{"created":"2023-05-15T11:43:17.674221+00:00","id":2950,"links":{},"metadata":{"_buckets":{"deposit":"ab38479d-70da-429e-8552-09b2aacd63ec"},"_deposit":{"created_by":1,"id":"2950","owners":[1],"pid":{"revision_id":0,"type":"depid","value":"2950"},"status":"published"},"_oai":{"id":"oai:kanagawa-u.repo.nii.ac.jp:00002950","sets":["237:238:239"]},"author_link":["5973","5966","5968","5971","5969","5970","5967","5972"],"item_7_biblio_info_7":{"attribute_name":"書誌情報","attribute_value_mlt":[{"bibliographicIssueDates":{"bibliographicIssueDate":"1984-09","bibliographicIssueDateType":"Issued"},"bibliographicIssueNumber":"9","bibliographicPageEnd":"2542","bibliographicPageStart":"2538","bibliographicVolumeNumber":"57","bibliographic_titles":[{"bibliographic_title":"Bulletin of the Chemical Society of Japan"}]}]},"item_7_description_4":{"attribute_name":"抄録","attribute_value_mlt":[{"subitem_description":"The title compound was synthesized from methyl 4-O-benzyl-2,6-dideoxy-β-L-threo-hexopyranosid-3-ulose (19) through cyanomesylation, reductive spiro aziridine formation, and reductive ring-opening. When (2-methoxyethoxymethyl) group was used as the protecting group at O-4 of the above intermediate, it could not be removed at the final stage.","subitem_description_type":"Abstract"}]},"item_7_description_40":{"attribute_name":"資源タイプ","attribute_value_mlt":[{"subitem_description":"Article","subitem_description_type":"Other"}]},"item_7_publisher_33":{"attribute_name":"出版者","attribute_value_mlt":[{"subitem_publisher":"日本化学会"}]},"item_7_relation_12":{"attribute_name":"DOI","attribute_value_mlt":[{"subitem_relation_type":"isIdenticalTo","subitem_relation_type_id":{"subitem_relation_type_id_text":"10.1246/bcsj.57.2538","subitem_relation_type_select":"DOI"}}]},"item_7_source_id_10":{"attribute_name":"書誌レコードID","attribute_value_mlt":[{"subitem_source_identifier":"AA00580132","subitem_source_identifier_type":"NCID"}]},"item_7_source_id_8":{"attribute_name":"ISSN","attribute_value_mlt":[{"subitem_source_identifier":"0009-2673","subitem_source_identifier_type":"ISSN"}]},"item_7_version_type_16":{"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":"安盛, 俊雄"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Yasumori, Toshio"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"佐藤, 憲一"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Sato, Ken-ichi"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"橋本, 弘信"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Hashimoto, Hironobu"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"吉村, 寿次"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Yoshimura, Juji"}],"nameIdentifiers":[{}]}]},"item_files":{"attribute_name":"ファイル情報","attribute_type":"file","attribute_value_mlt":[{"accessrole":"open_date","date":[{"dateType":"Available","dateValue":"2018-11-16"}],"displaytype":"detail","filename":"佐藤・化学-016.pdf","filesize":[{"value":"3.9 MB"}],"format":"application/pdf","licensetype":"license_note","mimetype":"application/pdf","url":{"label":"佐藤・化学-016.pdf","url":"https://kanagawa-u.repo.nii.ac.jp/record/2950/files/佐藤・化学-016.pdf"},"version_id":"fa151bc0-57e5-4e15-9b36-548b05384893"}]},"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":"journal article","resourceuri":"http://purl.org/coar/resource_type/c_6501"}]},"item_title":"Branched-chain Sugars. XXXVI. A New Synthesis of Methyl 4-O-Benzoyl-3-benzoylamino-2,3,6-trideoxy-3-C-methyl-α-L-xylo-hexopyranoside, a Derivative of the Branched-chain Amino Sugar of Antibiotic A35512B","item_titles":{"attribute_name":"タイトル","attribute_value_mlt":[{"subitem_title":"Branched-chain Sugars. XXXVI. A New Synthesis of Methyl 4-O-Benzoyl-3-benzoylamino-2,3,6-trideoxy-3-C-methyl-α-L-xylo-hexopyranoside, a Derivative of the Branched-chain Amino Sugar of Antibiotic A35512B"}]},"item_type_id":"7","owner":"1","path":["239"],"pubdate":{"attribute_name":"公開日","attribute_value":"2011-01-28"},"publish_date":"2011-01-28","publish_status":"0","recid":"2950","relation_version_is_last":true,"title":["Branched-chain Sugars. XXXVI. A New Synthesis of Methyl 4-O-Benzoyl-3-benzoylamino-2,3,6-trideoxy-3-C-methyl-α-L-xylo-hexopyranoside, a Derivative of the Branched-chain Amino Sugar of Antibiotic A35512B"],"weko_creator_id":"1","weko_shared_id":-1},"updated":"2023-05-15T16:35:02.072850+00:00"}