79347-82-3Relevant academic research and scientific papers
Three-Component Ring-Opening Reactions of Cyclic Ethers, α-Diazo Esters, and Weak Nucleophiles under Metal-Free Conditions
Lu, Lin,Chen, Chuwei,Jiang, Huanfeng,Yin, Biaolin
, p. 14385 - 14395 (2018)
A protocol for three-component reactions of cyclic ethers, α-diazo esters, and weak nitrogen, oxygen, carbon, and sulfur nucleophiles (pKa = 2.2-14.8) to afford a variety of structurally complex α-oxyalkylated esters is reported. These reactions involve intermolecular activation of the cyclic ether (present in excess) by the α-diazo ester to form an oxonium ylide under metal-free conditions, followed by ring opening by the nucleophile.
Synthesis and structure of the dimeric copper(II) complex tetrakis[N-thiazol-2-yl-(4-methylphenyl)sulfonamidate]dicopper(II)
Cabaleiro, Santiago,Calvo, Rafael,Castro, Jesus,Garcia-Vazquez, J. Arturo,Napolitano, Lia M. B.,Nascimento, Otaciro R.,Perez-Lourido, Paulo,Romero, Jaime,Sousa, Antonio
, p. 71 - 75 (2008)
The coordination chemistry of the ligand N-thiazol-2-yl- toluenesulfonamidate towards the copper(II) ion has been investigated using an electrochemical synthesis method. The X-ray structure of this complex was elucidated and is discussed. The compound cry
METHOD FOR REMOVING DIMETHOXYBENZYL GROUP
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Paragraph 0341; 0347; 0348; 0349, (2018/09/23)
In a method for producing a de-dimethoxybenzylated compound by removing a dimethoxybenzyl group from a compound containing a dimethoxybenzyl group bonded to a nitrogen atom in the presence of an acid, the de-dimethoxybenzylated compound is obtained by rem
Molecular modeling, synthesis, antibacterial and cytotoxicity evaluation of sulfonamide derivatives of benzimidazole, indazole, benzothiazole and thiazole
Naaz, Farha,Srivastava, Ritika,Singh, Anuradha,Singh, Nidhi,Verma, Rajesh,Singh, Vishal K.,Singh, Ramendra K.
, p. 3414 - 3428 (2018/05/23)
A new series of heterocyclic molecules bearing sulfonamide linkage has been synthesized and screened for antibacterial activity. During antibacterial screening using broath dilution method, molecules were found to be highly active (MIC value 50–3.1 μg/mL)
