A novel visible-light-photocatalytic deuterated thiomethylation/methylselenation of aryldiazonium salts utilizing /methyl- sulfonothioate has been developed. The mild conditions and the various functional groups provide a green protocol for the efficient and rapid introduction of the -CD or -CD group with useful levels of deuterium content (>91% D). Trideuteromethyl sulfoxides have also been successfully chemoselectively observed by simple atmospheric changes under photocatalytic conditions.
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http://dx.doi.org/10.1021/acs.orglett.0c03562 | DOI Listing |
J Org Chem
October 2024
Department of Chemistry, Chonnam National University, Gwangju 61186, Republic of Korea.
We developed a method for synthesizing aryl alkyl thioether compounds via a three-component reaction involving aryldiazonium salts, 1,4-diazabicyclo[2.2.2]octane bis(sulfur dioxide), and alkyl bromides.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2024
Department of Chemistry, University of Southern California, California, Los Angeles 90089, United States.
The storage of renewable energy through the conversion of CO to CO provides a viable solution for the intermittent nature of these energy sources. The immobilization of rhenium(I) tricarbonyl molecular complexes is presented through the reductive coupling of bis(diazonium) aryl substituents. The heterogenized complex was characterized through ultra-visible, attenuated total reflectance, infrared reflection absorption spectroscopy, and X-ray photoelectron spectroscopy to probe the electronic structure of the immobilized complex.
View Article and Find Full Text PDFTurk J Chem
March 2024
Department of Chemistry, Faculty of Science, Atatürk University, Erzurum, Turkiye.
A practical, rapid, and efficient method for the synthesis of azoindolizine derivatives via aryldiazonium salts with excellent yields was reported. Firstly, the corresponding aniline derivatives were synthesized via a simple and rapid method. Then, the optimal reaction conditions were investigated using a variety of protic and aprotic solvents that demonstrating the robustness of the approach.
View Article and Find Full Text PDFJ Org Chem
July 2024
Instituto de Química, Universidad Nacional Autónoma de México, Circuito Exterior s/n, Ciudad Universitaria, Ciudad de México 04510, México.
We describe herein a gold-catalyzed three-component reaction of -alkynylbenzaldehydes, aryldiazonium salts, and trimethoxybenzene. This process enables the one-pot formation of valuable isoindoles and 1,2-dihydrophathalazines. The regioselectivity of the reaction is dictated by the nature of the aryldiazonium salt.
View Article and Find Full Text PDFOrg Lett
June 2024
Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming 650500, China.
An unprecedented selective chromone annulation reaction controlled by solvent for the divergent synthesis of two types of 2,3-disubstituted chromone skeletons has been developed. A variety of 2-chromonyl-3-hydrazono-chromones and 2-alkoxy-3-hydrazono-chromones were constructed efficiently from readily available -hydroxyphenylenaminones (-HPEs) and aryldiazonium salts at room temperature. This strategy is highly chemoselective and features mild reaction conditions, broad substrate scope, broad functional group tolerance, easy gram-scale preparation, and simple filtration to obtain the pure products without tedious column chromatography.
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