{"_buckets": {"deposit": "540aff89-bf51-45cd-b269-e0e7683bda80"}, "_deposit": {"id": "24635", "owners": [], "pid": {"revision_id": 0, "type": "depid", "value": "24635"}, "status": "published"}, "_oai": {"id": "oai:nagoya.repo.nii.ac.jp:00024635"}, "item_10_biblio_info_6": {"attribute_name": "\u66f8\u8a8c\u60c5\u5831", "attribute_value_mlt": [{"bibliographicIssueDates": {"bibliographicIssueDate": "2017-05-08", "bibliographicIssueDateType": "Issued"}, "bibliographicIssueNumber": "20", "bibliographicPageEnd": "5497", "bibliographicPageStart": "5494", "bibliographicVolumeNumber": "56", "bibliographic_titles": [{"bibliographic_title": "ANGEWANDTE CHEMIE-INTERNATIONAL EDITION"}]}]}, "item_10_description_4": {"attribute_name": "\u6284\u9332", "attribute_value_mlt": [{"subitem_description": "In the presence of a cationic Ru catalyst, 1,6-diynes bearing a terminal styryl moiety underwent [2+2+2] cyclization to produce dehydrobiphenylenes fused with a five-membered ring. Although the cycloadducts were unstable toward purification, their one-pot iodine-mediated ring expansion successfully afforded unprecedented bridged ketone products containing a benzo-fused bicyclo[3.2.1] framework.", "subitem_description_type": "Abstract"}]}, "item_10_identifier_60": {"attribute_name": "URI", "attribute_value_mlt": [{"subitem_identifier_type": "DOI", "subitem_identifier_uri": "http://doi.org/10.1002/anie.201700493"}, {"subitem_identifier_type": "HDL", "subitem_identifier_uri": "http://hdl.handle.net/2237/26853"}]}, "item_10_publisher_32": {"attribute_name": "\u51fa\u7248\u8005", "attribute_value_mlt": [{"subitem_publisher": "Wiley"}]}, "item_10_rights_12": {"attribute_name": "\u6a29\u5229", "attribute_value_mlt": [{"subitem_rights": "\"This is the peer reviewed version of the following article: [Y. Yamamoto, K.-i. Nishimura, S. Mori, M. Shibuya, Angew. Chem. Int. Ed. 2017, 56, 5494.], which has been published in final form at [http://doi.org/10.1002/anie.201700493]. 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