Search Results - "Şeker, Sevil"

  • Showing 1 - 7 results of 7
Refine Results
  1. 1

    Synthesis of rigid and C2-symmetric pyridino-15-crown-5 type macrocycles bearing diamide–diester functions: enantiomeric recognition for chiral primary organoammonium perchlorate salts by Şeker, Sevil, Barış, Deniz, Arslan, Nevin, Turgut, Yılmaz, Pirinççioğlu, Necmettin, Toğrul, Mahmut

    Published in Tetrahedron: asymmetry (15-03-2014)
    “…Four novel C2-symmetric macrocyclic compounds with a pyridine function and possessing amide and ester lingeages were prepared. The enantiomeric discrimination…”
    Get full text
    Journal Article
  2. 2

    A facile synthesis of amide-based receptors under microwave conditions: investigation of their anion recognition properties by experimental and computational tools by Öztürk, Gülşen, Subari, Salih, Şeker, Sevil, Toğrul, Mahmut, Kocakay, Şafak Özhan, Ercan, Selami, Pirinççioğlu, Necmettin

    Published in Journal of molecular modeling (01-09-2017)
    “…Two novel amide-based receptors were synthesized under microwave irradiation. Their chemical structures were confirmed by IR, 1 H NMR, 13 C NMR, and elemental…”
    Get full text
    Journal Article
  3. 3
  4. 4
  5. 5

    Synthesis of rigid and C 2-symmetric 18-crown-6 type macrocycles bearing diamide–diester groups: enantiomeric recognition for α-(1-naphthyl)ethylammonium perchlorate salts by Barış, Deniz, Şeker, Sevil, Hoşgören, Halil, Toğrul, Mahmut

    Published in Tetrahedron: asymmetry (2010)
    “…A series of rigid and chiral C 2-symmetric 18-crown-6 type macrocycles ( S, S)- 4, ( S, S)- 5, ( S, S)- 6 and ( R, R)- 2 bearing diamide–ester groups were…”
    Get full text
    Journal Article
  6. 6
  7. 7

    Asymmetric transfer hydrogenation of acetophenone derivatives with novel chiral phosphinite based η 6- p-cymene/ruthenium(II) catalysts by Aydemir, Murat, Meric, Nermin, Baysal, Akin, Turgut, Yilmaz, Kayan, Cezmi, Şeker, Sevil, Toğrul, Mahmut, Gümgüm, Bahattin

    “…Enantioselective reduction of prochiral ketones to optically active secondary alcohols is an important subject in synthetic organic chemistry because the…”
    Get full text
    Journal Article