يعرض 1 - 20 نتائج من 109 نتيجة بحث عن '"4-oxadiazoles"', وقت الاستعلام: 0.65s تنقيح النتائج
  1. 1
    Dissertation/ Thesis

    المؤلفون: Jos, Swetha

    Thesis Advisors: Chemistry, Santos, Webster L., Lowell, Andrew Nesemann, Carlier, Paul R., Schulz, Michael

    مصطلحات موضوعية: Trifluoromethylation, Organocatalysis, Enynes, Enamides, 1, 2, 4-Oxadiazoles

    وصف الملف: ETD; application/pdf

  2. 2
    Academic Journal

    المصدر: Pharmacia, 70((4)), 1093-1100, (2023-10-12)

    Time: 1, 3

    Relation: https://doi.org/10.3897/pharmacia.70.e102449.scheme1; https://doi.org/10.1002/jhet.3906; https://doi.org/10.5267/j.ccl.2020.11.002; https://doi.org/10.1080/14756366.2020.1759581; https://doi.org/10.1016/j.bioorg.2018.10.025; https://doi.org/10.1016/j.ejmech.2011.12.013; https://doi.org/10.1002/ddr.430340203; https://doi.org/10.1007/978-1-4615-8152-9_2; https://doi.org/10.1016/S0968-0896(01)00366-2; https://doi.org/10.1007/s00044-018-02288-z; https://doi.org/10.1016/j.bmcl.2005.05.034; https://doi.org/10.1016/j.bmcl.2015.09.051; https://doi.org/10.1021/jm8004306; https://doi.org/10.1016/j.bmc.2013.01.029; https://doi.org/10.1016/j.bmc.2010.07.067; https://doi.org/10.1002/ardp.201300231; https://doi.org/10.33263/BRIAC104.960971; https://doi.org/10.5267/j.ccl.2022.11.005; https://doi.org/10.23939/chcht09.01.029; https://doi.org/10.7324/JAPS.2020.1010016; https://doi.org/10.33263/BRIAC125.67106722; https://doi.org/10.33263/BRIAC121.11611173; https://doi.org/10.1016/j.bmcl.2010.11.041; https://doi.org/10.1093/jnci/83.11.757; https://doi.org/10.1007/s11164-017-2953-0; https://doi.org/10.1016/j.bioorg.2020.103657; https://doi.org/10.1016/j.bmcl.2008.03.013; https://doi.org/10.1016/j.ejmech.2010.07.014; https://doi.org/10.1016/j.bmcl.2011.08.022; https://doi.org/10.1002/ardp.200700146; https://doi.org/10.1016/j.ejmech.2015.02.053; https://doi.org/10.1016/j.bmcl.2007.04.110; https://doi.org/10.1016/j.ejmech.2013.02.030; https://doi.org/10.1080/00397911.2017.1360911; https://doi.org/10.1038/nrc1951; https://doi.org/10.1016/j.molstruc.2020.128847; https://doi.org/10.1016/j.bmc.2019.115047; https://doi.org/10.1002/ardp.202000342; https://doi.org/10.1016/j.bioorg.2020.104276; https://doi.org/10.1016/j.ejmech.2013.11.017; https://doi.org/10.1007/s11030-020-10087-1; https://doi.org/10.1111/cbdd.13795; https://doi.org/10.1016/j.bmc.2008.02.001; https://doi.org/10.1517/13543776.2013.797409; https://doi.org/10.1016/j.bmc.2013.04.043; https://doi.org/10.1016/j.bmc.2012.08.059; https://doi.org/10.3897/pharmacia.70.e102449; oai:zenodo.org:10411966

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    Academic Journal

    المساهمون: Department of Chemistry

    Time: 2, 3

    وصف الملف: application/octet-stream

    Relation: Support by the KIT-Publication Fund of the Karlsruhe Institute of Technology.; Aly , A A , Bräse , S , Hassan , A A , Mohamed , N K , Abd El-Haleem , L E & Nieger , M 2020 , ' Synthesis of New Planar-Chiral Linked [2.2]Paracyclophanes-N-([2.2]-Paracyclophanylcarbamoyl)-4-([2.2]Paracyclophanylcarboxamide, [2.2]Paracyclophanyl-Substituted Triazolthiones and -Substituted Oxadiazoles ' , Molecules , vol. 25 , no. 15 , 3315 . https://doi.org/10.3390/molecules25153315; ORCID: /0000-0003-1677-0109/work/80943539; http://hdl.handle.net/10138/319602; 90831f00-e7c3-45e7-b7ac-641505893108; 000567088400001

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