{"created":"2021-03-01T06:32:41.737220+00:00","id":24722,"links":{},"metadata":{"_buckets":{"deposit":"e31299e9-4098-489b-8cc9-3a40fc27e535"},"_deposit":{"id":"24722","owners":[],"pid":{"revision_id":0,"type":"depid","value":"24722"},"status":"published"},"_oai":{"id":"oai:nagoya.repo.nii.ac.jp:00024722","sets":[]},"author_link":["73363","73364","73365"],"item_10_biblio_info_6":{"attribute_name":"\u66f8\u8a8c\u60c5\u5831","attribute_value_mlt":[{"bibliographicIssueDates":{"bibliographicIssueDate":"2017-06-06","bibliographicIssueDateType":"Issued"},"bibliographicIssueNumber":"24","bibliographicPageEnd":"6983","bibliographicPageStart":"6980","bibliographicVolumeNumber":"56","bibliographic_titles":[{"bibliographic_title":"Angewandte Chemie-International Edition","bibliographic_titleLang":"en"}]}]},"item_10_description_4":{"attribute_name":"\u6284\u9332","attribute_value_mlt":[{"subitem_description":"Aurachins\u2005A and B are alkaloids having 3-hydroxyquinoline N-oxide cores. An efficient method for the synthesis of 3-hydroxyquinoline N-oxides was established and is amenable to the total syntheses of aurachins\u2005A and B. Alkylation of 1-(2-nitrophenyl)butan-2-one with farnesyl bromide took place selectively at the benzylic position, and subsequent treatment of the alkylated product with sodium tert-butoxide in dimethyl sulfoxide gave aurachin\u2005B. Alkylation of 1-(2-nitrophenyl)butan-2-one with an epoxy iodide derived from farnesol was used to access aurachin\u2005A.","subitem_description_language":"en","subitem_description_type":"Abstract"}]},"item_10_identifier_60":{"attribute_name":"URI","attribute_value_mlt":[{"subitem_identifier_type":"DOI","subitem_identifier_uri":"http://doi.org/10.1002/anie.201702204"},{"subitem_identifier_type":"HDL","subitem_identifier_uri":"http://hdl.handle.net/2237/26937"}]},"item_10_publisher_32":{"attribute_name":"\u51fa\u7248\u8005","attribute_value_mlt":[{"subitem_publisher":"Wiley","subitem_publisher_language":"en"}]},"item_10_relation_11":{"attribute_name":"DOI","attribute_value_mlt":[{"subitem_relation_type":"isVersionOf","subitem_relation_type_id":{"subitem_relation_type_id_text":"https://doi.org/10.1002/anie.201702204","subitem_relation_type_select":"DOI"}}]},"item_10_rights_12":{"attribute_name":"\u6a29\u5229","attribute_value_mlt":[{"subitem_rights":"This is the peer reviewed version of the following article: [H. Hattori, S. Yokoshima, T. Fukuyama, Angew. Chem. Int. Ed. 2017, 56, 6980.], which has been published in final form at [http://doi.org/10.1002/anie.201702204]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.","subitem_rights_language":"en"}]},"item_10_select_15":{"attribute_name":"\u8457\u8005\u7248\u30d5\u30e9\u30b0","attribute_value_mlt":[{"subitem_select_item":"author"}]},"item_10_source_id_7":{"attribute_name":"ISSN","attribute_value_mlt":[{"subitem_source_identifier":"1433-7851","subitem_source_identifier_type":"PISSN"}]},"item_1615787544753":{"attribute_name":"\u51fa\u7248\u30bf\u30a4\u30d7","attribute_value_mlt":[{"subitem_version_resource":"http://purl.org/coar/version/c_ab4af688f83e57aa","subitem_version_type":"AM"}]},"item_access_right":{"attribute_name":"\u30a2\u30af\u30bb\u30b9\u6a29","attribute_value_mlt":[{"subitem_access_right":"open access","subitem_access_right_uri":"http://purl.org/coar/access_right/c_abf2"}]},"item_creator":{"attribute_name":"\u8457\u8005","attribute_type":"creator","attribute_value_mlt":[{"creatorNames":[{"creatorName":"Hattori, Haruhiko","creatorNameLang":"en"}],"nameIdentifiers":[{"nameIdentifier":"73363","nameIdentifierScheme":"WEKO"}]},{"creatorNames":[{"creatorName":"Yokoshima, Satoshi","creatorNameLang":"en"}],"nameIdentifiers":[{"nameIdentifier":"73364","nameIdentifierScheme":"WEKO"}]},{"creatorNames":[{"creatorName":"Fukuyama, Tohru","creatorNameLang":"en"}],"nameIdentifiers":[{"nameIdentifier":"73365","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":"2018-06-06"}],"displaytype":"detail","filename":"20170411_hatsutori.pdf","filesize":[{"value":"721.6 kB"}],"format":"application/pdf","licensetype":"license_note","mimetype":"application/pdf","url":{"label":"20170411_hatsutori.pdf \u30d5\u30a1\u30a4\u30eb\u516c\u958b\uff1a2018/06/06","objectType":"fulltext","url":"https://nagoya.repo.nii.ac.jp/record/24722/files/20170411_hatsutori.pdf"},"version_id":"029d3efa-35ba-441e-93ea-aa698df36817"}]},"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":"Total Syntheses of Aurachins A and B","item_titles":{"attribute_name":"\u30bf\u30a4\u30c8\u30eb","attribute_value_mlt":[{"subitem_title":"Total Syntheses of Aurachins A and B","subitem_title_language":"en"}]},"item_type_id":"10","owner":"1","path":["1903/1904/1905"],"pubdate":{"attribute_name":"PubDate","attribute_value":"2017-09-04"},"publish_date":"2017-09-04","publish_status":"0","recid":"24722","relation_version_is_last":true,"title":["Total Syntheses of Aurachins A and B"],"weko_creator_id":"1","weko_shared_id":-1},"updated":"2022-07-08T06:26:32.012609+00:00"}