{"_buckets": {"deposit": "4f0b409d-6316-48d1-bc53-a0e112a8aa4c"}, "_deposit": {"id": "11826", "owners": [], "pid": {"revision_id": 0, "type": "depid", "value": "11826"}, "status": "published"}, "_oai": {"id": "oai:soar-ir.repo.nii.ac.jp:00011826"}, "item_6_biblio_info_6": {"attribute_name": "\u66f8\u8a8c\u60c5\u5831", "attribute_value_mlt": [{"bibliographicIssueDates": {"bibliographicIssueDate": "2012-03-21", "bibliographicIssueDateType": "Issued"}, "bibliographicIssueNumber": "12", "bibliographicPageEnd": "1496", "bibliographicPageStart": "1493", "bibliographicVolumeNumber": "53", "bibliographic_titles": [{"bibliographic_title": "TETRAHEDRON LETTERS"}]}]}, "item_6_description_20": {"attribute_name": "\u6284\u9332", "attribute_value_mlt": [{"subitem_description": "Azulene derivatives reacted with 2-indolinones in the presence of triflic anhydride (Tf2O) to afford 1-(indo1-2-yl)azulenes in good yields. In the cases of the reaction of 6-tert-butyl-1-(methylthio)azulene (11) and 1-(1,4-dihydropyridin-4-yl)azulene 14, 1,1\u0027-biazulene derivative 24 and 1-(indo1-2-yl)azulene (2) were obtained under the similar reaction conditions, respectively, instead of the presumed electrophilic substitution products.", "subitem_description_type": "Abstract"}]}, "item_6_description_30": {"attribute_name": "\u8cc7\u6e90\u30bf\u30a4\u30d7\uff08\u30b3\u30f3\u30c6\u30f3\u30c4\u306e\u7a2e\u985e\uff09", "attribute_value_mlt": [{"subitem_description": "Article", "subitem_description_type": "Other"}]}, "item_6_description_5": {"attribute_name": "\u5f15\u7528", "attribute_value_mlt": [{"subitem_description": "TETRAHEDRON LETTERS. 53(12):1493-1496 (2012)", "subitem_description_type": "Other"}]}, "item_6_link_3": {"attribute_name": "\u4fe1\u5dde\u5927\u5b66\u7814\u7a76\u8005\u7dcf\u89a7\u3078\u306e\u30ea\u30f3\u30af", "attribute_value_mlt": [{"subitem_link_text": "Shoji, Taku", "subitem_link_url": "http://soar-rd.shinshu-u.ac.jp/profile/ja.gmShOakh.html"}]}, "item_6_link_67": {"attribute_name": "WoS", "attribute_value_mlt": [{"subitem_link_text": "Web of Science", "subitem_link_url": "http://gateway.isiknowledge.com/gateway/Gateway.cgi?\u0026GWVersion=2\u0026SrcAuth=ShinshuUniv\u0026SrcApp=ShinshuUniv\u0026DestLinkType=FullRecord\u0026DestApp=WOS\u0026KeyUT=000301563300016"}]}, "item_6_publisher_4": {"attribute_name": "\u51fa\u7248\u8005", "attribute_value_mlt": [{"subitem_publisher": "PERGAMON-ELSEVIER SCIENCE LTD"}]}, "item_6_relation_48": {"attribute_name": "DOI", "attribute_value_mlt": [{"subitem_relation_name": [{"subitem_relation_name_text": "10.1016/j.tetlet.2012.01.044"}], "subitem_relation_type_id": {"subitem_relation_type_id_text": "http://dx.doi.org/10.1016/j.tetlet.2012.01.044", "subitem_relation_type_select": "DOI"}}]}, "item_6_select_64": {"attribute_name": "\u8457\u8005\u7248\u30d5\u30e9\u30b0", "attribute_value_mlt": [{"subitem_select_item": "author"}]}, "item_6_source_id_35": {"attribute_name": "ISSN", "attribute_value_mlt": [{"subitem_source_identifier": "0040-4039", "subitem_source_identifier_type": "ISSN"}]}, "item_6_source_id_39": {"attribute_name": "NII ISSN", "attribute_value_mlt": [{"subitem_source_identifier": "0040-4039", "subitem_source_identifier_type": "ISSN"}]}, "item_6_source_id_40": {"attribute_name": "\u66f8\u8a8c\u30ec\u30b3\u30fc\u30c9ID", "attribute_value_mlt": [{"subitem_source_identifier": "AA00861801", "subitem_source_identifier_type": "NCID"}]}, "item_6_text_69": {"attribute_name": "wosonly authkey", "attribute_value_mlt": [{"subitem_text_value": "Azulene; Indole; Coupling reaction; Electrophilic substitution"}]}, "item_6_text_70": {"attribute_name": "wosonly keywords", "attribute_value_mlt": [{"subitem_text_value": "SUBSTITUTED BENZENE-DERIVATIVES; LIQUID-CRYSTALLINE BEHAVIOR; N-CONTAINING HETEROCYCLES; FISCHER INDOLE SYNTHESIS; CROSS-COUPLING REACTION; REDOX BEHAVIOR; ELECTROPHILIC SUBSTITUTION; AZULENE; STRATEGY; ACCESS"}]}, "item_6_textarea_68": {"attribute_name": "wosonly abstract", "attribute_value_mlt": [{"subitem_textarea_value": "Azulene derivatives reacted with 2-indolinones in the presence of triflic anhydride (Tf2O) to afford 1-(indo1-2-yl)azulenes in good yields. In the cases of the reaction of 6-tert-butyl-1-(methylthio)azulene (11) and 1-(1,4-dihydropyridin-4-yl)azulene 14, 1,1\u0027-biazulene derivative 24 and 1-(indo1-2-yl)azulene (2) were obtained under the similar reaction conditions, respectively, instead of the presumed electrophilic substitution products. (C) 2012 Elsevier Ltd. All rights reserved."}]}, "item_creator": {"attribute_name": "\u8457\u8005", "attribute_type": "creator", "attribute_value_mlt": [{"creatorNames": [{"creatorName": "Shoji,  Taku"}], "nameIdentifiers": [{"nameIdentifier": "36224", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Inoue,  Yuta"}], "nameIdentifiers": [{"nameIdentifier": "36225", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Ito,  Shunji"}], "nameIdentifiers": [{"nameIdentifier": "36226", "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": "2015-09-28"}], "displaytype": "detail", "download_preview_message": "", "file_order": 0, "filename": "Tetrahedron Letters 53 (2012) 1493.pdf", "filesize": [{"value": "229.6 kB"}], "format": "application/pdf", "future_date_message": "", "is_thumbnail": false, "licensetype": "license_free", "mimetype": "application/pdf", "size": 229600.0, "url": {"label": "Tetrahedron Letters 53 (2012) 1493.pdf", "url": "https://soar-ir.repo.nii.ac.jp/record/11826/files/Tetrahedron Letters 53 (2012) 1493.pdf"}, "version_id": "eb43123c-0665-4380-8358-98beadc72163"}]}, "item_keyword": {"attribute_name": "\u30ad\u30fc\u30ef\u30fc\u30c9", "attribute_value_mlt": [{"subitem_subject": "Azulene", "subitem_subject_scheme": "Other"}, {"subitem_subject": "Indole", "subitem_subject_scheme": "Other"}, {"subitem_subject": "Coupling reaction", "subitem_subject_scheme": "Other"}, {"subitem_subject": "Electrophilic substitution", "subitem_subject_scheme": "Other"}]}, "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": "First synthesis of 1-(indo1-2-yl)azulenes by the Vilsmeier-Haack type arylation with triflic anhydride as an activating reagent", "item_titles": {"attribute_name": "\u30bf\u30a4\u30c8\u30eb", "attribute_value_mlt": [{"subitem_title": "First synthesis of 1-(indo1-2-yl)azulenes by the Vilsmeier-Haack type arylation with triflic anhydride as an activating reagent"}]}, "item_type_id": "6", "owner": "1", "path": ["1169/1170"], "permalink_uri": "http://hdl.handle.net/10091/16092", "pubdate": {"attribute_name": "\u516c\u958b\u65e5", "attribute_name_i18n": "\u516c\u958b\u65e5", "attribute_value": "2012-11-26"}, "publish_date": "2012-11-26", "publish_status": "0", "recid": "11826", "relation": {}, "relation_version_is_last": true, "title": ["First synthesis of 1-(indo1-2-yl)azulenes by the Vilsmeier-Haack type arylation with triflic anhydride as an activating reagent"], "weko_shared_id": null}