{"created":"2023-05-15T12:35:34.622497+00:00","id":4539,"links":{},"metadata":{"_buckets":{"deposit":"8106e54d-0cb2-4fa4-b7c8-3587b97942fa"},"_deposit":{"created_by":3,"id":"4539","owners":[3],"pid":{"revision_id":0,"type":"depid","value":"4539"},"status":"published"},"_oai":{"id":"oai:nitech.repo.nii.ac.jp:00004539","sets":["31"]},"author_link":["14150","14154","14148","14156","14149","14153","14151","14152","10534","14147","8643","14146"],"item_10001_biblio_info_28":{"attribute_name":"書誌情報","attribute_value_mlt":[{"bibliographicIssueDates":{"bibliographicIssueDate":"1998-01-01","bibliographicIssueDateType":"Issued"},"bibliographicIssueNumber":"7","bibliographicPageEnd":"1303","bibliographicPageStart":"1299","bibliographicVolumeNumber":"1998","bibliographic_titles":[{"bibliographic_title":"Journal of the Chemical Society. Perkin transactions 1 : organic and bio-organic chemistry."}]}]},"item_10001_description_36":{"attribute_name":"内容記述","attribute_value_mlt":[{"subitem_description":"Three cyclomaltoheptaoses (1, 2 and 3) which possess a benzyloxycarbonylamino group, a tert-butoxycarbonylamino group or an azido group, and six tosyloxy groups, on their C-6 atoms have been prepared. These can be versatile intermediates for the synthesis of derivatives possessing an amino group as well as other functional groups. As an example of their derivatization, their conversion to compounds containing 3,6-anhydroglucoses, which possess cation-binding abilities, is also reported.","subitem_description_type":"Other"}]},"item_10001_description_38":{"attribute_name":"フォーマット","attribute_value_mlt":[{"subitem_description":"application/pdf","subitem_description_type":"Other"}]},"item_10001_full_name_27":{"attribute_name":"著者別名","attribute_value_mlt":[{"nameIdentifiers":[{},{}],"names":[{"name":"山村, 初雄"}]},{"nameIdentifiers":[{}],"names":[{"name":"荒木, 修喜"}]}]},"item_10001_publisher_29":{"attribute_name":"出版者","attribute_value_mlt":[{"subitem_publisher":"Royal Society of Chemistry"}]},"item_10001_relation_34":{"attribute_name":"DOI","attribute_value_mlt":[{"subitem_relation_name":[{"subitem_relation_name_text":"10.1039/A707953B"}],"subitem_relation_type":"isIdenticalTo","subitem_relation_type_id":{"subitem_relation_type_id_text":"http://dx.doi.org/10.1039/A707953B","subitem_relation_type_select":"DOI"}}]},"item_10001_source_id_30":{"attribute_name":"ISSN","attribute_value_mlt":[{"subitem_source_identifier":"0300922X","subitem_source_identifier_type":"ISSN"}]},"item_10001_source_id_32":{"attribute_name":"書誌レコードID（NCID）","attribute_value_mlt":[{"subitem_source_identifier":"AA00695134","subitem_source_identifier_type":"NCID"}]},"item_10001_version_type_33":{"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":"Yamamura, Hatsuo","creatorNameLang":"en"}],"nameIdentifiers":[{},{}]},{"creatorNames":[{"creatorName":"Yotsuya, Tadahiro","creatorNameLang":"en"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Usami, Satoshi","creatorNameLang":"en"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Iwasa, Akihito","creatorNameLang":"en"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Ono, Shoji","creatorNameLang":"en"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Tanabe, Yoshihisa","creatorNameLang":"en"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Iida, Daisuke","creatorNameLang":"en"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Katsuhara, Takao","creatorNameLang":"en"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Kano, Kazuaki","creatorNameLang":"en"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Uchida, Tetsuo","creatorNameLang":"en"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Araki, Shuki","creatorNameLang":"en"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Kawai, Masao","creatorNameLang":"en"}],"nameIdentifiers":[{}]}]},"item_files":{"attribute_name":"ファイル情報","attribute_type":"file","attribute_value_mlt":[{"accessrole":"open_date","date":[{"dateType":"Available","dateValue":"2017-01-23"}],"displaytype":"detail","filename":"JCSP 1998_1299.pdf","filesize":[{"value":"133.5 kB"}],"format":"application/pdf","license_note":"J. Chem. Soc., Perkin Trans. 1, 1998, 1299-1303 -Reproduced by permission of The Royal Society of Chemistry (RSC)","licensetype":"license_note","mimetype":"application/pdf","url":{"label":"本文_fulltext","url":"https://nitech.repo.nii.ac.jp/record/4539/files/JCSP 1998_1299.pdf"},"version_id":"c2fa9764-4cba-4354-bb99-296d8f7aa643"}]},"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":"Primary hydroxy-modified cyclomaltoheptaose derivatives with two kinds of substituents. Preparation of 6I-(benzyloxycarbonylamino)-, 6I-(tert-butoxycarbonylamino)- and 6I-azido-6I-deoxy-6II,6III,6IV, 6V,6VI,6VII-hexa-O-tosylcyclomaltoheptaose and their conversion to the hexakis-(3,6-anhydro) derivatives","item_titles":{"attribute_name":"タイトル","attribute_value_mlt":[{"subitem_title":"Primary hydroxy-modified cyclomaltoheptaose derivatives with two kinds of substituents. Preparation of 6I-(benzyloxycarbonylamino)-, 6I-(tert-butoxycarbonylamino)- and 6I-azido-6I-deoxy-6II,6III,6IV, 6V,6VI,6VII-hexa-O-tosylcyclomaltoheptaose and their conversion to the hexakis-(3,6-anhydro) derivatives","subitem_title_language":"en"}]},"item_type_id":"10001","owner":"3","path":["31"],"pubdate":{"attribute_name":"公開日","attribute_value":"2012-11-06"},"publish_date":"2012-11-06","publish_status":"0","recid":"4539","relation_version_is_last":true,"title":["Primary hydroxy-modified cyclomaltoheptaose derivatives with two kinds of substituents. Preparation of 6I-(benzyloxycarbonylamino)-, 6I-(tert-butoxycarbonylamino)- and 6I-azido-6I-deoxy-6II,6III,6IV, 6V,6VI,6VII-hexa-O-tosylcyclomaltoheptaose and their conversion to the hexakis-(3,6-anhydro) derivatives"],"weko_creator_id":"3","weko_shared_id":3},"updated":"2023-05-16T14:17:45.027629+00:00"}