Results 31 to 40 of about 13,855 (240)
5-(4H)-Oxazolones and Their Benzamides as Potential Bioactive Small Molecules
The five membered heterocyclic oxazole group plays an important role in drug discovery. Oxazolones present a wide range of biological activities. In this article the synthesis of 4-substituted-2-phenyloxazol-5(4H)-ones from the appropriate substituted ...
Evangelos Mavridis+3 more
doaj +1 more source
2-(Methylsulfinyl)benzamide [PDF]
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 ...
openaire +4 more sources
Direct conversion of amides to ketones typically requires the use of transition metal catalysts or reactive organometallic reagents. Here the direct alkylation of benzamides with methyl sulfides using LDA as base provides access to thioalkoxyketones.
Can-Can Bao+3 more
doaj +1 more source
Abstract We report the synthesis and X‐ray structures of four Rh2(OAc)4(LAx)2 (OAc=acetate, CH3COO−) paddle‐wheel complexes (C1−C4) with methylthio‐modified axial ligands LAx derived from benzamidine (L1), anilinopyrimidine (L2) or isothiourea (L3, L4) that are capable of forming N−H⋅⋅⋅O hydrogen bonds to the equatorially bridging acetate ligands. This
André Mang+2 more
wiley +1 more source
Click‐chemistry compatible azobenzenes are synthesized and coupled on various positions at the surface of a disulfide‐bridged natural peptide. Monomers and dimers are produced and linked by azobenzene. The impact of azobenzene photoswitching on the ion channel blocking potency of the peptide is evaluated and revealed that proper positioning leads to ...
Yanis Achouba+18 more
wiley +2 more sources
Three newly synthesized benzamides by the Department of Pharmaceutical Chemistry of the Faculty of pharmacy from the University of Medicine and Pharmacy „Carol Davila” Bucharest were tested in order to determine whether these new molecules have similar ...
Cornel Chiriță+4 more
doaj +1 more source
The discovery of LIBX‐A401, a potent and selective ACSL4 inhibitor derived from rosiglitazone is reported. HDX‐MS reveals that LIBX‐A401 stabilizes the ACSL4 C‐terminus and alters the fatty acid (FA) gate domain. Consistently, photoaffinity labeling, molecular dynamics, and mutagenesis identify key binding residues within the FA pocket.
Darius Mazhari Dorooee+19 more
wiley +2 more sources
4-Iodo-N-(phenylsulfonyl)benzamide hemihydrate
In the title hemihydrate, 2C13H10INO3S·H2O, there are two organic molecules (A and B) and one water molecule in the asymmetric unit. The benzene rings are inclined to one another by 77.98 (1)° in A and 79.81 (9)° in B. The A and B molecules are connected
P. A. Suchetan+5 more
doaj +1 more source
N-(2,6-Dichlorophenyl)benzamide [PDF]
The conformation of the N-H and C=O bonds in the structure of the title compound (N26DCPBA), C(13)H(9)Cl(2)NO, are anti to each other, similar to that observed in N-phenyl-benzamide (NPBA), N-(2-chloro-phen-yl)benzamide (N2CPBA), N-(2,3-dichloro-phen-yl)benzamide (N23DCPBA) and other benzanilides. The asymmetric unit of N26DCPBA contains two mol-ecules.
Hartmut Fuess+4 more
openaire +4 more sources
Benzamide‐directed iridium‐catalyzed branched selective and enantioselective C(sp2)‐H additions to minimally activated alkenes give tertiary and quaternary benzylic stereocenters under byproduct‐free conditions. The processes are enabled by a family of SPINOL‐based homochiral diphosphonite ligands.
Timothy P. Aldhous+9 more
wiley +2 more sources