{"created":"2023-06-19T09:18:35.294559+00:00","id":31545,"links":{},"metadata":{"_buckets":{"deposit":"c887d3b8-c839-4aca-a588-fb2ca36d80fa"},"_deposit":{"created_by":1,"id":"31545","owners":[1],"pid":{"revision_id":0,"type":"depid","value":"31545"},"status":"published"},"_oai":{"id":"oai:kumadai.repo.nii.ac.jp:00031545","sets":["448:449"]},"author_link":["146758","146621","146616","146618","146620","146622","146617","146619"],"item_23_biblio_info_6":{"attribute_name":"書誌情報","attribute_value_mlt":[{"bibliographicIssueDates":{"bibliographicIssueDate":"2019-05-20","bibliographicIssueDateType":"Issued"},"bibliographicPageEnd":"5751","bibliographicPageStart":"5737","bibliographicVolumeNumber":"43","bibliographic_titles":[{"bibliographic_title":"New Journal of Chemistry"}]}]},"item_23_creator_3":{"attribute_name":"別言語の著者","attribute_type":"creator","attribute_value_mlt":[{"creatorAffiliations":[{"affiliationNameIdentifiers":[{"affiliationNameIdentifier":"","affiliationNameIdentifierScheme":"ISNI","affiliationNameIdentifierURI":"http://www.isni.org/isni/"}],"affiliationNames":[{"affiliationName":"","affiliationNameLang":"ja"}]}],"creatorNames":[{"creatorName":"Nishino, Hiroshi","creatorNameLang":"en"},{"creatorName":"西野, 宏","creatorNameLang":"ja"},{"creatorName":"ニシノ, ヒロシ","creatorNameLang":"ja-Kana"}],"familyNames":[{"familyName":"Nishino","familyNameLang":"en"},{"familyName":"西野","familyNameLang":"ja"},{"familyName":"ニシノ","familyNameLang":"ja-Kana"}],"givenNames":[{"givenName":"Hiroshi","givenNameLang":"en"},{"givenName":"宏","givenNameLang":"ja"},{"givenName":"ヒロシ","givenNameLang":"ja-Kana"}],"nameIdentifiers":[{"nameIdentifier":"146758","nameIdentifierScheme":"WEKO"}]}]},"item_23_description_5":{"attribute_name":"内容記述","attribute_value_mlt":[{"subitem_description":"The syntheses of new series of pyranones, namely fused pyranones and quinoline-based dihydrofurans accompanied by 3-alkenyl-substituted structures were described. The products were regioselectively formed Mn(III)-mediated oxidation at elevated temperature in order to obtain excellent yields. The effects on product distributions of the thiophene group together with the temperatures and reactions time were investigated. The structures of the syntheses compounds were determined on the basis of spectroscopic (IR, 1H NMR, 13C NMR, COSY, HSQC, HMBC and elemental analysis) and X-ray crystallographic data.\nIn addition, the in vitro antimicrobial activities of the some syntheses dihydrofurans were tested against G (+) and G (-) bacteria using disc diffusion method. The results indicated that the compounds containing  thiophene group showed a better antimicrobial effect than some commonly used antibiotics.","subitem_description_type":"Other"}]},"item_23_description_77":{"attribute_name":"URL","attribute_value_mlt":[{"subitem_description":"https://pubs.rsc.org/en/content/articlelanding/2019/nj/c9nj00054b#!divAbstract","subitem_description_type":"Other"}]},"item_23_publisher_36":{"attribute_name":"出版者","attribute_value_mlt":[{"subitem_publisher":"Royal Society of Chemistry"}]},"item_23_relation_11":{"attribute_name":"DOI","attribute_value_mlt":[{"subitem_relation_type":"isVersionOf","subitem_relation_type_id":{"subitem_relation_type_id_text":"10.1039/C9NJ00054B","subitem_relation_type_select":"DOI"}}]},"item_23_source_id_7":{"attribute_name":"ISSN","attribute_value_mlt":[{"subitem_source_identifier":"11440546","subitem_source_identifier_type":"ISSN"}]},"item_23_subject_20":{"attribute_name":"日本十進分類法","attribute_value_mlt":[{"subitem_subject":"438","subitem_subject_scheme":"NDC"}]},"item_23_text_47":{"attribute_name":"資源タイプ・ローカル","attribute_value_mlt":[{"subitem_text_value":"プレプリント"}]},"item_23_text_48":{"attribute_name":"資源タイプ・NII","attribute_value_mlt":[{"subitem_text_value":"Preprint"}]},"item_23_text_49":{"attribute_name":"資源タイプ・DCMI","attribute_value_mlt":[{"subitem_text_value":"text"}]},"item_23_text_50":{"attribute_name":"資源タイプ・ローカル表示コード","attribute_value_mlt":[{"subitem_text_value":"01"}]},"item_23_version_type_19":{"attribute_name":"著者版フラグ","attribute_value_mlt":[{"subitem_version_resource":"http://purl.org/coar/version/c_b1a7d7d4d402bcce","subitem_version_type":"AO"}]},"item_creator":{"attribute_name":"著者","attribute_type":"creator","attribute_value_mlt":[{"creatorAffiliations":[{"affiliationNameIdentifiers":[{"affiliationNameIdentifier":"","affiliationNameIdentifierScheme":"ISNI","affiliationNameIdentifierURI":"http://www.isni.org/isni/"}],"affiliationNames":[{"affiliationName":"","affiliationNameLang":"ja"}]}],"creatorNames":[{"creatorName":"Özgür, Mehtap","creatorNameLang":"en"}],"familyNames":[{"familyName":"Özgür","familyNameLang":"en"}],"givenNames":[{"givenName":"Mehtap","givenNameLang":"en"}],"nameIdentifiers":[{"nameIdentifier":"146616","nameIdentifierScheme":"WEKO"}]},{"creatorNames":[{"creatorName":"Yılmaz, Mehmet"}],"nameIdentifiers":[{"nameIdentifier":"146617","nameIdentifierScheme":"WEKO"}]},{"creatorNames":[{"creatorName":"Nishino, Hiroshi"}],"nameIdentifiers":[{"nameIdentifier":"146618","nameIdentifierScheme":"WEKO"}]},{"creatorAffiliations":[{"affiliationNameIdentifiers":[{"affiliationNameIdentifier":"","affiliationNameIdentifierScheme":"ISNI","affiliationNameIdentifierURI":"http://www.isni.org/isni/"}],"affiliationNames":[{"affiliationName":"","affiliationNameLang":"ja"}]}],"creatorNames":[{"creatorName":"Çinar, Eda","creatorNameLang":"en"}],"familyNames":[{"familyName":"Çinar","familyNameLang":"en"}],"givenNames":[{"givenName":"Eda","givenNameLang":"en"}],"nameIdentifiers":[{"nameIdentifier":"146619","nameIdentifierScheme":"WEKO"}]},{"creatorNames":[{"creatorName":"Dal, Hakan"}],"nameIdentifiers":[{"nameIdentifier":"146620","nameIdentifierScheme":"WEKO"}]},{"creatorNames":[{"creatorName":"Pekel, A.Tarık"}],"nameIdentifiers":[{"nameIdentifier":"146621","nameIdentifierScheme":"WEKO"}]},{"creatorNames":[{"creatorName":"Hökelek, Tuncer"}],"nameIdentifiers":[{"nameIdentifier":"146622","nameIdentifierScheme":"WEKO"}]}]},"item_files":{"attribute_name":"ファイル情報","attribute_type":"file","attribute_value_mlt":[{"accessrole":"open_date","date":[{"dateType":"Available","dateValue":"2020-03-03"}],"displaytype":"detail","filename":"NJC-2019-reposit.pdf","filesize":[{"value":"13.6 MB"}],"format":"application/pdf","licensetype":"license_note","mimetype":"application/pdf","url":{"label":"NJC-2019-reposit","url":"https://kumadai.repo.nii.ac.jp/record/31545/files/NJC-2019-reposit.pdf"},"version_id":"b2d8a0da-a62d-400d-b732-5c88dc40a297"}]},"item_keyword":{"attribute_name":"キーワード","attribute_value_mlt":[{"subitem_subject":"manganese(III) acetate","subitem_subject_scheme":"Other"},{"subitem_subject":"dihydrofuran","subitem_subject_scheme":"Other"},{"subitem_subject":"3-alkenyl–substituted coumarin","subitem_subject_scheme":"Other"},{"subitem_subject":"antimicrobial activity","subitem_subject_scheme":"Other"},{"subitem_subject":"thiophene","subitem_subject_scheme":"Other"}]},"item_language":{"attribute_name":"言語","attribute_value_mlt":[{"subitem_language":"eng"}]},"item_resource_type":{"attribute_name":"資源タイプ","attribute_value_mlt":[{"resourcetype":"other","resourceuri":"http://purl.org/coar/resource_type/c_1843"}]},"item_title":"Efficient Syntheses and Antimicrobial Activities of New Thiophene Containing Pyranone and Quinolinone Derivatives by Manganese(III) Acetate. The effect of Thiophene on Ring Closure- Opening Reactions","item_titles":{"attribute_name":"タイトル","attribute_value_mlt":[{"subitem_title":"Efficient Syntheses and Antimicrobial Activities of New Thiophene Containing Pyranone and Quinolinone Derivatives by Manganese(III) Acetate. The effect of Thiophene on Ring Closure- Opening Reactions"}]},"item_type_id":"23","owner":"1","path":["449"],"pubdate":{"attribute_name":"公開日","attribute_value":"2020-05-21"},"publish_date":"2020-05-21","publish_status":"0","recid":"31545","relation_version_is_last":true,"title":["Efficient Syntheses and Antimicrobial Activities of New Thiophene Containing Pyranone and Quinolinone Derivatives by Manganese(III) Acetate. The effect of Thiophene on Ring Closure- Opening Reactions"],"weko_creator_id":"1","weko_shared_id":1},"updated":"2023-08-21T07:25:46.625879+00:00"}