Total Synthesis of Dictyodendrins A–F by the Gold‐Catalyzed Cascade Cyclization of Conjugated Diyne with Pyrrole

Matsuoka, Junpei; Inuki, Shinsuke; Matsuda, Yuka; Miyamoto, Yoichi; Otani, Mayumi; Oka, Masahiro; Oishi, Shinya; Ohno, Hiroaki

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http://hdl.handle.net/2433/268303

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DCフィールド	値	言語
dc.contributor.author	Matsuoka, Junpei	en
dc.contributor.author	Inuki, Shinsuke	en
dc.contributor.author	Matsuda, Yuka	en
dc.contributor.author	Miyamoto, Yoichi	en
dc.contributor.author	Otani, Mayumi	en
dc.contributor.author	Oka, Masahiro	en
dc.contributor.author	Oishi, Shinya	en
dc.contributor.author	Ohno, Hiroaki	en
dc.contributor.alternative	松岡, 純平	ja
dc.contributor.alternative	井貫, 晋輔	ja
dc.contributor.alternative	松田, 優佳	ja
dc.contributor.alternative	大石, 真也	ja
dc.contributor.alternative	大野, 浩章	ja
dc.date.accessioned	2022-03-04T08:41:08Z	-
dc.date.available	2022-03-04T08:41:08Z	-
dc.date.issued	2020-09-01	-
dc.identifier.uri	http://hdl.handle.net/2433/268303	-
dc.description.abstract	The total synthesis of dictyodendrins A–F was achieved using the gold(I)-catalyzed annulation of a conjugated diyne with NBoc-pyrrole for direct construction of the pyrrolo[2, 3-c]carbazole scaffold. Late-stage functionalization of the resulting pyrrolo[2, 3-c]carbazole to introduce various substituents provided divergent access to dictyodendrins. Some dictyodendrin analogues exhibited inhibitory activities toward CDK2/CycA2 and GSK3.	en
dc.language.iso	eng	-
dc.publisher	Wiley	en
dc.rights	This is the peer reviewed version of the following article: [J. Matsuoka, S. Inuki, Y. Matsuda, Y. Miyamoto, M. Otani, M. Oka, S. Oishi, H. Ohno, Chem. Eur. J. 2020, 26, 11064.], which has been published in final form at https://doi.org/10.1002/chem.202002563. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited.	en
dc.rights	The full-text file will be made open to the public on 09 August 2021 in accordance with publisher's 'Terms and Conditions for Self-Archiving'.	en
dc.rights	This is not the published version. Please cite only the published version. この論文は出版社版でありません。引用の際には出版社版をご確認ご利用ください。	en
dc.title	Total Synthesis of Dictyodendrins A–F by the Gold‐Catalyzed Cascade Cyclization of Conjugated Diyne with Pyrrole	en
dc.type	journal article	-
dc.type.niitype	Journal Article	-
dc.identifier.jtitle	Chemistry – A European Journal	en
dc.identifier.volume	26	-
dc.identifier.issue	49	-
dc.identifier.spage	11064	-
dc.identifier.epage	11064	-
dc.relation.doi	10.1002/chem.202002563	-
dc.textversion	author	-
dc.identifier.pmid	32776584	-
dcterms.accessRights	open access	-
datacite.date.available	2021-08-09	-
datacite.awardNumber	17H03971	-
datacite.awardNumber	18H04408	-
datacite.awardNumber	18J12107	-
datacite.awardNumber.uri	https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-17H03971/	-
datacite.awardNumber.uri	https://kaken.nii.ac.jp/grant/KAKENHI-PUBLICLY-18H04408/	-
datacite.awardNumber.uri	https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-18J12107/	-
dc.identifier.pissn	0947-6539	-
jpcoar.funderName	日本学術振興会	ja
jpcoar.funderName	日本学術振興会	ja
jpcoar.funderName	日本学術振興会	ja
jpcoar.awardTitle	多環式骨格構築反応を基軸とする生物活性インドールアルカロイドの全合成と創薬展開	ja
jpcoar.awardTitle	反応集積化によるアルカロイドの全合成と中分子化戦略	ja
jpcoar.awardTitle	金触媒を用いた連続反応を基盤とする新規複素環骨格構築法の開発と全合成への応用	ja
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