Stepwise Mechanism for the Bromination of Arenes by a Hypervalent Iodine Reagent
作者:Albert Granados、Alexandr Shafir、Ana Arrieta、Fernando P. Cossío、Adelina Vallribera
DOI:10.1021/acs.joc.9b02784
日期:2020.2.21
A mild, metal-free bromination method of arenes has been developed using the combination of bis(trifluoroacetoxy)iodobencene and trimethylsilyl bromide. In situ-formed dibromo(phenyl)-λ3-iodane (PhIBr2) is proposed as the reactive intermediate. This methodology using PIFA/TMSBr has been applied with success to a great number of substrates (25 examples). The treatment of mono-substituted activated arenes
An object of the present invention is to provide a novel substance that has a high reactivity as a fluorinating agent, is effectively used in various fluorination reactions, and is safely handled even in air. As the solution for achieving this object, the present invention provides a complex obtained by reacting bromine trifluoride with at least one metal halide selected from the group consisting of halogenated metals and halogenated hydrogen metals in a nonpolar solvent. This complex serves as a fluorinating agent that provides excellent fluorination performance and that is stable in air.
Synthesis and Application of a New Class of Planar and Centrally Chiral Ferrocenyl Amino Alcohol Ligands
作者:Annette Benson、Laura Cunningham、Patrick J. Guiry
DOI:10.1002/ejoc.202300951
日期:——
The highly enantioselective, facile, scalable, and robust synthesis of a new family (14 examples) of aminoalcohol ligands possessing planar and central chirality that is described. They were applied to the diethylzinc and diphenylzinc additions to aldehydes with up to 98 % yield and 99 % ee and 82 % yield and 88 % ee, respectively.
BrF3-KHF2, an air-stable solid prepared from BrF3 and KHF2, was used in the various fluorination reactions, including desulfurizing fluorination reactions of benzylic sulfides, ketone and aldehyde dithioacetals, (phenylthio)glycosides, and trimethyl trithioorthocarboxylates. As the results, one to three fluorine atoms were selectively introduced to the substrates. (C) 2014 Elsevier B.V. All rights reserved.
Palladium/Copper-Catalyzed Oxidative CH Alkenylation/N-Dealkylative Carbonylation of Tertiary Anilines
作者:Renyi Shi、Lijun Lu、Hua Zhang、Borui Chen、Yuchen Sha、Chao Liu、Aiwen Lei
DOI:10.1002/anie.201303911
日期:2013.9.27
CH/CN activation: The first palladium/copper‐catalyzed aerobic oxidative CH alkenylation/N‐dealkylative carbonylation of tertiary anilines has been developed. Various functional groups were tolerated and acrylic ester could also be suitable substrates. This transformation provided efficient and straightforward synthesis of biologically active 3‐methyleneindolin‐2‐one derivatives from cheap and simple
Ç H / C Ñ活化:第一钯/铜催化氧化好氧Ç ħ烯基/ Ñ叔苯胺-dealkylative羰基化得到了发展。可以容忍各种官能团,丙烯酸酯也可以用作合适的底物。这种转化提供了从廉价,简单的底物中高效,直接地合成具有生物活性的3-亚甲基吲哚-2-酮衍生物的功能。