Results 11 to 20 of about 16,265 (239)

Benzamide oxime [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2008
In the crystal structure of the title compound, C(7)H(8)N(2)O, mol-ecules are connected via inter-molecular N-H⋯O and O-H⋯N hydrogen bonds to form a two-dimensional supra-molecular structure. The oxime group has an E configuration and the dihedral angle between the mean planes of the benzene ring and the amidoxime grouping is 20.2 (3)°.
Shu-Qing Xu, Jia-Ming Li
openaire   +3 more sources

N-(diisopropylphosphanyl)benzamide

open access: yesMolbank, 2023
N-(diisopropylphosphanyl)benzamide, PhC(O)NHPiPr2, has been synthesized in good yield following two alternative procedures that employ benzamide as the starting material. The first one is a two-step preparation, in which N-(trimetilsilyl)benzamide is reacted with PiPr2Cl, to give the title compound in good yield, whereas the second one is a ...
María M. Alcaide   +3 more
openaire   +5 more sources

N-(Cyanomethyl)benzamide [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2010
In the structure of the title compound, C(9)H(8)N(2)O, the amide group is twisted by a dihedral angle of 21.86 (7)° with respect to the benzene ring, while the planes of the benzene ring and cyano-methyl group form a dihedral angle of 53.13 (11)°. In the crystal structure, mol-ecules are linked via N-H⋯O hydrogen bonds, forming a chain running parallel
Abdelrhani Elachqar   +4 more
openaire   +3 more sources

Stereoselective Oxidative Cyclization of N-Allyl Benzamides to Oxazolines

open access: yes, 2021
This manuscript describes a highly enantioselective oxidative cyclization of N-Allyl Benzamides and derivatives thereof. This method uses a chiral triazole-based iodine catalyst to generate a hypervalent iodine compound in situ as the active catalytic ...
Ayham, Abazid   +2 more
core   +1 more source

Some imidazolyl benzamides as potent antibacterial agents [PDF]

open access: yes, 2020
A series of imidazolyl benzamides containing urea has been efficiently synthesized and evaluated for their antibacterial properties. Some of the molecules exhibited promising antibacterial activity when compared to the reference standard, Ciprofloxacin. ©
Sajith, A. M.   +11 more
core   +1 more source

Polymorphism in Benzamide

open access: yesAngewandte Chemie, 2005
(Figure Presented) At long last, the crystal structure of the metastable form of benzamide, whose existence has been known of for over 170 years, has finally been solved by using a combination of in situ crystallization, high-speed synchrotron X-ray powder diffraction, and global-optimization methods of structure determination (see picture).
W. I. F. David   +5 more
openaire   +4 more sources

Rh-Catalyzed Oxidative Coupling between Primary and Secondary Benzamides and Alkynes: Synthesis of Polycyclic Amides

open access: yes, 2016
A methodology for the high yield and facile synthesis of isoquinolones from benzamides and alkynes via the oxidative ortho C−H activation of benzamides has been developed.
Dan Chen (32468)   +4 more
core   +4 more sources

Novel Hybrid Formulations Based on Thiourea Derivatives and Core@Shell Fe3O4@C18 Nanostructures for the Development of Antifungal Strategies

open access: yesNanomaterials, 2018
The continuously increasing global impact of fungal infections is requiring the rapid development of novel antifungal agents. Due to their multiple pharmacological activities, thiourea derivatives represent privileged candidates for shaping new drugs. We
Carmen Limban   +8 more
doaj   +1 more source

Enantioselective alpha-Arylation of Benzamides via Synergistic Nickel and Metallaphotoredox Catalysis

open access: yes, 2019
A new method to access alpha-arylated benzamides has been enabled by metallaphotoredox catalysis. This system allows for non-directed C–H functionalization of N-alkyl benzamides using a dual nickel/iridium catalytic system to form tertiary stereocenters ...
John, Montgomery, Alexander W., Rand
core   +2 more sources

N-(4-Chlorophenylsulfonyl)-4-iodobenzamide

open access: yesIUCrData, 2017
In the title compound, C13H9ClINO3S, the benzene rings are inclined to one another by 81.6 (2)°. In the crystal, molecules are linked by pairs of N—H...O hydrogen bonds, forming inversion dimers with an R22(8) ring motif. The dimers are linked by C—H...O
S. Naveen   +5 more
doaj   +1 more source

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