxides
The purpose of the study is to design synthetic methodologies, especially directed deprotometalation using polar organometallic reagents, to access polysubstituted ferrocenesulfoxides.
Min Wen +6 more
doaj +1 more source
Imine as a linchpin approach for meta-C–H functionalization
Site-selective C–H functionalization still faces some challenges, such as the introduction and removal of an appropriate directing group. Here, the authors introduce a temporary directing group for selective meta-C–H functionalization of 2 ...
Sukdev Bag +6 more
doaj +1 more source
Set-direct factorizations of groups [PDF]
referee comments included, 19 ...
Levy, Dan, Maróti, Attila
openaire +2 more sources
Distal Functionalization via Transition Metal Catalysis
The ubiquitous presence of sp3 C−H bonds in natural feedstock makes them inexpensive, easily accessible, and attractive synthons for the preparation of common and/or complex molecular frameworks in biologically active natural products, pharmaceutics ...
Haibo Ge
doaj +1 more source
Transition-metal-catalyzed C–H bond functionalization has attracted tremendous attention as an increasingly important protocol for the construction of C–C and C–X bonds.
Jian Zhang +5 more
doaj +1 more source
First selective direct mono-arylation of piperidines using ruthenium-catalyzed C–H activation [PDF]
: A Ru-catalyzed mono-arylation in α-position of saturated cyclic amines is reported employing a C–H activation protocol. Substitution of the pyridine directing group with a bulky group, e.g., trifluoromethyl in the 3-position, proved to be crucial to ...
Karl Kirchner +4 more
core +1 more source
Functional group directed C–H borylation [PDF]
Different strategies designed to enable directing group effects have been applied to achieve regioselective borylation of C(sp2)–H and C(sp3)–H bonds.
Ros Lao, Abel +2 more
openaire +5 more sources
Selective C(sp2)−H Halogenation of "click" 4-Aryl-1,2,3-triazoles [PDF]
Selective bromination reactions of “click compounds” are described. Electron-neutral and electron-deficient arenes selectively undergo unprecedented Pd-catalyzed C–H ortho-halogenations assisted by simple triazoles as modular directing groups, whereas ...
Correa Navarro, Arkaitz +2 more
core +2 more sources

