WEKO3
AND
アイテム
{"_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"}, "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"}]}]}, "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_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"}]}, "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.\""}]}, "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": "ISSN"}]}, "item_creator": {"attribute_name": "\u8457\u8005", "attribute_type": "creator", "attribute_value_mlt": [{"creatorNames": [{"creatorName": "Hattori, Haruhiko"}], "nameIdentifiers": [{"nameIdentifier": "73363", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Yokoshima, Satoshi"}], "nameIdentifiers": [{"nameIdentifier": "73364", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Fukuyama, Tohru"}], "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", "download_preview_message": "", "file_order": 0, "filename": "20170411_hatsutori.pdf", "filesize": [{"value": "721.6 kB"}], "format": "application/pdf", "future_date_message": "", "is_thumbnail": false, "licensetype": "license_free", "mimetype": "application/pdf", "size": 721600.0, "url": {"label": "20170411_hatsutori.pdf \u30d5\u30a1\u30a4\u30eb\u516c\u958b\uff1a2018/06/06", "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"}]}, "item_type_id": "10", "owner": "1", "path": ["1903/1904/1905"], "permalink_uri": "http://hdl.handle.net/2237/26937", "pubdate": {"attribute_name": "\u516c\u958b\u65e5", "attribute_value": "2017-09-04"}, "publish_date": "2017-09-04", "publish_status": "0", "recid": "24722", "relation": {}, "relation_version_is_last": true, "title": ["Total Syntheses of Aurachins A and B"], "weko_shared_id": null}
Total Syntheses of Aurachins A and B
http://hdl.handle.net/2237/26937
cc34fe8a-3331-4499-8eda-4ee92af0a262
名前 / ファイル | ライセンス | アクション | |
---|---|---|---|
![]() |
|
Item type | 学術雑誌論文 / Journal Article(1) | |||||
---|---|---|---|---|---|---|
公開日 | 2017-09-04 | |||||
タイトル | ||||||
タイトル | Total Syntheses of Aurachins A and B | |||||
著者 |
Hattori, Haruhiko
× Hattori, Haruhiko× Yokoshima, Satoshi× Fukuyama, Tohru |
|||||
権利 | ||||||
権利情報 | "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." | |||||
抄録 | ||||||
内容記述 | Aurachins A 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 A 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 B. Alkylation of 1-(2-nitrophenyl)butan-2-one with an epoxy iodide derived from farnesol was used to access aurachin A. | |||||
内容記述タイプ | Abstract | |||||
出版者 | ||||||
出版者 | Wiley | |||||
言語 | ||||||
言語 | eng | |||||
資源タイプ | ||||||
資源タイプresource | http://purl.org/coar/resource_type/c_6501 | |||||
タイプ | journal article | |||||
ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 1433-7851 | |||||
書誌情報 |
Angewandte Chemie-International Edition 巻 56, 号 24, p. 6980-6983, 発行日 2017-06-06 |
|||||
著者版フラグ | ||||||
値 | author | |||||
URI | ||||||
識別子 | http://doi.org/10.1002/anie.201702204 | |||||
識別子タイプ | DOI | |||||
URI | ||||||
識別子 | http://hdl.handle.net/2237/26937 | |||||
識別子タイプ | HDL |