WEKO3
アイテム
{"_buckets": {"deposit": "121b42a6-001f-4afc-ba7f-a34c65e55983"}, "_deposit": {"id": "54853", "owners": [], "pid": {"revision_id": 0, "type": "depid", "value": "54853"}, "status": "published"}, "_oai": {"id": "oai:tsukuba.repo.nii.ac.jp:00054853", "sets": ["487", "2589", "7996"]}, "item_5_biblio_info_6": {"attribute_name": "書誌情報", "attribute_value_mlt": [{"bibliographicIssueDates": {"bibliographicIssueDate": "2020-03", "bibliographicIssueDateType": "Issued"}, "bibliographicIssueNumber": "3", "bibliographicPageEnd": "266", "bibliographicPageStart": "264", "bibliographicVolumeNumber": "49", "bibliographic_titles": [{}, {"bibliographic_title": "Chemistry Letters", "bibliographic_titleLang": "en"}]}]}, "item_5_description_4": {"attribute_name": "抄録", "attribute_value_mlt": [{"subitem_description": "The [4 + 2] cycloaddition of styrenes with arynes was achieved via 1:1 cross-coupling by a nickel catalyst. This protocol applies to a variety of styrenes and arynes generated in situ from o-(trimethylsilyl)aryl triflates to afford 9,10-dihydrophenanthrenes involving substituted aromatic rings. By using this method, a naturally occurring stilbenoid is easily synthesized.", "subitem_description_type": "Abstract"}]}, "item_5_publisher_27": {"attribute_name": "出版者", "attribute_value_mlt": [{"subitem_publisher": "Chemical Society of Japan"}]}, "item_5_publisher_28": {"attribute_name": "出版者別名", "attribute_value_mlt": [{"subitem_publisher": "日本化学会"}]}, "item_5_relation_11": {"attribute_name": "DOI", "attribute_value_mlt": [{"subitem_relation_type_id": {"subitem_relation_type_id_text": "10.1246/cl.190906", "subitem_relation_type_select": "DOI"}}]}, "item_5_rights_12": {"attribute_name": "権利", "attribute_value_mlt": [{"subitem_rights": "© 2020 The Chemical Society of Japan"}]}, "item_5_select_15": {"attribute_name": "著者版フラグ", "attribute_value_mlt": [{"subitem_select_item": "author"}]}, "item_5_source_id_7": {"attribute_name": "ISSN", "attribute_value_mlt": [{"subitem_source_identifier": "0366-7022", "subitem_source_identifier_type": "ISSN"}]}, "item_5_source_id_9": {"attribute_name": "書誌レコードID", "attribute_value_mlt": [{"subitem_source_identifier": "AA00603318", "subitem_source_identifier_type": "NCID"}]}, "item_creator": {"attribute_name": "著者", "attribute_type": "creator", "attribute_value_mlt": [{"creatorNames": [{"creatorName": "藤田, 健志"}, {"creatorName": "フジタ, タケシ", "creatorNameLang": "ja-Kana"}, {"creatorName": "FUJITA, Takeshi", "creatorNameLang": "en"}], "nameIdentifiers": [{"nameIdentifier": "204764", "nameIdentifierScheme": "WEKO"}, {"nameIdentifier": "60603066", "nameIdentifierScheme": "e-Rad", "nameIdentifierURI": "https://nrid.nii.ac.jp/ja/nrid/1000060603066"}, {"nameIdentifier": "0000000665", "nameIdentifierScheme": "筑波大学研究者総覧", "nameIdentifierURI": "http://trios.tsukuba.ac.jp/researcher/0000000665"}]}, {"creatorNames": [{"creatorName": "市川, 淳士"}, {"creatorName": "イチカワ, ジュンジ", "creatorNameLang": "ja-Kana"}, {"creatorName": "ICHIKAWA, Junji", "creatorNameLang": "en"}], "nameIdentifiers": [{"nameIdentifier": "148", "nameIdentifierScheme": "WEKO"}, {"nameIdentifier": "70184611", "nameIdentifierScheme": "e-Rad", "nameIdentifierURI": "https://nrid.nii.ac.jp/ja/nrid/1000070184611"}, {"nameIdentifier": "0000000655", "nameIdentifierScheme": "筑波大学研究者総覧", "nameIdentifierURI": "http://trios.tsukuba.ac.jp/researcher/0000000655"}]}, {"creatorNames": [{"creatorName": "Kubo, Teruhiko", "creatorNameLang": "en"}], "nameIdentifiers": [{"nameIdentifier": "220260", "nameIdentifierScheme": "WEKO"}]}]}, "item_files": {"attribute_name": "ファイル情報", "attribute_type": "file", "attribute_value_mlt": [{"accessrole": "open_date", "date": [{"dateType": "Available", "dateValue": "2020-06-30"}], "displaytype": "detail", "download_preview_message": "", "file_order": 0, "filename": "CL_49-3.pdf", "filesize": [{"value": "543.8 kB"}], "format": "application/pdf", "future_date_message": "", "is_thumbnail": false, "licensetype": "license_free", "mimetype": "application/pdf", "size": 543800.0, "url": {"label": "CL_49-3", "url": "https://tsukuba.repo.nii.ac.jp/record/54853/files/CL_49-3.pdf"}, "version_id": "9e39297f-1031-48dd-bce8-5bdc107541a5"}]}, "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": "Nickel-catalyzed [4 + 2] Cycloaddition of Styrenes with Arynes via 1:1 Cross-coupling : Synthesis of 9,10-Dihydrophenanthrenes", "item_titles": {"attribute_name": "タイトル", "attribute_value_mlt": [{"subitem_title": "Nickel-catalyzed [4 + 2] Cycloaddition of Styrenes with Arynes via 1:1 Cross-coupling : Synthesis of 9,10-Dihydrophenanthrenes", "subitem_title_language": "en"}]}, "item_type_id": "5", "owner": "1", "path": ["487", "2589", "7996"], "permalink_uri": "http://hdl.handle.net/2241/00160261", "pubdate": {"attribute_name": "公開日", "attribute_value": "2020-06-30"}, "publish_date": "2020-06-30", "publish_status": "0", "recid": "54853", "relation": {}, "relation_version_is_last": true, "title": ["Nickel-catalyzed [4 + 2] Cycloaddition of Styrenes with Arynes via 1:1 Cross-coupling : Synthesis of 9,10-Dihydrophenanthrenes"], "weko_shared_id": 5}
Nickel-catalyzed [4 + 2] Cycloaddition of Styrenes with Arynes via 1:1 Cross-coupling : Synthesis of 9,10-Dihydrophenanthrenes
http://hdl.handle.net/2241/00160261
http://hdl.handle.net/2241/001602612deb64c5-cc43-4525-b893-9006aca34d86
名前 / ファイル | ライセンス | アクション |
---|---|---|
CL_49-3 (543.8 kB)
|
|
Item type | Journal Article(1) | |||||
---|---|---|---|---|---|---|
公開日 | 2020-06-30 | |||||
タイトル | ||||||
言語 | en | |||||
タイトル | Nickel-catalyzed [4 + 2] Cycloaddition of Styrenes with Arynes via 1:1 Cross-coupling : Synthesis of 9,10-Dihydrophenanthrenes | |||||
言語 | ||||||
言語 | eng | |||||
資源タイプ | ||||||
資源 | http://purl.org/coar/resource_type/c_6501 | |||||
タイプ | journal article | |||||
著者 |
藤田, 健志
× 藤田, 健志× 市川, 淳士× Kubo, Teruhiko |
|||||
抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | The [4 + 2] cycloaddition of styrenes with arynes was achieved via 1:1 cross-coupling by a nickel catalyst. This protocol applies to a variety of styrenes and arynes generated in situ from o-(trimethylsilyl)aryl triflates to afford 9,10-dihydrophenanthrenes involving substituted aromatic rings. By using this method, a naturally occurring stilbenoid is easily synthesized. | |||||
書誌情報 |
en : Chemistry Letters 巻 49, 号 3, p. 264-266, 発行日 2020-03 |
|||||
ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 0366-7022 | |||||
書誌レコードID | ||||||
収録物識別子タイプ | NCID | |||||
収録物識別子 | AA00603318 | |||||
DOI | ||||||
識別子タイプ | DOI | |||||
関連識別子 | 10.1246/cl.190906 | |||||
権利 | ||||||
権利情報 | © 2020 The Chemical Society of Japan | |||||
著者版フラグ | ||||||
値 | author | |||||
出版者 | ||||||
出版者 | Chemical Society of Japan | |||||
出版者別名 | ||||||
出版者 | 日本化学会 |