Search results

  1. 1.
    0499650 - ÚOCHB 2019 RIV eng P - Patent Document
    Beier, Petr
    Process for the preparation of 3- and 4-(pentafluorosulfanyl)benzenes.
    2018. Owner: Ústav organické chemie a biochemie AV ČR, v. v. i. Date of the patent acceptance: 21.02.2018. Patent Number: EP2625164
    Institutional support: RVO:61388963
    Keywords : pentafluorosulfanyl group * nucleophilic aromatic substitution * nitrobenzenes
    OECD category: Organic chemistry
    https://worldwide.espacenet.com/publicationDetails/originalDocument?FT=D&date=20180221&DB=&locale=en_EP&CC=EP&NR=2625164B1&KC=B1&ND=4#
    Permanent Link: http://hdl.handle.net/11104/0292015
     
     
  2. 2.
    0471199 - ÚOCHB 2017 CZ eng A - Abstract
    Khutorianskyi, Viktor V. - Beier, Petr
    Oxidative nucleophilic aromatic functionalization of nitrobenzenes with nitrogen and oxygen nucleophiles.
    Liblice 2016. 51st Advances in Organic, Bioorganic and Pharmaceutical Chemistry. Praha: Czech Chemical Society, 2016. s. 92.
    [Liblice 2016. Advances in Organic, Bioorganic and Pharmaceutical Chemistry /51./. 11.11.2016-13.11.2016, Lázně Bělohrad]
    Institutional support: RVO:61388963
    Keywords : nitrobenzenes * nucleophiles * nucleophilic amination
    Subject RIV: CC - Organic Chemistry
    Permanent Link: http://hdl.handle.net/11104/0268768
     
     
  3. 3.
    0377816 - ÚOCHB 2013 RIV cze, eng P - Patent Document
    Beier, Petr
    Způsob přípravy substituovaných 3- a 4-(pentafluorsulfanyl)benzenů.
    [Process for preparing substituted 3- and 4-(pentafluorosulfanyl)benzenes.]
    2012. Owner: Ústav organické chemie a biochemie AV ČR v. v. i. Date of the patent acceptance: 04.01.2012. Patent Number: 303004
    Institutional research plan: CEZ:AV0Z40550506
    Keywords : pentafluorosulfanyl group * nucleophilic aromatic substitution * nitrobenzenes
    Subject RIV: CC - Organic Chemistry
    http://spisy.upv.cz/Patents/FullDocuments/303/303004.pdf
    Permanent Link: http://hdl.handle.net/11104/0209869
     
     
  4. 4.
    0360966 - ÚOCHB 2012 RIV US eng J - Journal Article
    Beier, Petr - Pastýříková, Tereza - Vida, Norbert - Iakobson, George
    SNAr Reactions of Nitro-(pentafluorosulfanyl)benzenes To Generate SF5 Aryl Ethers and Sulfides.
    Organic Letters. Roč. 13, č. 6 (2011), s. 1466-1469. ISSN 1523-7060. E-ISSN 1523-7052
    Institutional research plan: CEZ:AV0Z40550506
    Keywords : sulfur pentafluorides * nucleophilic aromatic substitution * nitrobenzenes
    Subject RIV: CC - Organic Chemistry
    Impact factor: 5.862, year: 2011
    Permanent Link: http://hdl.handle.net/11104/0198397
     
     
  5. 5.
    0360936 - ÚOCHB 2012 RIV US eng J - Journal Article
    Beier, Petr - Pastýříková, Tereza - Iakobson, George
    Preparation of SF5 Aromatics by Vicarious Nucleophilic Substitution Reactions of Nitro(pentafluorosulfanyl)benzenes with Carbanions.
    Journal of Organic Chemistry. Roč. 76, č. 11 (2011), s. 4781-4786. ISSN 0022-3263. E-ISSN 1520-6904
    Institutional research plan: CEZ:AV0Z40550506
    Keywords : sulfur pentafluorides * vicarious nucleophilic aromatic substitution * nitrobenzenes
    Subject RIV: CC - Organic Chemistry
    Impact factor: 4.450, year: 2011
    Permanent Link: http://hdl.handle.net/11104/0198373
     
     
  6. 6.
    0097059 - ÚFCH JH 2008 RIV CZ cze C - Conference Paper (international conference)
    Liška, A. - Ludvík, Jiří
    Elektrochemický výzkum intramolekulárních elektronických interakcí a substituovaných nitrobenzenů.
    [Electrochemical investigation of intramolecular electronic interactions in substituted nitrobenzens.]
    Sborník přednášek z XXVII. mezinárodního odborného semináře. Praha: Česká společnost chemická, 2007 - (Barek, J.; Navrátil, T.), s. 77-79. ISBN 978-80-86238-05-0.
    [Moderní elektrochemické metody /27./. Jetřichovice (CZ), 21.05.2007-24.05.2007]
    Institutional research plan: CEZ:AV0Z40400503
    Keywords : electrochemistry * intramolecular electronic interactions * nitrobenzenes
    Subject RIV: CG - Electrochemistry
    Permanent Link: http://hdl.handle.net/11104/0156288
     
     


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