{"created":"2021-09-08T02:58:14.091440+00:00","id":2001390,"links":{},"metadata":{"_buckets":{"deposit":"39edf5e2-d253-4822-852f-2986c8592209"},"_deposit":{"created_by":17,"id":"2001390","owner":"17","owners":[17],"owners_ext":{"displayname":"図書情報係","username":"repository"},"pid":{"revision_id":0,"type":"depid","value":"2001390"},"status":"published"},"_oai":{"id":"oai:nagoya.repo.nii.ac.jp:02001390","sets":["320:321:322"]},"author_link":[],"control_number":"2001390","item_1615768549627":{"attribute_name":"出版タイプ","attribute_value_mlt":[{"subitem_version_resource":"http://purl.org/coar/version/c_ab4af688f83e57aa","subitem_version_type":"AM"}]},"item_1629683748249":{"attribute_name":"日付","attribute_value_mlt":[{"subitem_date_issued_datetime":"2022-01-01","subitem_date_issued_type":"Available"}]},"item_9_biblio_info_6":{"attribute_name":"書誌情報","attribute_value_mlt":[{"bibliographicIssueDates":{"bibliographicIssueDate":"2021-01","bibliographicIssueDateType":"Issued"},"bibliographicIssueNumber":"1","bibliographicPageEnd":"169","bibliographicPageStart":"164","bibliographicVolumeNumber":"10","bibliographic_titles":[{"bibliographic_title":"Asian Journal of Organic Chemistry","bibliographic_titleLang":"en"}]}]},"item_9_description_4":{"attribute_name":"内容記述","attribute_value_mlt":[{"subitem_description":"We report a chemoselective tandem oxidative cyclization/aromatization of indole derivatives tethered to aniline sulfonamides using catalytic amount of tetrabutylammonium iodide in the presence of tert-butyl hydroperoxide (TBHP) as an oxidant under nearly neutral conditions at room temperature. The corresponding indolo[2,3-b]quinolines were obtained as sulfonate salts, which could be easily isolated in analytically pure form via only a simple filtration of the crude reaction mixture. The natural product quinindoline could be easily obtained after basic work-up of the sulfonate salt. Control experiments revealed that both ionic and radical active species could be generated in situ under mild conditions for the corresponding oxidative transformations to proceed in a chemoselective manner.","subitem_description_language":"en","subitem_description_type":"Abstract"}]},"item_9_publisher_32":{"attribute_name":"出版者","attribute_value_mlt":[{"subitem_publisher":"Wiley","subitem_publisher_language":"en"}]},"item_9_relation_43":{"attribute_name":"関連情報","attribute_value_mlt":[{"subitem_relation_type":"isVersionOf","subitem_relation_type_id":{"subitem_relation_type_id_text":"https://doi.org/10.1002/ajoc.202000570","subitem_relation_type_select":"DOI"}}]},"item_9_rights_12":{"attribute_name":"権利","attribute_value_mlt":[{"subitem_rights":"\"This is the peer reviewed version of the following article: [M. Uyanik, H. Tanaka, K. Ishihara, Asian J. Org. Chem. 2021, 10, 164.], which has been published in final form at [https://doi.org/10.1002/ajoc.202000570]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited.\"","subitem_rights_language":"en"}]},"item_9_source_id_7":{"attribute_name":"収録物識別子","attribute_value_mlt":[{"subitem_source_identifier":"2193-5815","subitem_source_identifier_type":"EISSN"}]},"item_access_right":{"attribute_name":"アクセス権","attribute_value_mlt":[{"subitem_access_right":"open access","subitem_access_right_uri":"http://purl.org/coar/access_right/c_abf2"}]},"item_creator":{"attribute_name":"著者","attribute_type":"creator","attribute_value_mlt":[{"creatorNames":[{"creatorName":"Uyanik, Muhammet","creatorNameLang":"en"}]},{"creatorNames":[{"creatorName":"Tanaka, Hiroki","creatorNameLang":"en"}]},{"creatorNames":[{"creatorName":"Ishihara, Kazuaki","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":"2022-01-01"}],"displaytype":"detail","filename":"Uyanik.pdf","filesize":[{"value":"1.8 MB"}],"format":"application/pdf","mimetype":"application/pdf","url":{"objectType":"fulltext","url":"https://nagoya.repo.nii.ac.jp/record/2001390/files/Uyanik.pdf"},"version_id":"8d97c630-cc17-4fa0-8de5-02a1bf32310b"}]},"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":"I^+/TBHP Catalysis For Tandem Oxidative Cyclization To Indolo[2,3-b]quinolines","item_titles":{"attribute_name":"タイトル","attribute_value_mlt":[{"subitem_title":"I^+/TBHP Catalysis For Tandem Oxidative Cyclization To Indolo[2,3-b]quinolines","subitem_title_language":"en"}]},"item_type_id":"40001","owner":"17","path":["322"],"pubdate":{"attribute_name":"PubDate","attribute_value":"2021-09-08"},"publish_date":"2021-09-08","publish_status":"0","recid":"2001390","relation_version_is_last":true,"title":["I^+/TBHP Catalysis For Tandem Oxidative Cyclization To Indolo[2,3-b]quinolines"],"weko_creator_id":"17","weko_shared_id":-1},"updated":"2023-01-16T05:13:27.861483+00:00"}