dc.contributor.author | Uludağ, Nesimi | |
dc.date.accessioned | 2022-05-11T14:31:04Z | |
dc.date.available | 2022-05-11T14:31:04Z | |
dc.date.issued | 2020 | |
dc.identifier.issn | 0034-7752 | |
dc.identifier.uri | https://doi.org/10.37358/RC.20.6.8173 | |
dc.identifier.uri | https://hdl.handle.net/20.500.11776/7305 | |
dc.description.abstract | A new and well planned approach has been accomplished for the total synthesis of 20-Deethyltubifolidine, which is effective for biological properties and fascinating molecules. This product embodies the ABCDE-ring system associated with the indole alkaloids. The synthesis was accomplished in six steps and produced a 38% yield. © 2020 SYSCOM 18 S.R.L.. All rights reserved. | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Syscom 18 SRL | en_US |
dc.identifier.doi | 10.37358/RC.20.6.8173 | |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | 20-deethyltubifolidine | en_US |
dc.subject | Azocino[4,3-b]indole | en_US |
dc.subject | Multi-step synthesis | en_US |
dc.subject | Tetrchloro-1,4-benzoquinone | en_US |
dc.title | Novel pathway for the synthesis of 20-deethyltubifolidine | en_US |
dc.type | article | en_US |
dc.relation.ispartof | Revista de Chimie | en_US |
dc.department | Fakülteler, Fen Edebiyat Fakültesi, Kimya Bölümü | en_US |
dc.identifier.volume | 71 | en_US |
dc.identifier.issue | 6 | en_US |
dc.identifier.startpage | 82 | en_US |
dc.identifier.endpage | 88 | en_US |
dc.institutionauthor | Uludağ, Nesimi | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.authorscopusid | 6507868758 | |
dc.identifier.scopus | 2-s2.0-85091568287 | en_US |