Gold-Catalyzed Formation of Pyrrolo- and Indolo-Oxazin Derivatives: the Key Structure of Some Marine Natural Products
| dc.authorid | Menges, Nurettin/0000-0002-5990-6275 | |
| dc.authorscopusid | 56768120400 | |
| dc.authorscopusid | 23973608700 | |
| dc.authorscopusid | 7006382595 | |
| dc.authorwosid | Menges, Nurettin/F-9678-2016 | |
| dc.contributor.author | Taskaya, Sultan | |
| dc.contributor.author | Menges, Nurettin | |
| dc.contributor.author | Balci, Metin | |
| dc.date.accessioned | 2025-05-10T17:37:47Z | |
| dc.date.available | 2025-05-10T17:37:47Z | |
| dc.date.issued | 2015 | |
| dc.department | T.C. Van Yüzüncü Yıl Üniversitesi | en_US |
| dc.department-temp | [Taskaya, Sultan; Menges, Nurettin; Balci, Metin] Middle E Tech Univ, Dept Chem, TR-06800 Ankara, Turkey; [Menges, Nurettin] Yuzuncu Yil Univ, Fac Pharm, TR-65100 Van, Turkey | en_US |
| dc.description | Menges, Nurettin/0000-0002-5990-6275 | en_US |
| dc.description.abstract | Various N-propargylpyrrole and indolecarboxylic acids were efficiently converted into 3,4-dihydropyrrolo- and indolo-oxazin-1-one derivatives by a gold(III)-catalyzed cyclization reaction. Some of the products underwent TFA-catalyzed double bond isomerization and some did not. Cyclization reactions in the presence of alcohol catalyzed by Au(I) resulted in the formation of hemiacetals after cascade reactions. | en_US |
| dc.description.sponsorship | Scientific and Technological Research Council of Turkey (TUBITAK) [TBAG-112 T360]; Turkish Academy of Sciences (TUBA); Middle East Technical University (METU) | en_US |
| dc.description.sponsorship | Financial support from the Scientific and Technological Research Council of Turkey (TUBITAK, Grant No. TBAG-112 T360), the Turkish Academy of Sciences (TUBA), and Middle East Technical University (METU) is gratefully acknowledged. | en_US |
| dc.description.woscitationindex | Science Citation Index Expanded | |
| dc.identifier.doi | 10.3762/bjoc.11.101 | |
| dc.identifier.endpage | 905 | en_US |
| dc.identifier.issn | 1860-5397 | |
| dc.identifier.pmid | 26124892 | |
| dc.identifier.scopus | 2-s2.0-84938767354 | |
| dc.identifier.scopusquality | Q2 | |
| dc.identifier.startpage | 897 | en_US |
| dc.identifier.uri | https://doi.org/10.3762/bjoc.11.101 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14720/14491 | |
| dc.identifier.volume | 11 | en_US |
| dc.identifier.wos | WOS:000355166500001 | |
| dc.identifier.wosquality | Q2 | |
| dc.language.iso | en | en_US |
| dc.publisher | Beilstein-institut | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
| dc.rights | info:eu-repo/semantics/openAccess | en_US |
| dc.subject | Alkyne Cyclization | en_US |
| dc.subject | Gold-Catalyzed Reaction | en_US |
| dc.subject | Indolo-Oxazin-1-One | en_US |
| dc.subject | Marine Natural Products | en_US |
| dc.subject | Pyrrolo-Oxazin-1-One | en_US |
| dc.title | Gold-Catalyzed Formation of Pyrrolo- and Indolo-Oxazin Derivatives: the Key Structure of Some Marine Natural Products | en_US |
| dc.type | Article | en_US |