WEKO3
アイテム
{"_buckets": {"deposit": "feecde46-12d0-4849-8e3f-3848be34349f"}, "_deposit": {"created_by": 1, "id": "2953", "owners": [1], "pid": {"revision_id": 0, "type": "depid", "value": "2953"}, "status": "published"}, "_oai": {"id": "oai:kanagawa-u.repo.nii.ac.jp:00002953", "sets": ["239"]}, "author_link": ["5989", "5994", "5991", "5993", "5990", "5992"], "item_7_biblio_info_7": {"attribute_name": "書誌情報", "attribute_value_mlt": [{"bibliographicIssueDates": {"bibliographicIssueDate": "1993", "bibliographicIssueDateType": "Issued"}, "bibliographicIssueNumber": "4", "bibliographicPageEnd": "1165", "bibliographicPageStart": "1156", "bibliographicVolumeNumber": "66", "bibliographic_titles": [{"bibliographic_title": "Bulletin of the Chemical Society of Japan"}]}]}, "item_7_description_4": {"attribute_name": "抄録", "attribute_value_mlt": [{"subitem_description": "Various kinds of nonbranched and methyl-branched 6-deoxyhex-5-enopyranoside derivatives were prepared from 6-bromo-6-deoxy or 6-O-p-tolylsulfonylhexopyranoside in a one-pot procedure by a successive treatment with iodide anion and 1,8-diazabicyclo[5.4.0]undec-7-ene in dimethyl sulfoxide. The scope and limitations of this reaction have become apparent by observing the reactions of 18 substrates. The yields of altropyranoside and 2-deoxyribo-hexopyranoside derivatives were high, except for the 2,3-anhydropyranoside derivative. Methyl-branched 6-deoxyhex-5-enopyranoside derivatives were also obtained in practical yields.", "subitem_description_type": "Abstract"}]}, "item_7_description_40": {"attribute_name": "資源タイプ", "attribute_value_mlt": [{"subitem_description": "Article", "subitem_description_type": "Other"}]}, "item_7_publisher_33": {"attribute_name": "出版者", "attribute_value_mlt": [{"subitem_publisher": "日本化学会"}]}, "item_7_relation_12": {"attribute_name": "DOI", "attribute_value_mlt": [{"subitem_relation_type": "isIdenticalTo", "subitem_relation_type_id": {"subitem_relation_type_id_text": "10.1246/bcsj.66.1156", "subitem_relation_type_select": "DOI"}}]}, "item_7_source_id_10": {"attribute_name": "書誌レコードID", "attribute_value_mlt": [{"subitem_source_identifier": "AA00580132", "subitem_source_identifier_type": "NCID"}]}, "item_7_source_id_8": {"attribute_name": "ISSN", "attribute_value_mlt": [{"subitem_source_identifier": "0009-2673", "subitem_source_identifier_type": "ISSN"}]}, "item_7_version_type_16": {"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": "佐藤, 憲一"}], "nameIdentifiers": [{"nameIdentifier": "5989", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Sato, Ken-ichi"}], "nameIdentifiers": [{"nameIdentifier": "5990", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Kubo, Noriyuki"}], "nameIdentifiers": [{"nameIdentifier": "5991", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Takada, Ritsuko"}], "nameIdentifiers": [{"nameIdentifier": "5992", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "佐久間, 詔悟"}], "nameIdentifiers": [{"nameIdentifier": "5993", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Sakuma, Shogo"}], "nameIdentifiers": [{"nameIdentifier": "5994", "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": "2018-11-16"}], "displaytype": "detail", "download_preview_message": "", "file_order": 0, "filename": "佐藤・化学-019.pdf", "filesize": [{"value": "7.5 MB"}], "format": "application/pdf", "future_date_message": "", "is_thumbnail": false, "licensetype": "license_free", "mimetype": "application/pdf", "size": 7500000.0, "url": {"label": "佐藤・化学-019.pdf", "url": "https://kanagawa-u.repo.nii.ac.jp/record/2953/files/佐藤・化学-019.pdf"}, "version_id": "ec179e80-3b28-4630-8b06-5904d4a2b2be"}]}, "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": "Syntheses of 6-Deoxyhex-5-enopyranosides from 6-Bromo-6-deoxy- or 6-O-p-Tolylsulfonylhexopyranosides by the Use of DBU in DMSO", "item_titles": {"attribute_name": "タイトル", "attribute_value_mlt": [{"subitem_title": "Syntheses of 6-Deoxyhex-5-enopyranosides from 6-Bromo-6-deoxy- or 6-O-p-Tolylsulfonylhexopyranosides by the Use of DBU in DMSO"}]}, "item_type_id": "7", "owner": "1", "path": ["239"], "permalink_uri": "http://hdl.handle.net/10487/8180", "pubdate": {"attribute_name": "公開日", "attribute_value": "2011-01-28"}, "publish_date": "2011-01-28", "publish_status": "0", "recid": "2953", "relation": {}, "relation_version_is_last": true, "title": ["Syntheses of 6-Deoxyhex-5-enopyranosides from 6-Bromo-6-deoxy- or 6-O-p-Tolylsulfonylhexopyranosides by the Use of DBU in DMSO"], "weko_shared_id": -1}
Syntheses of 6-Deoxyhex-5-enopyranosides from 6-Bromo-6-deoxy- or 6-O-p-Tolylsulfonylhexopyranosides by the Use of DBU in DMSO
http://hdl.handle.net/10487/8180
http://hdl.handle.net/10487/8180f378391c-82fe-4d04-8785-687e9ae06618
名前 / ファイル | ライセンス | アクション |
---|---|---|
佐藤・化学-019.pdf (7.5 MB)
|
|
Item type | 学術雑誌論文 / Journal Article(1) | |||||
---|---|---|---|---|---|---|
公開日 | 2011-01-28 | |||||
タイトル | ||||||
タイトル | Syntheses of 6-Deoxyhex-5-enopyranosides from 6-Bromo-6-deoxy- or 6-O-p-Tolylsulfonylhexopyranosides by the Use of DBU in DMSO | |||||
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 |
佐藤, 憲一
× 佐藤, 憲一× Sato, Ken-ichi× Kubo, Noriyuki× Takada, Ritsuko× 佐久間, 詔悟× Sakuma, Shogo |
|||||
抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | Various kinds of nonbranched and methyl-branched 6-deoxyhex-5-enopyranoside derivatives were prepared from 6-bromo-6-deoxy or 6-O-p-tolylsulfonylhexopyranoside in a one-pot procedure by a successive treatment with iodide anion and 1,8-diazabicyclo[5.4.0]undec-7-ene in dimethyl sulfoxide. The scope and limitations of this reaction have become apparent by observing the reactions of 18 substrates. The yields of altropyranoside and 2-deoxyribo-hexopyranoside derivatives were high, except for the 2,3-anhydropyranoside derivative. Methyl-branched 6-deoxyhex-5-enopyranoside derivatives were also obtained in practical yields. | |||||
書誌情報 |
Bulletin of the Chemical Society of Japan 巻 66, 号 4, p. 1156-1165, 発行日 1993 |
|||||
ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 0009-2673 | |||||
書誌レコードID | ||||||
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.66.1156 | |||||
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 | |||||
出版者 | ||||||
出版者 | 日本化学会 | |||||
資源タイプ | ||||||
内容記述タイプ | Other | |||||
内容記述 | Article |