{"created":"2025-02-21T03:36:56.250456+00:00","id":2006954,"links":{},"metadata":{"_buckets":{"deposit":"18cc19d1-5d05-45c9-9d06-52e409319a2f"},"_deposit":{"created_by":41,"id":"2006954","owners":[41],"pid":{"revision_id":0,"type":"depid","value":"2006954"},"status":"published"},"_oai":{"id":"oai:hiroshima.repo.nii.ac.jp:02006954","sets":["1730444907710"]},"author_link":[],"item_1617186331708":{"attribute_name":"Title","attribute_value_mlt":[{"subitem_title":"CHEMISTRY OF ANTI-HIV ACTIVE TRIMERIC PYRANONAPHTHO-QUINONE CONOCURVONE: SYNTHETIC STUDIES TOWARDS MONOMERIC TERETIFOLIONE B AND RELATED COMPOUNDS","subitem_title_language":"en"}]},"item_1617186419668":{"attribute_name":"Creator","attribute_type":"creator","attribute_value_mlt":[{"creatorNames":[{"creatorName":"Kumamoto, Takuya","creatorNameLang":"en"}],"familyNames":[{"familyName":"Kumamoto","familyNameLang":"en"}],"givenNames":[{"givenName":"Takuya","givenNameLang":"en"}]},{"creatorNames":[{"creatorName":"Katakawa, Kazuaki","creatorNameLang":"en"}],"familyNames":[{"familyName":"Katakawa","familyNameLang":"en"}],"givenNames":[{"givenName":"Kazuaki","givenNameLang":"en"}]}]},"item_1617186476635":{"attribute_name":"Access Rights","attribute_value_mlt":[{"subitem_access_right":"open access","subitem_access_right_uri":"http://purl.org/coar/access_right/c_abf2"}]},"item_1617186499011":{"attribute_name":"Rights","attribute_value_mlt":[{"subitem_rights":"Copyright (c) 2019 The Japan Institute of Heterocyclic Chemistry"},{"subitem_rights":"This is the uncorrected proof, and is not the published version. Please cite only the published version. この論文は著者校正前原稿であり、出版社版ではありません。引用の際には出版社版をご確認、ご利用ください。"}]},"item_1617186626617":{"attribute_name":"Description","attribute_value_mlt":[{"subitem_description":"Pyranonaphthoquinone natural products are widely distributed in plants and microorganisms and have diverse biological activities. Angular benzochromenes are a small class of natural products isolated from Conospermum and Pentas plants. Of these, conocurvone was isolated from Conospermum as a trimeric pyranonaphthoquinone that has potent anti-HIV activity. We have focused on the total synthesis of compounds that exhibit biological activity or whose activity is enhanced upon oligomerization. This review describes the discovery and biological activities of the trimeric pyranonaphthoquinone conocurvone and related compounds, as well as our and other researchers’ synthetic studies toward monomeric pyranonaphthoquinones.","subitem_description_language":"en"},{"subitem_description":"This work was partially supported by The Uehara Memorial Foundation, a Grant from Musashino Joshi-Gakuin, and JSPS KAKENHI Grant Number JP19K06975.","subitem_description_type":"Other"}]},"item_1617186643794":{"attribute_name":"Publisher","attribute_value_mlt":[{"subitem_publisher":"The Japan Institute of Heterocyclic Chemistry"}]},"item_1617186702042":{"attribute_name":"Language","attribute_value_mlt":[{"subitem_language":"eng"}]},"item_1617186920753":{"attribute_name":"Source Identifier","attribute_value_mlt":[{"subitem_source_identifier":"1881-0942","subitem_source_identifier_type":"ISSN"}]},"item_1617187024783":{"attribute_name":"Page Start","attribute_value_mlt":[{"subitem_start_page":"177"}]},"item_1617187056579":{"attribute_name":"Bibliographic Information","attribute_value_mlt":[{"bibliographicIssueDates":{"bibliographicIssueDate":"2019-12-23","bibliographicIssueDateType":"Issued"},"bibliographicIssueNumber":"2","bibliographicPageEnd":"193","bibliographicPageStart":"177","bibliographicVolumeNumber":"100","bibliographic_titles":[{"bibliographic_title":"Heterocycles"},{"bibliographic_title":"Heterocycles"}]}]},"item_1617258105262":{"attribute_name":"Resource Type","attribute_value_mlt":[{"resourcetype":"journal article","resourceuri":"http://purl.org/coar/resource_type/c_6501"}]},"item_1617265215918":{"attribute_name":"Version Type","attribute_value_mlt":[{"subitem_version_resource":"http://purl.org/coar/version/c_970fb48d4fbd8a85","subitem_version_type":"VoR"}]},"item_1617353299429":{"attribute_name":"Relation","attribute_value_mlt":[{"subitem_relation_type_id":{"subitem_relation_type_id_text":"10.3987/REV-19-915","subitem_relation_type_select":"DOI"}},{"subitem_relation_type_id":{"subitem_relation_type_id_text":"https://doi.org/10.3987/REV-19-915","subitem_relation_type_select":"DOI"}}]},"item_1617605131499":{"attribute_name":"File","attribute_type":"file","attribute_value_mlt":[{"accessrole":"open_access","date":[{"dateType":"Available","dateValue":"2023-03-18"}],"displaytype":"simple","filename":"Heterocycles_100_177.pdf","filesize":[{"value":"721.0 KB"}],"mimetype":"application/pdf","url":{"objectType":"fulltext","url":"https://hiroshima.repo.nii.ac.jp/record/2006954/files/Heterocycles_100_177.pdf"},"version_id":"9bb267e6-b9da-401a-a939-0ae72a90f0df"}]},"item_1732771732025":{"attribute_name":"旧ID","attribute_value":"49148"},"item_title":"CHEMISTRY OF ANTI-HIV ACTIVE TRIMERIC PYRANONAPHTHO-QUINONE CONOCURVONE: SYNTHETIC STUDIES TOWARDS MONOMERIC TERETIFOLIONE B AND RELATED COMPOUNDS","item_type_id":"40003","owner":"41","path":["1730444907710"],"pubdate":{"attribute_name":"PubDate","attribute_value":"2023-03-18"},"publish_date":"2023-03-18","publish_status":"0","recid":"2006954","relation_version_is_last":true,"title":["CHEMISTRY OF ANTI-HIV ACTIVE TRIMERIC PYRANONAPHTHO-QUINONE CONOCURVONE: SYNTHETIC STUDIES TOWARDS MONOMERIC TERETIFOLIONE B AND RELATED COMPOUNDS"],"weko_creator_id":"41","weko_shared_id":-1},"updated":"2025-02-21T08:50:56.676361+00:00"}