Results 11 to 20 of about 22,537 (233)
N-(diisopropylphosphanyl)benzamide
Molbank, 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 +6 more sources
2-(Methylsulfinyl)benzamide [PDF]
Acta Crystallographica Section E Structure Reports Online, 2010 In the crystal of the title compound, C(8)H(9)NO(2)S, synthesized by the oxidation of 2-(methyl-sulfan-yl)benzamide using NaOCl with 2,2,6,6-tetra-methyl-piperidyl-1-oxy (TEMPO) as the catalyst, mol-ecules are linked via inter-molecular N-H⋯O(amide) hydrogen bonds, forming centrosymmetric amide-amide dimers which are extended into a two-dimensional ...
Zhou Yan
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2-Chloro-N-(2,6-dichlorophenyl)benzamide
Acta Crystallographica Section E, 2008 In the structure of the title compound (N26DCP2CBA), C13H8Cl3NO, the conformations of N—H and C=O bonds in the amide group are trans to each other, similar to that observed in N-(2,6-dichlorophenyl)benzamide, 2-chloro-N-phenylbenzamide, 2-chloro-N-(
B. Thimme Gowda +4 more
doaj +2 more sources
Cobalt-Catalyzed Asymmetric Construction of Boron Stereocenters With C-N Axial Chirality. [PDF]
Adv Sci (Weinh)A cobalt/Salox‐catalyzed one‐pot annulation enables enantioselective formation of B‐stereogenic centers and C─N axial chirality via C─H/N─H annulation, affording diverse fluorescent products with high stereocontrol and optoelectronic potential. ABSTRACT The efficient construction of boron stereogenic centers alongside axial chirality remains a ...
Kumaran S +5 more
europepmc +2 more sources
N,N'-1,2-Phenylenebis[4-(chloromethyl)benzamide] [PDF]
Molbank, 2010 N,N'-1,2-Phenylenebis[4-(chloromethyl)benzamide] (3) was obtained in 61% yield by nucleophilic acyl substitution of 4-(chloromethyl)benzoyl chloride (2) with 1,2-phenylenediamine (1) under basic conditions.
Jürgen Bachl, David D. Díaz
doaj +2 more sources
Design, Synthesis, and Evaluation of New 1,4-Naphthoquinone-1,2,3-triazoles as Antimalarial Agents. [PDF]
Chem BiodiversCompound 9g, a 1,4‐naphthoquinone‐1,2,3‐triazole derivative, exhibited potent activity against P. falciparum 3D7 and in silico analysis revealed strong interactions with 1J3 and 1LDG targets, while MD simulations confirmed the stability of the ligand‐3FGO complex.
Rezainia L +13 more
europepmc +2 more sources
Switching Polymorph Stabilities with Impurities: A Thermodynamic Route to Benzamide Form III [PDF]
, 2020 We investigate the polymorphic behavior of benzamide, the first compound known to exhibit polymorphism, in the presence of small amounts of nicotinamide in the crystallization environment. A previous study by Emmerling et al.1 showed that the presence of
Andrea, Carletta +4 more
core +2 more sources
, 2013 (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 ...
K. Shankland (2497582) +5 more
core +5 more sources
, 2009 The 13th International Electronic Conference on Synthetic Organic Chemistry session Symposium on Microwave Assisted SynthesisMicrowave irradiation of N-[2-(phenylmethyl)phenyl]benzamide with potassium tert-butoxide leads to a 1:1 ratio of the expected ...
Seijas Vázquez, Julio Antonio +9 more
core +1 more source
Acta Crystallographica Section E: Crystallographic Communications, 2019 The title compound, C18H18F2N2O3, crystallizes with two independent molecules (A and B) in the asymmetric unit. They differ essentially in the orientation of the pyridine ring with respect to the benzene ring; these two rings are inclined to each other ...
G. Artheswari +2 more
doaj +1 more source