Results 41 to 50 of about 22,537 (233)
Isoxazole derivatives (isoxazoles, isoxazolines, and isoxazolidines) are present in the structure of several natural products and/or pharmaceutically interesting compounds.
Konstantinos A. Ouzounthanasis +3 more
doaj +1 more source
Crystal structure of 4-chloro-N-[2-(piperidin-1-yl)ethyl]benzamide monohydrate
In the title compound, C14H19ClN2O2·H2O, the piperdine ring adopts a chair conformation. The dihedral angle between the mean plane of the piperidine ring and that of the phenyl ring is 41.64 (1)°.
K. Prathebha +4 more
doaj +1 more source
Allenes emerge as powerful platforms for electrochemical functionalization through radical pathways. Selective radical addition at the central carbon triggers anodic oxidation and intramolecular cyclization, enabling efficient synthesis of oxazolines and oxazolidine‐2‐imines without external oxidants.
Pranjal Pyne +5 more
wiley +1 more source
Analysis of a Benzamide/Cholesterol Mixture by Using TLC/FTIR Technique [PDF]
We applied TLC/FTIR coupled with a mapping technique to analyze a cholesterol/benzamide mixture. Narrow-band TLC plates by using AgI as a stationary phase were used to separate benzamide and cholesterol.
Wu, Jinguang +23 more
core +1 more source
Crystal structure of 4-methoxy-N-[(pyrrolidin-1-yl)carbothioyl]benzamide
In the title compound, C13H16N2O2S, the pyrrolidine ring has a twisted conformation on the central –CH2–CH2– bond. Its mean plane is inclined to the 4-methoxybenzoyl ring by 72.79 (15)°.
Khairi Suhud +4 more
doaj +1 more source
A nickel‐catalyzed three‐component reductive fluoroalkylation‐amination strategy of N‐vinylamides for the direct access to the α‐amidyl‐β‐difluoroalkyl amines was reported here. The synthetic method features with broad substrate scope, mild conditions, high functional group tolerance, and convenience to handle.
Chang Xu +8 more
wiley +1 more source
N-(2,6-Dichlorophenyl)benzamide
The conformation of the N—H and C=O bonds in the structure of the title compound (N26DCPBA), C13H9Cl2NO, are anti to each other, similar to that observed in N-phenylbenzamide (NPBA), N-(2-chlorophenyl)benzamide (N2CPBA), N-(2,3-dichlorophenyl ...
B. P. Sowmya +4 more
core +1 more source
N,N′-(Ethane-1,2-diyl)bis(2-chlorobenzamide)
The title compound, C16H14Cl2N2O2, crystallized with one half-molecule in the asymmetric unit; the whole molecule is generated by inversion symmetry, the center of inversion being situated at the middle of the bridging –CH2—CH2– bond.
U. Mohamooda Sumaya +4 more
doaj +1 more source
NiH‐Catalyzed Enantio‐ and Regioselective Hydroselenylation of Unactivated Alkenes
Nickel‐hydride‐catalyzed enantio‐ and regioselective hydroselenylation of unactivated alkenes provides access to chiral organoselenium compounds. Enantiodetermining Ni–H insertion followed by single‐electron diselenide activation generates selenyl radical.
Hyung‐Joon Kang +2 more
wiley +1 more source
Aggregation in Three Benzamide or Pyridylcarboxamide Hydrates: Formation of 1D Chains Comprising Water Molecules in a Chloro(pyridyl)benzamide Dihydrate [PDF]
Three benzamide hydrated derivatives as para-methyl-N-(3-pyridyl)benzamide monohydrate (I) or Mpm ∙ H2O; N-(3-fluorophenyl)-4-pyridylcarboxamide monohydrate (II) or NpmF ∙ H2O and para-chloro-N-(3-pyridyl)benzamide dihydrate (III) or Clpm ∙ 2H2O are ...
Gallagher, John F. +6 more
core +1 more source

