dc.contributor.author | Gollner, A. | en |
dc.contributor.author | Koutentis, Panayiotis Andreas | en |
dc.creator | Gollner, A. | en |
dc.creator | Koutentis, Panayiotis Andreas | en |
dc.date.accessioned | 2019-11-21T06:19:12Z | |
dc.date.available | 2019-11-21T06:19:12Z | |
dc.date.issued | 2010 | |
dc.identifier.issn | 1523-7060 | |
dc.identifier.uri | http://gnosis.library.ucy.ac.cy/handle/7/55516 | |
dc.description.abstract | "Chemical Equation Presented" Canthin-6-one (1) and nine analogues including the naturally occurring 9-methoxycanthin-6-one (2) and amaroridine (3) are prepared rapidly and in high yields via a convergent "non-classical" strategy that focuses on construction of the central ring B. The strategy relies on concomitant Pd-catalyzed Suzuki-Miyaura C-C coupling followed by a Cu-catalyzed C-N coupling that can be achieved either stepwise or in a new one-pot protocol starting from the appropriate 8-bromo-1,5-naphthyrldine. © 2010 American Chemical Society. | en |
dc.source | Organic letters | en |
dc.source.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-77949794863&doi=10.1021%2fol100300s&partnerID=40&md5=02ab4f2bd47622384ef467b2f4478f28 | |
dc.subject | article | en |
dc.subject | Indoles | en |
dc.subject | chemistry | en |
dc.subject | synthesis | en |
dc.subject | chemical structure | en |
dc.subject | copper | en |
dc.subject | catalysis | en |
dc.subject | indole derivative | en |
dc.subject | palladium | en |
dc.subject | Molecular Structure | en |
dc.subject | organometallic compound | en |
dc.subject | Organometallic Compounds | en |
dc.subject | naphthyridine derivative | en |
dc.subject | Amides | en |
dc.subject | stereoisomerism | en |
dc.subject | alkaloid | en |
dc.subject | Alkaloids | en |
dc.subject | amide | en |
dc.subject | canthin 6 one | en |
dc.subject | canthin-6-one | en |
dc.subject | Naphthyridines | en |
dc.title | Two-step total syntheses of Canthin-6-one alkaloids: New one-pot sequential Pd-catalyzed Suzuki-Miyaura coupling and Cu-catalyzed amidation reaction | en |
dc.type | info:eu-repo/semantics/article | |
dc.identifier.doi | 10.1021/ol100300s | |
dc.description.volume | 12 | |
dc.description.issue | 6 | |
dc.description.startingpage | 1352 | |
dc.description.endingpage | 1355 | |
dc.author.faculty | 002 Σχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences | |
dc.author.department | Τμήμα Χημείας / Department of Chemistry | |
dc.type.uhtype | Article | en |
dc.source.abbreviation | Org.Lett. | en |
dc.contributor.orcid | Koutentis, Panayiotis Andreas [0000-0002-4652-7567] | |
dc.gnosis.orcid | 0000-0002-4652-7567 | |