Improved Method for the Iodine(III)-Mediated Preparation of Aryl Sulfonimidates
摘要:
One-pot hypervalent iodine-mediated oxidations of arylsulfinamides to arylsulfonimidates is reported. Contrary to the case of alkylsulfinamides, use of iodosobenzene was not satisfactory. The reaction worked best with diacetoxyiodosobenzene (DIB) and a mild base (MgO). The influence of substituents on the iodine(III) reagent arene has been examined.
A Mild and General One-Pot Synthesis of Densely Functionalized Diaryliodonium Salts
作者:Linlin Qin、Bao Hu、Kiel D. Neumann、Ethan J. Linstad、Katelyenn McCauley、Jordan Veness、Jayson J. Kempinger、Stephen G. DiMagno
DOI:10.1002/ejoc.201500986
日期:2015.9
Diaryliodoniumsalts are powerful and widely used arylating agents in organic chemistry. Here we report a scalable, synthesis of densely functionalized diaryliodoniumsaltsfrom aryl iodides under mild conditions. This two-step, one-pot process has remarkable functional group tolerance, is compatible with commonly employed acid-labile protective group strategies, avoids heavy metal and transition metal
二芳基碘鎓盐是有机化学中强大且广泛使用的芳基化剂。在这里,我们报告了在温和条件下从芳基碘化物大规模合成密集官能化二芳基碘鎓盐的方法。这种两步一锅法具有显着的官能团耐受性,与常用的酸不稳定保护基策略兼容,避免重金属和过渡金属试剂,并为 PET 成像剂的稳定前体提供了直接途径。
Blue LED Irradiation of Iodonium Ylides Gives Diradical Intermediates for Efficient Metal‐free Cyclopropanation with Alkenes
作者:Tristan Chidley、Islam Jameel、Shafa Rizwan、Philippe A. Peixoto、Laurent Pouységu、Stéphane Quideau、W. Scott Hopkins、Graham K. Murphy
DOI:10.1002/anie.201908994
日期:2019.11.18
A facile and highly chemoselective synthesis of doubly activated cyclopropanes is reported where mixtures of alkenes and β-dicarbonyl-derived iodoniumylides are irradiated with light from blue LEDs. This metal-free synthesis gives cyclopropanes in yields up to 96 %, is operative with cyclic and acyclic ylides, and proceeds with a variety of electronically-diverse alkenes. Computational analysis explains
(diacetoxyiodo)-arenes, ArI(OAc)2, or iodylarenes, ArIO2, from the corresponding iodoarenes, ArI, using sodium periodate as the oxidant are presented in this paper. In order to obtain 2- and 4-iodylbenzoic acids, the respective sodium salts of 2- and 4-iodobenzoic acids should be used as the starting substrates, because mixtures containing the corresponding iodosyl derivatives as the main products
Synthesis of β-acetoxy alcohols by PhI(OAc)<sub>2</sub>-mediated metal-free diastereoselective β-acetoxylation of alcohols
作者:Chun-Yang Zhao、Liang-Gui Li、Qing-Rong Liu、Cheng-Xue Pan、Gui-Fa Su、Dong-Liang Mo
DOI:10.1039/c6ob01203e
日期:——
β-Acetoxy alcohols can be synthesized in good yields with excellent diastereoselectivity from tertiary alcohols through PhI(OAc)2-mediated metal-free β-acetoxylation. Mechanistic studies showed that the β-acetoxylation process might undergo dehydration and sequential highly regioselective and diastereoseletive dioxygenation. Gram scale and diverse useful scaffolds could be prepared via this β-acetoxylation
Further functional group oxidations using sodium perborate
作者:Alexander McKillop、Duncan Kemp
DOI:10.1016/s0040-4020(01)81008-5
日期:1989.1
Sodiumperborate in acetic acid is an effective reagent for the oxidation of aromatic aldehydes to carboxylic acids, iodoarenes to (diacetoxyiodo)arenes, azines to -oxides, and various types of sulphur heterocycles to ,-dioxides. Nitriles are unaffected by the reagent in acetic acid, but undergo smooth hydration to amides when aqueous methanol is employed as solvent.