| Makale Türü | Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale) | ||
| Dergi Adı | BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY (Q4) | ||
| Dergi ISSN | 1860-5397 Wos Dergi Scopus Dergi | ||
| Dergi Tarandığı Indeksler | SCI-Expanded | ||
| Makale Dili | İngilizce | Basım Tarihi | 12-2008 |
| Cilt / Sayı / Sayfa | 4 / 50 / 1–8 | DOI | 10.3762/bjoc.4.50 |
| Makale Linki | https://www.beilstein-journals.org/bjoc/articles/4/50 | ||
| Özet |
| When 9, 10-dibromoanthracene was treated with bromine in CCl 4 without a catalyst, 1, 2, 3, 4, 9, 10-hexabromo-1, 2, 3, 4-tetrahydroanthracene (3) was obtained in 95% yield in the absence of other stereoisomers or rearomatization products. We investigated the base-induced elimination reaction of hexabromide 3 under various conditions. Pyridine-induced elimination of hexabromide 3 afforded 2, 9, 10-tribromoanthracene (12) in 75% yield, and tribromide 12 was transformed to trimethoxy compound 13 and trinitrile 14 by copper-assisted nucleophilic substitution reactions. |
| Anahtar Kelimeler |
| anthracene derivative | bromination | bromoanthracene | cyanoanthracene | methoxyanthracene |
| Atıf Sayıları | |
| Google Scholar | 17 |
| Web of Science | 11 |
| Dergi Adı | Beilstein Journal of Organic Chemistry |
| Yayıncı | Beilstein-Institut Zur Forderung der Chemischen Wissenschaften |
| Açık Erişim | Evet |
| ISSN | 1860-5397 |
| E-ISSN | 1860-5397 |
| CiteScore | 3,8 |
| SJR | 0,482 |
| SNIP | 0,614 |