Dergi makalesi Açık Erişim

Synthesis of 1-Azaspiro[4.5]deca-1,3-dienes from N-Propargylic beta-Enaminones in Basic Medium

Karadeniz, Eda; Zora, Metin


JSON

{
  "conceptrecid": "70542", 
  "created": "2021-03-16T03:17:00.806415+00:00", 
  "doi": "10.1055/s-0037-1611723", 
  "files": [
    {
      "bucket": "d505898b-2fa3-4daf-b4fc-1fe1c38fffc9", 
      "checksum": "md5:87f151594fc441d13ee900dab78df6df", 
      "key": "bib-4c063ae4-c020-4db7-97e7-ffc0a4765706.txt", 
      "links": {
        "self": "https://aperta.ulakbim.gov.tr/api/files/d505898b-2fa3-4daf-b4fc-1fe1c38fffc9/bib-4c063ae4-c020-4db7-97e7-ffc0a4765706.txt"
      }, 
      "size": 168, 
      "type": "txt"
    }
  ], 
  "id": 70543, 
  "links": {
    "badge": "https://aperta.ulakbim.gov.tr/badge/doi/10.1055/s-0037-1611723.svg", 
    "bucket": "https://aperta.ulakbim.gov.tr/api/files/d505898b-2fa3-4daf-b4fc-1fe1c38fffc9", 
    "doi": "https://doi.org/10.1055/s-0037-1611723", 
    "html": "https://aperta.ulakbim.gov.tr/record/70543", 
    "latest": "https://aperta.ulakbim.gov.tr/api/records/70543", 
    "latest_html": "https://aperta.ulakbim.gov.tr/record/70543"
  }, 
  "metadata": {
    "access_right": "open", 
    "access_right_category": "success", 
    "communities": [
      {
        "id": "tubitak-destekli-proje-yayinlari"
      }
    ], 
    "creators": [
      {
        "affiliation": "Middle East Tech Univ, Dept Chem, TR-06800 Ankara, Turkey", 
        "name": "Karadeniz, Eda"
      }, 
      {
        "affiliation": "Middle East Tech Univ, Dept Chem, TR-06800 Ankara, Turkey", 
        "name": "Zora, Metin"
      }
    ], 
    "description": "A facile, efficient and unprecedented method for the synthesis of spiro-2H-pyrroles is reported. When reacted with 1-ethynylcyclohexylamine, a, ss-alkynic ketones produced cyclohexane-embedded Npropargylic ss-enaminones, which in the presence of cesium carbonate underwent nucleophilic cyclization to afford 1-azaspiro[ 4.5] deca-1,3diene derivatives in good to excellent yields. This cyclization was found to be general for a variety of cyclohexane-embedded N-propargylic ss enaminones and demonstrated good tolerance to a broad range of aliphatic, aromatic and heteroaromatic groups with electron-withdrawing and electron-donating substituents. The decoration of pyrrole compounds with a spiro framework may exhibit potential for the synthesis of molecules of pharmacological interest.", 
    "doi": "10.1055/s-0037-1611723", 
    "has_grant": false, 
    "journal": {
      "issue": "10", 
      "pages": "2157-2170", 
      "title": "SYNTHESIS-STUTTGART", 
      "volume": "51"
    }, 
    "license": {
      "id": "cc-by"
    }, 
    "publication_date": "2019-01-01", 
    "relations": {
      "version": [
        {
          "count": 1, 
          "index": 0, 
          "is_last": true, 
          "last_child": {
            "pid_type": "recid", 
            "pid_value": "70543"
          }, 
          "parent": {
            "pid_type": "recid", 
            "pid_value": "70542"
          }
        }
      ]
    }, 
    "resource_type": {
      "subtype": "article", 
      "title": "Dergi makalesi", 
      "type": "publication"
    }, 
    "title": "Synthesis of 1-Azaspiro[4.5]deca-1,3-dienes from N-Propargylic beta-Enaminones in Basic Medium"
  }, 
  "owners": [
    1
  ], 
  "revision": 1, 
  "stats": {
    "downloads": 5.0, 
    "unique_downloads": 5.0, 
    "unique_views": 25.0, 
    "version_downloads": 5.0, 
    "version_unique_downloads": 5.0, 
    "version_unique_views": 25.0, 
    "version_views": 26.0, 
    "version_volume": 840.0, 
    "views": 26.0, 
    "volume": 840.0
  }, 
  "updated": "2021-03-16T03:17:00.857285+00:00"
}
26
5
görüntülenme
indirilme
Görüntülenme 26
İndirme 5
Veri hacmi 840 Bytes
Tekil görüntülenme 25
Tekil indirme 5

Alıntı yap