WEKO3
インデックスリンク
アイテム
{"_buckets": {"deposit": "dc16bd1a-0f19-4430-b075-ca48c667a869"}, "_deposit": {"created_by": 3, "id": "10745", "owners": [3], "pid": {"revision_id": 0, "type": "depid", "value": "10745"}, "status": "published"}, "_oai": {"id": "oai:kanazawa-u.repo.nii.ac.jp:00010745", "sets": ["937"]}, "author_link": ["15050", "16399"], "item_4_biblio_info_8": {"attribute_name": "書誌情報", "attribute_value_mlt": [{"bibliographicIssueDates": {"bibliographicIssueDate": "1977-01-01", "bibliographicIssueDateType": "Issued"}, "bibliographicIssueNumber": "1", "bibliographicPageEnd": "284", "bibliographicPageStart": "280", "bibliographicVolumeNumber": "50", "bibliographic_titles": [{"bibliographic_title": "Bulletin of the Chemical Society of Japan"}]}]}, "item_4_description_21": {"attribute_name": "抄録", "attribute_value_mlt": [{"subitem_description": "The synthesis of a peptide lactone, N-(3-hydroxypicolinyl)-threonyl-D-leucyl-prolylsarcosyl-leucyl-alanyl-alanine Threonine Lactone (21) is described. The t-butoxycarbonyl group of t-butyl O-(t-butoxycarbonyl-alanyl)-N-benzyloxycarbonyl-threonyl-D-leucyl-prolylsarcosinate (12) was deblocked selectively with formic acid in good yield. The coupling of 12 with the azide derived from t-butoxycarbonyl-leucyl-alanine hydrazide (15) with isopentyl nitrite gave a heptapeptide ester 17. Deblocking, cyclization, and hydrogenation gave a heptapeptide lactone 20 which was coupled with 3-hydroxypicolinic acid yielding 21.", "subitem_description_type": "Abstract"}]}, "item_4_publisher_17": {"attribute_name": "出版者", "attribute_value_mlt": [{"subitem_publisher": "The Chemical Society of Japan = 日本化学会"}]}, "item_4_relation_12": {"attribute_name": "DOI", "attribute_value_mlt": [{"subitem_relation_type": "isIdenticalTo", "subitem_relation_type_id": {"subitem_relation_type_id_text": "10.1246/bcsj.50.280", "subitem_relation_type_select": "DOI"}}]}, "item_4_relation_28": {"attribute_name": "関連URI", "attribute_value_mlt": [{"subitem_relation_type_id": {"subitem_relation_type_id_text": "https://www.jstage.jst.go.jp/browse/bcsj", "subitem_relation_type_select": "URI"}}, {"subitem_relation_type_id": {"subitem_relation_type_id_text": "http://www.chemistry.or.jp/", "subitem_relation_type_select": "URI"}}]}, "item_4_rights_23": {"attribute_name": "権利", "attribute_value_mlt": [{"subitem_rights": "Copyright © The Chemical Society of Japan 日本化学会"}]}, "item_4_source_id_11": {"attribute_name": "NCID", "attribute_value_mlt": [{"subitem_source_identifier": "AA00580132", "subitem_source_identifier_type": "NCID"}]}, "item_4_source_id_9": {"attribute_name": "ISSN", "attribute_value_mlt": [{"subitem_source_identifier": "0009-2673", "subitem_source_identifier_type": "ISSN"}]}, "item_4_version_type_25": {"attribute_name": "著者版フラグ", "attribute_value_mlt": [{"subitem_version_resource": "http://purl.org/coar/version/c_970fb48d4fbd8a85", "subitem_version_type": "VoR"}]}, "item_creator": {"attribute_name": "著者", "attribute_type": "creator", "attribute_value_mlt": [{"creatorNames": [{"creatorName": "Kinoshita, Hideki"}], "nameIdentifiers": [{"nameIdentifier": "15050", "nameIdentifierScheme": "WEKO"}, {"nameIdentifier": "20019483", "nameIdentifierScheme": "e-Rad", "nameIdentifierURI": "https://kaken.nii.ac.jp/ja/search/?qm=20019483"}, {"nameIdentifier": "20019483", "nameIdentifierScheme": "研究者番号", "nameIdentifierURI": "https://nrid.nii.ac.jp/nrid/1000020019483"}]}, {"creatorNames": [{"creatorName": "Hiroshi Kotake"}], "nameIdentifiers": [{"nameIdentifier": "16399", "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": "2017-10-03"}], "displaytype": "detail", "download_preview_message": "", "file_order": 0, "filename": "SC-PR-KINOSHITA-H-280.pdf", "filesize": [{"value": "1.0 MB"}], "format": "application/pdf", "future_date_message": "", "is_thumbnail": false, "licensetype": "license_free", "mimetype": "application/pdf", "size": 1000000.0, "url": {"label": "SC-PR-KINOSHITA-H-280.pdf", "url": "https://kanazawa-u.repo.nii.ac.jp/record/10745/files/SC-PR-KINOSHITA-H-280.pdf"}, "version_id": "e1d267fb-c52a-4f12-8916-e0fe7e2c103c"}]}, "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": "Synthesis of a peptide lactone, N (3 hydroxypicolinyl) threonyl D leucyl prolylsarcosyl leucyl alanyl alanine threonine lactone", "item_titles": {"attribute_name": "タイトル", "attribute_value_mlt": [{"subitem_title": "Synthesis of a peptide lactone, N (3 hydroxypicolinyl) threonyl D leucyl prolylsarcosyl leucyl alanyl alanine threonine lactone"}]}, "item_type_id": "4", "owner": "3", "path": ["937"], "permalink_uri": "http://hdl.handle.net/2297/38256", "pubdate": {"attribute_name": "公開日", "attribute_value": "2017-10-03"}, "publish_date": "2017-10-03", "publish_status": "0", "recid": "10745", "relation": {}, "relation_version_is_last": true, "title": ["Synthesis of a peptide lactone, N (3 hydroxypicolinyl) threonyl D leucyl prolylsarcosyl leucyl alanyl alanine threonine lactone"], "weko_shared_id": -1}
Synthesis of a peptide lactone, N (3 hydroxypicolinyl) threonyl D leucyl prolylsarcosyl leucyl alanyl alanine threonine lactone
http://hdl.handle.net/2297/38256
http://hdl.handle.net/2297/38256fa1e33fc-f118-42e6-acf1-e88489e5ddb6
名前 / ファイル | ライセンス | アクション |
---|---|---|
SC-PR-KINOSHITA-H-280.pdf (1.0 MB)
|
|
Item type | 学術雑誌論文 / Journal Article(1) | |||||
---|---|---|---|---|---|---|
公開日 | 2017-10-03 | |||||
タイトル | ||||||
タイトル | Synthesis of a peptide lactone, N (3 hydroxypicolinyl) threonyl D leucyl prolylsarcosyl leucyl alanyl alanine threonine lactone | |||||
言語 | ||||||
言語 | eng | |||||
資源タイプ | ||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
資源タイプ | journal article | |||||
著者 |
Kinoshita, Hideki
× Kinoshita, Hideki× Hiroshi Kotake |
|||||
書誌情報 |
Bulletin of the Chemical Society of Japan 巻 50, 号 1, p. 280-284, 発行日 1977-01-01 |
|||||
ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 0009-2673 | |||||
NCID | ||||||
収録物識別子タイプ | NCID | |||||
収録物識別子 | AA00580132 | |||||
DOI | ||||||
関連タイプ | isIdenticalTo | |||||
識別子タイプ | DOI | |||||
関連識別子 | 10.1246/bcsj.50.280 | |||||
出版者 | ||||||
出版者 | The Chemical Society of Japan = 日本化学会 | |||||
抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | The synthesis of a peptide lactone, N-(3-hydroxypicolinyl)-threonyl-D-leucyl-prolylsarcosyl-leucyl-alanyl-alanine Threonine Lactone (21) is described. The t-butoxycarbonyl group of t-butyl O-(t-butoxycarbonyl-alanyl)-N-benzyloxycarbonyl-threonyl-D-leucyl-prolylsarcosinate (12) was deblocked selectively with formic acid in good yield. The coupling of 12 with the azide derived from t-butoxycarbonyl-leucyl-alanine hydrazide (15) with isopentyl nitrite gave a heptapeptide ester 17. Deblocking, cyclization, and hydrogenation gave a heptapeptide lactone 20 which was coupled with 3-hydroxypicolinic acid yielding 21. | |||||
権利 | ||||||
権利情報 | Copyright © The Chemical Society of Japan 日本化学会 | |||||
著者版フラグ | ||||||
出版タイプ | VoR | |||||
出版タイプResource | http://purl.org/coar/version/c_970fb48d4fbd8a85 | |||||
関連URI | ||||||
識別子タイプ | URI | |||||
関連識別子 | https://www.jstage.jst.go.jp/browse/bcsj | |||||
関連URI | ||||||
識別子タイプ | URI | |||||
関連識別子 | http://www.chemistry.or.jp/ |