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Facile synthesis of indolizino[3,4,5-ab]isoindoles by an acid-induced cyclization of 1,2-di(1H-pyrrol-2-yl)benzenes

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dc.contributor.author Kuzuhara, Daiki en
dc.contributor.author Miyake, Satoshi en
dc.contributor.author Moriyama, Hirotake en
dc.contributor.author Tamura, Yuto en
dc.contributor.author Aratani, Naoki en
dc.contributor.author Yamada, Hiroko en
dc.date.accessioned 2017-08-08T04:57:32Z en
dc.date.available 2017-08-08T04:57:32Z en
dc.date.issued 2015-10-07 en
dc.identifier.issn 0040-4039 en
dc.identifier.uri http://hdl.handle.net/10061/12068 en
dc.description.abstract The new synthetic method of indolizino[3,4,5-ab]isoindoles (INIs) by an acid-induced intramolecular cyclization of 1,2-di(1H-pyrrol-2-yl)benzenes has been developed. This protocol can be applied to the preparation of INI derivatives with electron-donating and -withdrawing groups as well as azaINIs. en
dc.language.iso en en
dc.publisher Elsevier en
dc.relation.isversionof http://www.sciencedirect.com/science/article/pii/S0040403915013465 en
dc.rights Copyright c 2015 Elsevier Ltd. en
dc.rights 出版社許諾条件により本文は2017/10/7以降に公表する。 ja
dc.subject Indolizino[3,4,5-ab]isoindoles en
dc.subject Cyclization en
dc.subject Acid en
dc.subject 1,2-Di(1H-pyrrol-2-yl)benzene en
dc.subject Fluorescence en
dc.title Facile synthesis of indolizino[3,4,5-ab]isoindoles by an acid-induced cyclization of 1,2-di(1H-pyrrol-2-yl)benzenes en
dc.type.nii Journal Article en
dc.contributor.transcription クズハラ, ダイキ ja
dc.contributor.transcription アラタニ, ナオキ ja
dc.contributor.transcription ヤマダ, ヒロコ ja
dc.contributor.alternative 葛原, 大軌 ja
dc.contributor.alternative 荒谷, 直樹 ja
dc.contributor.alternative 山田, 容子 ja
dc.textversion author en
dc.identifier.ncid AA11539822 en
dc.identifier.jtitle Tetrahedron Letters en
dc.identifier.volume 56 en
dc.identifier.issue 41 en
dc.identifier.spage 5564 en
dc.identifier.epage 5567 en
dc.relation.doi 10.1016/j.tetlet.2015.08.044 en
dc.identifier.NAIST-ID 73296204 en
dc.identifier.NAIST-ID 73299042 en
dc.identifier.NAIST-ID 73293565 en


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