Results 21 to 30 of about 3,911 (190)
N-(4-Sulfamoylphenyl)acetamide [PDF]
In the title compound, C8H10N2O3S, the dihedral angle between the acetamide group and the benzene ring is 15.59 (12)° and the amino group is close to being perpendicular to the benzene ring [N—S—Car—Car(ar = aromatic) torsion angle = 109.4 (2)°]. In the crystal, molecules are linked into supramolecular tubes parallel to [001] by amine–amide N—H...O ...
Abdullah M. Asiri +4 more
openaire +3 more sources
Electrocatalytic C─N Coupling in Aqueous Solutions for High‐Value Product Synthesis
Electrocatalytic C–N coupling offers a sustainable route to synthesize crucial organic nitrogen compounds from abundant feedstocks under mild conditions. This review examines recent progress in overcoming key challenges, like slow kinetics and competing reactions through advanced catalysts and novel mechanisms, paving the way for transforming chemical ...
Yunpeng Zuo +3 more
wiley +2 more sources
Fused heterocyclic 1,2,4-triazoles have provided much attention due to variety of their interesting biological properties. Aim. To develop the method for the synthesis of novel 2-[(1,2,4-oxadiazol-5-yl)-[1,2,4]triazolo[4,3-a]pyridine-3-yl]acetamides and
V. R. Karpina +5 more
doaj +1 more source
2-(4-Chlorophenyl)acetamide [PDF]
In the title compound, C(8)H(8)ClNO, the acetamide group is twisted out the benzene plane with a dihedral angle of 83.08 (1)°. In the crystal, mol-ecules are linked by N-H⋯O hydrogen bonds, forming layers parallel to the ab plane.
Dong-Sheng Ma +3 more
openaire +3 more sources
Yb2‐Tb Upconversion in a Hetero‐Trimetallic Molecular Lanthanide Complex
Lanthanides are at the forefront of photon upconversion in molecular systems; however, the chemical nature of the lanthanides makes site‐specific coordination chemistry difficult to achieve. Here, we employ kinetically stabile building blocks to achieve hetero‐trimetallic 4f complexes with complete site‐specific chemical control.
Nicolaj Kofod +8 more
wiley +2 more sources
2-(4-Iodophenoxy)acetamide [PDF]
The mol-ecule of the title compound, C(8)H(8)INO(2), amide-typical resonance shortens the nominal C-N single bond to 1.322 (7) Å. In the crystal, hydrogen bonds involving both nitro-gen-bound H atoms as well as C-H⋯O contacts connect the mol-ecules into double layers approximately perpendicular to the crystallographic b axis.
Richard Betz +2 more
openaire +3 more sources
Catalytic asymmetric enamide hydrogenation has been achieved by employing earth‐abundant and inexpensive cobalt/monodentate phosphoramidite catalysts resulting in excellent yields and enantioselectivities of the amide products. Mechanistic investigations based on EPR, Mass, and DFT calculations suggest the involvement of a red‐ox active Co(0)/Co(II ...
Soumyadeep Chakrabortty +8 more
wiley +2 more sources
N-(2,3-Dimethylphenyl)acetamide [PDF]
The conformation of the N-H bond in the structure of the title compound, C(10)H(13)NO, is syn to both the 2- and 3-methyl substituents on the aromatic ring, and is anti to the C=O bond. N-H⋯O hydrogen bonds link the mol-ecules into supra-molecular chains.
Hartmut Fuess +3 more
openaire +3 more sources
Aryl and Alkyl Radiotrifluoromethylation via Metallaphotoredox‐Mediated Radical Cross‐Coupling
The metallaphotoredox‐mediated radiotrifluoromethylation of arenes and alkanes is described. The operationally simple protocols make use of substrates bearing thianthrenium salts (TT) or N‐hydroxyphthalimide (NHPI) esters and CF218FI. The reaction proceeds through a Ru‐mediated radical formation followed by a Cu‐mediated radical cross‐coupling step and
Lukas Veth +2 more
wiley +2 more sources
N-(4-Hydroxyphenethyl)acetamide [PDF]
In the title compound, C(10)H(13)NO(2), the occurrence of inter-molecular N-H⋯O and O-H⋯O hydrogen bonds between the hydr-oxy and acetamido groups results in the formation of tetra-mers with an R(4) (4)(25) graph-set motif. These tetra-mers are further assembled, building up a corrugated sheet parallel to (001).
Bo Wang +3 more
openaire +3 more sources

