Results 131 to 140 of about 12,040 (158)
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Organic Letters, 2019
A fast and simple method for deoxyfluorination of carboxylic acids is presented. The protocol employs commodity chemicals (PPh3, NBS, fluoride), affording products in excellent yields under mild conditions. Acyloxyphosphonium ion, the key reaction intermediate, was identified by NMR spectroscopic methods.
Socrates B. Munoz +4 more
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A fast and simple method for deoxyfluorination of carboxylic acids is presented. The protocol employs commodity chemicals (PPh3, NBS, fluoride), affording products in excellent yields under mild conditions. Acyloxyphosphonium ion, the key reaction intermediate, was identified by NMR spectroscopic methods.
Socrates B. Munoz +4 more
openaire +2 more sources
Organic Letters
We report herein a photoinduced nickel-catalyzed 1,2-acylcyanation of styrenes with acyl fluorides and trimethylsilyl cyanide (TMSCN). Nickel(II) acyl complexes, formed from nickel(0) complexes and acyl fluorides, are photoexcited to generate acyl radicals via a ligand-to-metal charge transfer (LMCT) process.
Naoki Oku +4 more
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We report herein a photoinduced nickel-catalyzed 1,2-acylcyanation of styrenes with acyl fluorides and trimethylsilyl cyanide (TMSCN). Nickel(II) acyl complexes, formed from nickel(0) complexes and acyl fluorides, are photoexcited to generate acyl radicals via a ligand-to-metal charge transfer (LMCT) process.
Naoki Oku +4 more
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Recent Advances in Transformation of Acyl Fluorides
Journal of Synthetic Organic Chemistry, Japan, 2020Yuka Sakurai, Yohei Ogiwara, Norio Sakai
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Phosphine‐Catalyzed Acyl‐Group Exchange Reaction of Carboxylic Acids and an Aroyl Fluoride
European Journal of Organic Chemistry, 2022Kento Ishida +2 more
exaly
Inter- and Intramolecular Acylations with Hydrogen Fluoride
Journal of the American Chemical Society, 1939Louis F. Fieser, E. B. Hershberg
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Acyl Fluorides as Substrates in N-Hetereocyclic (NHC) Catalysis via Unsaturated Acyl Azoliums
2019This thesis describes the discovery and exploration of novel chemical reactions exploiting N-heterocyclic carbenes as organocatalysts.
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