{"_buckets": {"deposit": "3c8cb6b2-0d2a-47d5-83f3-c639bb22334d"}, "_deposit": {"id": "51", "owners": [], "pid": {"revision_id": 0, "type": "depid", "value": "51"}, "status": "published"}, "_oai": {"id": "oai:repository.dl.itc.u-tokyo.ac.jp:00000051"}, "item_2_biblio_info_7": {"attribute_name": "\u66f8\u8a8c\u60c5\u5831", "attribute_value_mlt": [{"bibliographicIssueDates": {"bibliographicIssueDate": "2005-05-30", "bibliographicIssueDateType": "Issued"}, "bibliographicIssueNumber": "22", "bibliographicPageEnd": "3904", "bibliographicPageStart": "3901", "bibliographicVolumeNumber": "46", "bibliographic_titles": [{"bibliographic_title": "Tetrahedron Letters"}]}]}, "item_2_description_13": {"attribute_name": "\u30d5\u30a9\u30fc\u30de\u30c3\u30c8", "attribute_value_mlt": [{"subitem_description": "application/pdf", "subitem_description_type": "Other"}]}, "item_2_description_5": {"attribute_name": "\u6284\u9332", "attribute_value_mlt": [{"subitem_description": "Crown ether-type macrocycles consisting of an enantiopure biarenol derivative and an oligoethylene glycol were synthesized by the lewis acid-mediated tandem Claisen rearrangement.  This is the first example of the successful application of the tandem Claisen rearrangement to the synthesis of enantiopure macrocyclic biarenol derivatives.  The enantiopure macrocyclic biarenols were found to form 1:1 complexes with amino acid salts and to discriminate their chirality.", "subitem_description_type": "Abstract"}]}, "item_2_publisher_20": {"attribute_name": "\u51fa\u7248\u8005", "attribute_value_mlt": [{"subitem_publisher": "Elsevier"}]}, "item_2_relation_11": {"attribute_name": "DOI", "attribute_value_mlt": [{"subitem_relation_type_id": {"subitem_relation_type_id_text": "info:doi/10.1016/j.tetlet.2005.03.167", "subitem_relation_type_select": "DOI"}}]}, "item_2_relation_25": {"attribute_name": "\u95a2\u4fc2URI", "attribute_value_mlt": [{"subitem_relation_type_id": {"subitem_relation_type_id_text": "http://www.elsevier.com/locate/issn/00404039", "subitem_relation_type_select": "URI"}}]}, "item_2_select_14": {"attribute_name": "\u8457\u8005\u7248\u30d5\u30e9\u30b0", "attribute_value_mlt": [{"subitem_select_item": "author"}]}, "item_2_source_id_8": {"attribute_name": "ISSN", "attribute_value_mlt": [{"subitem_source_identifier": "00404039", "subitem_source_identifier_type": "ISSN"}]}, "item_2_text_34": {"attribute_name": "\u8cc7\u6e90\u30bf\u30a4\u30d7", "attribute_value_mlt": [{"subitem_text_value": "Journal Article"}]}, "item_creator": {"attribute_name": "\u8457\u8005", "attribute_type": "creator", "attribute_value_mlt": [{"creatorNames": [{"creatorName": "Saigo, Kazuhiko"}], "nameIdentifiers": [{"nameIdentifier": "105781", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Yoshida, Hiroaki"}], "nameIdentifiers": [{"nameIdentifier": "105782", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Kobayashia, Yuka"}], "nameIdentifiers": [{"nameIdentifier": "105783", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Hiratani, Kazuhisa"}], "nameIdentifiers": [{"nameIdentifier": "105784", "nameIdentifierScheme": "WEKO"}]}]}, "item_files": {"attribute_name": "\u30d5\u30a1\u30a4\u30eb\u60c5\u5831", "attribute_type": "file", "attribute_value_mlt": [{"accessrole": "open_date", "date": [{"dateType": "Available", "dateValue": "2017-06-26"}], "displaytype": "detail", "download_preview_message": "", "file_order": 0, "filename": "12_Elsevier_w.pdf", "filesize": [{"value": "129.9 kB"}], "format": "application/pdf", "future_date_message": "", "is_thumbnail": false, "licensetype": "license_free", "mimetype": "application/pdf", "size": 129900.0, "url": {"label": "12_Elsevier_w.pdf", "url": "https://repository.dl.itc.u-tokyo.ac.jp/record/51/files/12_Elsevier_w.pdf"}, "version_id": "5c9156e6-9e18-4f8f-af25-66bfa77fa320"}]}, "item_keyword": {"attribute_name": "\u30ad\u30fc\u30ef\u30fc\u30c9", "attribute_value_mlt": [{"subitem_subject": "Tandem Claisen rearrangement", "subitem_subject_scheme": "Other"}, {"subitem_subject": "1,1\u2032-Bi-2-naphthol", "subitem_subject_scheme": "Other"}, {"subitem_subject": "Chiral recognition", "subitem_subject_scheme": "Other"}, {"subitem_subject": "Host?guest complex", "subitem_subject_scheme": "Other"}, {"subitem_subject": "Amino acid salt", "subitem_subject_scheme": "Other"}]}, "item_language": {"attribute_name": "\u8a00\u8a9e", "attribute_value_mlt": [{"subitem_language": "eng"}]}, "item_resource_type": {"attribute_name": "\u8cc7\u6e90\u30bf\u30a4\u30d7", "attribute_value_mlt": [{"resourcetype": "journal article", "resourceuri": "http://purl.org/coar/resource_type/c_6501"}]}, "item_title": "Synthesis and properties of macrocyclic 1,1\u2019-biarenol derivatives prepared by the tandem Claisen rearrangement", "item_titles": {"attribute_name": "\u30bf\u30a4\u30c8\u30eb", "attribute_value_mlt": [{"subitem_title": "Synthesis and properties of macrocyclic 1,1\u2019-biarenol derivatives prepared by the tandem Claisen rearrangement"}]}, "item_type_id": "2", "owner": "1", "path": ["9/10/11", "6/18/19"], "permalink_uri": "http://hdl.handle.net/2261/6004", "pubdate": {"attribute_name": "\u516c\u958b\u65e5", "attribute_name_i18n": "\u516c\u958b\u65e5", "attribute_value": "2007-05-10"}, "publish_date": "2007-05-10", "publish_status": "0", "recid": "51", "relation": {}, "relation_version_is_last": true, "title": ["Synthesis and properties of macrocyclic 1,1\u2019-biarenol derivatives prepared by the tandem Claisen rearrangement"], "weko_shared_id": null}