{"created":"2023-06-20T13:11:23.680022+00:00","id":587,"links":{},"metadata":{"_buckets":{"deposit":"8bbffc97-2977-4f27-b71e-a53a2502bb15"},"_deposit":{"created_by":15,"id":"587","owners":[15],"pid":{"revision_id":0,"type":"depid","value":"587"},"status":"published"},"_oai":{"id":"oai:tohoku-mpu.repo.nii.ac.jp:00000587","sets":["3:43"]},"author_link":[],"item_10002_biblio_info_7":{"attribute_name":"書誌情報","attribute_value_mlt":[{"bibliographicIssueDates":{"bibliographicIssueDate":"2014-12","bibliographicIssueDateType":"Issued"},"bibliographicIssueNumber":"61","bibliographicPageEnd":"33","bibliographicPageStart":"27","bibliographic_titles":[{"bibliographic_title":"東北薬科大学研究誌","bibliographic_titleLang":"ja"},{"bibliographic_title":"Journal of Tohoku Pharmaceutical University","bibliographic_titleLang":"en"}]}]},"item_10002_description_5":{"attribute_name":"抄録","attribute_value_mlt":[{"subitem_description":"A novel synthesis of naphtoh［2,1-d］oxazol-5-ol, a model compound for the benzoxazole moiety of marine natural products nakijinols A and B, was achieved in five steps in 35% overall yield starting from commercially available 2-methoxy-1,4-naphthoquinone. The synthesis involved the following crucial steps: ⅰ reduction of an N-Boc-protected 2-amino-1,4-naphthoquione; ⅱ protection of the resulting 2-aminohydronaphthoquinone as its diformate form; ⅲ a simultaneous N-Boc-deprotection and cyclization of the resulting diformate to construct an oxazole ring.","subitem_description_language":"en","subitem_description_type":"Abstract"}]},"item_10002_publisher_8":{"attribute_name":"出版者","attribute_value_mlt":[{"subitem_publisher":"東北薬科大学","subitem_publisher_language":"ja"}]},"item_10002_rights_15":{"attribute_name":"権利","attribute_value_mlt":[{"subitem_rights":"Attribution-NonCommercial-NoDerivs 3.0 Unported (CC BY-NC-ND 3.0)","subitem_rights_language":"en","subitem_rights_resource":"https://creativecommons.org/licenses/by-nc-nd/3.0/deed.en"}]},"item_10002_source_id_11":{"attribute_name":"書誌レコードID","attribute_value_mlt":[{"subitem_source_identifier":"AA1149311X","subitem_source_identifier_type":"NCID"}]},"item_10002_source_id_9":{"attribute_name":"ISSN","attribute_value_mlt":[{"subitem_source_identifier":"1345-157X","subitem_source_identifier_type":"PISSN"}]},"item_10002_version_type_20":{"attribute_name":"著者版フラグ","attribute_value_mlt":[{"subitem_version_resource":"http://purl.org/coar/version/c_970fb48d4fbd8a85","subitem_version_type":"VoR"}]},"item_creator":{"attribute_name":"著者","attribute_type":"creator","attribute_value_mlt":[{"creatorNames":[{"creatorName":"加藤, 武","creatorNameLang":"ja"},{"creatorName":"カトウ, タケル","creatorNameLang":"ja-Kana"},{"creatorName":"Katoh, Takeru","creatorNameLang":"en"}]},{"creatorNames":[{"creatorName":"佐藤, 廣河","creatorNameLang":"ja"},{"creatorName":"サトウ, ヒロカ","creatorNameLang":"ja-Kana"},{"creatorName":"Satoh, Hiroka","creatorNameLang":"en"}]},{"creatorNames":[{"creatorName":"平間, 美佳","creatorNameLang":"ja"},{"creatorName":"ヒラマ, ミカ","creatorNameLang":"ja-Kana"},{"creatorName":"Hirama, Mika","creatorNameLang":"en"}]},{"creatorNames":[{"creatorName":"熱海, 秀","creatorNameLang":"ja"},{"creatorName":"アツミ, スグル","creatorNameLang":"ja-Kana"},{"creatorName":"Atsumi, Suguru","creatorNameLang":"en"}]},{"creatorNames":[{"creatorName":"成田, 紘一","creatorNameLang":"ja"},{"creatorName":"ナリタ, コウイチ","creatorNameLang":"ja-Kana"},{"creatorName":"Narita, Koichi","creatorNameLang":"en"}]},{"creatorNames":[{"creatorName":"加藤, 正","creatorNameLang":"ja"},{"creatorName":"カトウ, タダシ","creatorNameLang":"ja-Kana"},{"creatorName":"Katoh, Tadashi","creatorNameLang":"en"}]}]},"item_files":{"attribute_name":"ファイル情報","attribute_type":"file","attribute_value_mlt":[{"accessrole":"open_date","date":[{"dateType":"Available","dateValue":"2015-04-23"}],"displaytype":"detail","filename":"61(27−33).pdf","filesize":[{"value":"1.6 MB"}],"format":"application/pdf","licensetype":"license_11","mimetype":"application/pdf","url":{"label":"o -アミノフェノールのギ酸エステル誘導体を用いたo -アミノフェノールのギ酸エステル誘導体を用いたo -アミノフェノールのギ酸エステル誘導体を用いたベンゾオキサゾール環構築法の開発","objectType":"fulltext","url":"https://tohoku-mpu.repo.nii.ac.jp/record/587/files/61(27−33).pdf"},"version_id":"65fa0620-caba-4b62-a524-5ef6c6dd35c5"}]},"item_keyword":{"attribute_name":"キーワード","attribute_value_mlt":[{"subitem_subject":"nakijinol A and B","subitem_subject_language":"en","subitem_subject_scheme":"Other"},{"subitem_subject":"marine natural product","subitem_subject_language":"en","subitem_subject_scheme":"Other"},{"subitem_subject":"anticancer agent","subitem_subject_language":"en","subitem_subject_scheme":"Other"},{"subitem_subject":"benzoxazole ring formation","subitem_subject_language":"en","subitem_subject_scheme":"Other"}]},"item_language":{"attribute_name":"言語","attribute_value_mlt":[{"subitem_language":"jpn"}]},"item_resource_type":{"attribute_name":"資源タイプ","attribute_value_mlt":[{"resourcetype":"departmental bulletin paper","resourceuri":"http://purl.org/coar/resource_type/c_6501"}]},"item_title":"o-アミノフェノールのギ酸エステル誘導体を用いたベンゾオキサゾール環構築法の開発","item_titles":{"attribute_name":"タイトル","attribute_value_mlt":[{"subitem_title":"o-アミノフェノールのギ酸エステル誘導体を用いたベンゾオキサゾール環構築法の開発","subitem_title_language":"ja"},{"subitem_title":"Development of the Method for Construction of Benzoxazole Ring via o-Aminophenyl Formate","subitem_title_language":"en"}]},"item_type_id":"10002","owner":"15","path":["43"],"pubdate":{"attribute_name":"PubDate","attribute_value":"2015-04-23"},"publish_date":"2015-04-23","publish_status":"0","recid":"587","relation_version_is_last":true,"title":["o-アミノフェノールのギ酸エステル誘導体を用いたベンゾオキサゾール環構築法の開発"],"weko_creator_id":"15","weko_shared_id":-1},"updated":"2024-03-03T23:42:48.974694+00:00"}