1 Ocak 2022 Dergi makalesi Açık Erişim

Ahmadli, Dilgam; Sahin, Yesim; Calikyilmaz, Eylul; Sahin, Onur; Turkmen, Yunus E.

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        "affiliation": "Bilkent Univ, Fac Sci, Dept Chem, TR-06800 Ankara, Turkey", 
        "name": "Ahmadli, Dilgam"
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      {
        "affiliation": "Bilkent Univ, Fac Sci, Dept Chem, TR-06800 Ankara, Turkey", 
        "name": "Sahin, Yesim"
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      {
        "affiliation": "Bilkent Univ, Fac Sci, Dept Chem, TR-06800 Ankara, Turkey", 
        "name": "Calikyilmaz, Eylul"
      }, 
      {
        "affiliation": "Sinop Univ, Fac Hlth Sci, Dept Occupat Hlth & Safety, TR-57000 Sinop, Turkey", 
        "name": "Sahin, Onur"
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        "name": "Turkmen, Yunus E."
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    "description": "In this work, we developed an efficient method for the rapid construction of fluoranthene skeleton to access a variety of substituted hydroxyfluoranthenes. The 1-iodo-8-alkynylnaphthalene derivatives, which serve as substrates for the key fluoranthene-forming step, were prepared via selective monoalkynylative Sonogashira reactions of 1,8-diiodonaphthalene. The domino reaction sequence which involves a sequential Suzuki-Miyaura coupling, an intramolecular Diels-Alder reaction, and an aromatization-driven ring-opening isomerization has been shown to give substituted hydroxyfluoranthenes in up to 92% yield. This work demonstrates the utility of designing new domino reactions for rapid access to substituted polycyclic aromatic hydrocarbons (PAHs).", 
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    "journal": {
      "issue": "9", 
      "pages": "6336-6346", 
      "title": "JOURNAL OF ORGANIC CHEMISTRY", 
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    "publication_date": "2022-01-01", 
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    "title": "Rapid Access to Hydroxyfluoranthenes via a Domino Suzuki-Miyaura/Intramolecular Diels-Alder/Ring-Opening Reactions Sequence"
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