Synthesis of dipyrrolo[2,3-a:1 ',2 ',3 '-fg]acridin-12(1H)-ones
dc.authorid | 0000-0002-7347-2223 | |
dc.authorid | 0000-0001-9386-4892 | |
dc.authorid | 0000-0002-0951-9621 | |
dc.authorid | 0000-0002-5526-4359 | |
dc.authorscopusid | 7103099188 | |
dc.authorscopusid | 55326408200 | |
dc.authorscopusid | 7003524216 | |
dc.authorscopusid | 55308985300 | |
dc.authorscopusid | 36788078200 | |
dc.authorscopusid | 57195515398 | |
dc.authorscopusid | 16833488100 | |
dc.authorwosid | k, h/ABA-1339-2020 | |
dc.authorwosid | Sengul, Ibrahim Fazil/AAG-4368-2019 | |
dc.contributor.author | Beyer, Renee L. | |
dc.contributor.author | Kandemir, Hakan | |
dc.contributor.author | Bhadbhade, Mohan | |
dc.contributor.author | Şengül, İbrahim Fazıl | |
dc.contributor.author | Leu, Chao-Wei | |
dc.contributor.author | Wenholz, Daniel S. | |
dc.contributor.author | Black, David StC. | |
dc.date.accessioned | 2022-05-11T14:30:59Z | |
dc.date.available | 2022-05-11T14:30:59Z | |
dc.date.issued | 2018 | |
dc.department | Fakülteler, Fen Edebiyat Fakültesi, Kimya Bölümü | |
dc.description.abstract | Acylation reactions of 4,6-dimethoxyindoles with glyoxyloyl chlorides were achieved by the use of graphite powder in 1,2-dichloroethane at reflux. The products were monoketones as a result of decarbonylation, rather than the expected 1,2-diketones. Treatment of these monoketones with base led to their cyclisation and elimination of methanol to afford the novel dipyrrolo[2.3-a:1',2',3'-fg]acridin-12(1H)-ones. (C) 2018 Elsevier Ltd. All rights reserved. | |
dc.description.sponsorship | University of New South Wales; Turkish GovernmentTurkiye Bilimsel ve Teknolojik Arastirma Kurumu (TUBITAK) | |
dc.description.sponsorship | We thank the University of New South Wales and the Turkish Government for financial support. | |
dc.identifier.doi | 10.1016/j.tetlet.2018.11.011 | |
dc.identifier.endpage | 4486 | |
dc.identifier.issn | 0040-4039 | |
dc.identifier.issue | 51 | en_US |
dc.identifier.scopus | 2-s2.0-85056411840 | |
dc.identifier.scopusquality | Q3 | |
dc.identifier.startpage | 4483 | |
dc.identifier.uri | https://doi.org/10.1016/j.tetlet.2018.11.011 | |
dc.identifier.uri | https://hdl.handle.net/20.500.11776/7270 | |
dc.identifier.volume | 59 | |
dc.identifier.wos | WOS:000453495800009 | |
dc.identifier.wosquality | Q2 | |
dc.indekslendigikaynak | Web of Science | |
dc.indekslendigikaynak | Scopus | |
dc.institutionauthor | Kandemir, Hakan | |
dc.language.iso | en | |
dc.publisher | Pergamon-Elsevier Science Ltd | |
dc.relation.ispartof | Tetrahedron Letters | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.subject | Acylation | |
dc.subject | Decarbonylation | |
dc.subject | Acridones | |
dc.subject | Indoles | |
dc.subject | Pyrroloindoles | |
dc.subject | Pyrroloacridones | |
dc.subject | Indoles | |
dc.title | Synthesis of dipyrrolo[2,3-a:1 ',2 ',3 '-fg]acridin-12(1H)-ones | |
dc.type | Article |
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