Ligand free, highly efficient synthesis of diaryl ether over copper fluorapatite as heterogeneous reusable catalyst
作者:Shafeek A.R. Mulla、Suleman M. Inamdar、Mohsinkhan Y. Pathan、Santosh S. Chavan
DOI:10.1016/j.tetlet.2012.01.124
日期:2012.4
A novel ligand-free, highlyefficient, and an inexpensive method has been developed by using ecofriendly, heterogeneous reusable copper fluorapatite (CuFAP) catalyst for the synthesis of diaryl ethers from the cross coupling reaction of the various substituted aryl halides (fluoride, chloride, bromide, and iodide) with the potassium salts of various substituted phenols in the presence of N-methyl 2-pyrrolidone
A facile and rapid method for the synthesis of novel imidazole and benzimidazole aromatic acyclic nucleosides is described. Synchronous N-alkylation of imidazole or benzimidazole and potassium aryloxide with methylene iodide in the presence of triethylamine and a catalytic amount of tetrabutylammonium bromide (TBAB) in dry acetonitrile or acetone gave moderate yields of the acycloaromatic nucleoside
Synthesis of 6<i>H-</i>Benzo[<i>c</i>]chromene Scaffolds from <i>O</i>-Benzylated Phenols through a C–H Sulfenylation/Radical Cyclization Sequence
作者:Steve Karreman、Simon B. H. Karnbrock、Sebastian Kolle、Christopher Golz、Manuel Alcarazo
DOI:10.1021/acs.orglett.1c00087
日期:2021.3.19
S-Aryl dibenzothiophenium salts, obtained through a highly regioselective C–H sulfenylation of o-benzyl-protected phenols, are used as precursors of 6H-benzo[c]chromenes. The reaction starts with a photocatalytically triggered single-electron transfer to the sulfonium salt, which promotes the formation of an arylradical via selective mesolitic cleavage of the S–Arexo bond. Mechanistic studies reveal
S-芳基二苯并噻吩鎓盐是通过邻苯甲基保护的苯酚的高区域选择性 C-H 亚磺酰化获得的,用作 6 H-苯并[ c ]色烯的前体。该反应从光催化触发的单电子转移到锍盐开始,这通过选择性中间体裂解 S-Ar外键促进芳基自由基的形成。机理研究表明,这种最初的自由基物种遵循动力学有利的 5-exo-trig 途径循环。随后的环扩展,有利于重芳构化,提供所需的三环系统。
Substituted 2-phenyl-3(2h)-pyridazinones
申请人:Schohe-Loop Rudolf
公开号:US20060004015A1
公开(公告)日:2006-01-05
The invention relates to substituted 2-phenyl-3(2h)-pyridazinones, to a method for the production thereof, and to their use as medicaments used in the prophylaxis and/or treatment of diseases in humans and/or animals.
Synthesis method for a compound used to form a self-assembled monolayer, compound for forming a self-assembled monolayer, and layer structure for a semiconductor component
申请人:Effenberger Franz
公开号:US20060160272A1
公开(公告)日:2006-07-20
A synthesis method of a compound used to form a self-assembled monolayer used in a semiconductor component is provided. A method includes a first step of replacing a terminal halogen of an ω-haloalk-1-ene with a compound having at least one aromatic group, and a second step of hydrosilylating the reaction product of the first step. Reaction products of the first step include octadec-17-enyloxybenzene, 4-octadec-17″-enyloxy-1,1′-biphenyl, 2-heptadec-16′-enylthiophene, and 2-octadec-17′-enylthiophene. Monolayers provided include 18-phenoxyoctadecyl)trichlorosilane, [18-(1′,1″-biphenyl-4′-yloxy)octadecyl]trichlorosilane, (17-thien-2′-ylheptadecyl)trichlorosilane, (18-thien-2′-yloctadecyl)trichlorosilane, and 4-(18′-trichlorosilyloctadecyloxy)benzonitrile. An organic field effect transistor having monolayers according to embodiments of the invention is provided.