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pro vyhledávání: '"Ferrocenium hexafluorophosphate"'
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Akademický článek
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Autor:
Fedor M. Dolgushin, A. Z. Kreindlin, Aleksandr A. Chamkin, Vasily V. Krivykh, Nikolai A. Ustynyuk
Publikováno v:
European Journal of Inorganic Chemistry. 2021:1601-1610
Publikováno v:
ACS Sustainable Chemistry & Engineering. 7:479-486
A ferrocenium promoted method for the chemoselective oxidation of benzylic amines to imines has been developed with yields varying from 53% to 93%. Use of 5 mol % ferrocenium hexafluorophosphate as...
Publikováno v:
Free Radical Research. 50:S6-S17
A novel approach to the diazabicyclo[2.2.2]octane core of prenylated bridged diketopiperazine alkaloids is described by direct oxidative cyclizations of functionalized diketopiperazines mediated by ferrocenium hexafluorophosphate or the Mn(OAc)3•2H
Publikováno v:
Biochimica et Biophysica Acta. Proteins and Proteomics
Biochimica et Biophysica Acta (BBA)-Proteins and Proteomics
Biochimica et Biophysica Acta (BBA)-Proteins and Proteomics
Pyranose oxidase (POx) catalyzes the oxidation of d-glucose to 2-ketoglucose with concurrent reduction of oxygen to H2O2. POx from Trametes ochracea (ToPOx) is known to react with alternative electron acceptors including 1,4-benzoquinone (1,4-BQ), 2,
Autor:
Kevin B. Vincent, Jean René Hamon, Rim Makhoul, Jean François Halet, Claude Lapinte, Paul J. Low, Josef B. G. Gluyas, Hiba Sahnoune
Publikováno v:
Organometallics
Organometallics, American Chemical Society, 2018, 37 (21), pp.4156-4171. ⟨10.1021/acs.organomet.8b00740⟩
Organometallics, 2018, 37 (21), pp.4156-4171. ⟨10.1021/acs.organomet.8b00740⟩
Organometallics, American Chemical Society, 2018, 37 (21), pp.4156-4171. ⟨10.1021/acs.organomet.8b00740⟩
Organometallics, 2018, 37 (21), pp.4156-4171. ⟨10.1021/acs.organomet.8b00740⟩
International audience; The complexes FcCH=C{1,4-C≡C-C6H4-C≡CM(dppe)Cp∗}2 (Fc = ferrocenyl (FeCp(η-C5H4-); M = Fe (1), Ru (2)) were prepared from FcCH=C{1,4-C≡C-C6H4-C≡CSiMe3}2 (3) via a desilylation/metalation protocol in good (2; 65%) to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95dac47ba5e83ff9403efe45a954003e
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01939027
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01939027
Autor:
Deanna M. Harrell Moody, Sweta B. Patel, Roger D. Sommer, Thomas C. Coombs, Stacey K. Allen, Thomas E. Lathrop
Publikováno v:
Tetrahedron Letters. 56:6038-6042
Ferrocenium hexafluorophosphate, Cp2FePF6, was determined to be a convenient source of cyclopentadienol when stirred open to air in a mixture of acetonitrile and water. The cyclopentadienol was intercepted via Diels–Alder reaction with a variety of
Publikováno v:
Journal of Molecular Catalysis A: Chemical. 407:221-229
Commercial ferrocenium hexafluorophosphate ([FeCp 2 ]PF 6 ) was found to be an efficient catalyst for the etherification of terminal, tertiary propargylic alcohols with primary and secondary alcohols (5 h to 3 days reaction time at 40 °C in CH 2 Cl
Autor:
Bernd Mühldorf, Christian Müller, Michael Bodensteiner, Babak Rezaei Rad, Uttam Chakraborty, Julian A. W. Sklorz, Robert Wolf
Publikováno v:
Organometallics. 34:622-635
The potassium salt [K([18]crown-6)(THF)2][Cp*Fe(η4-2,4,6-triphenylphosphinine)}] (K1, Cp* = C5Me5) can be isolated in 68% yield by reacting the anionic naphthalene complex [K([18]crown-6){Cp*Fe(η4-C10H8)}] (C10H8 = naphthalene) with 2,4,6-triphenyl