Reductive alkynylation of aldehydes by the Umpolung approach was developed using a photoredox catalyst under blue LED irradiation. Ketyl radicals, generated by single-electron reduction of aldehydes through proton-coupled electron transfer (PCET), reacted with electrophilic alkynylsulfones. Sterically demanding bulky aldehydes reacted smoothly under the Umpolung reaction conditions. Moreover, the alkynylation proceeded chemoselectively with an aryl aldehyde group in the presence of other carbonyl groups including an aliphatic aldehyde group.
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http://dx.doi.org/10.1021/acs.orglett.1c03927 | DOI Listing |
RSC Adv
November 2024
The Affiliated Ganzhou Hospital, Jiangxi Medical College, Nanchang University Ganzhou 341000 Jiangxi Province P. R. China
Sulfonamides are valuable structural building blocks, bioactives, and pharmaceuticals. While there have been great achievements in the sulfonamidation of alkyl and alkenyl carbon, the sulfonamidation of alkynyl carbon has not been studied. Herein, we report the synthesis of -benzylated sulfonamides from alkoxy aryl alkynes and sulfonamides enabled by Ir-catalyzed reductive sulfonamidation using HCOH as a hydrogen donor.
View Article and Find Full Text PDFJ Phys Chem Lett
November 2024
Department of Chemistry, Graduate School of Science, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.
Previous studies have reported that [PdAu(PA)] (PA = 3,5-(CF)CHC≡C) with an icosahedral superatomic PdAu(8e) core underwent collision-induced sequential reductive elimination (CISRE) of 1,3-diyne (PA) ( 2020, 124, 19119). The most likely scenario after the CISRE of (PA) is the growth of the PdAu(8e) core via the fusion of the Au(0) atoms produced from the Au(PA) units on the core surface. Contrary to expectation, anion photoelectron spectroscopy and theoretical calculations regarding the CISRE products [PdAu(PA)] ( = 1-6) revealed that the electronically closed PdAu(8e) core does not grow to a single superatom with (8 + 2)e but assembles with Au(2e) units.
View Article and Find Full Text PDFInt J Mol Sci
September 2024
Natural Compounds and Organic Synthesis Laboratory, Migal-Galilee Research Institute, Kiryat Shmona 11016, Israel.
Chiral pincer complexes, characterized by their rigid tridentate coordination framework, have emerged as powerful catalysts in asymmetric synthesis. This review provides a comprehensive overview of recent advancements in the development of chiral pincer-type ligands and their corresponding transition metal complexes. We highlight the latest progress in their application across a range of catalytic asymmetric reactions, including the (transfer) hydrogenation of polar and non-polar bonds, hydrophosphination, alkynylation, Friedel-Crafts reactions, enantioselective reductive cyclization of alkynyl-tethered cyclohexadienones, enantioselective hydrosilylation, as well as Aza-Morita-Baylis-Hillman reactions.
View Article and Find Full Text PDFPhytomedicine
November 2024
State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy and Tianjin Key Laboratory of Molecular Drug Research, Nankai University, Tianjin, PR China. Electronic address:
Background: Fever is one of the main pathophysiological reactions that occurs during the acute phase of various diseases. Excessive body temperature can lead to various adverse consequences such as brain tissue damage and abnormal immune responses. Phillyrin (Phr) is the main active ingredient in Forsythia suspensa (Thunb.
View Article and Find Full Text PDFOrg Lett
September 2024
State Key Laboratory of Coordination Chemistry, MOE Key Laboratory of High Performance Polymer Materials and Technology, Jiangsu Key Laboratory of Advanced Organic Materials, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210023, China.
α-Amino-CF compounds are widely employed in bio- and pharmaceutical chemistry for improved stability and bioactivities. Traditional methods often face challenges with functional group tolerance and lack a general approach for late-stage functionalization. Herein, we report a new type of redox-active α-amino-CF reagents, easily prepared from trifluoro acetaldehyde hydrates.
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