Access to polysubstituted naphthalenes and anthracenes via a retro-Diels Alder reaction
Yazarlar (4)
Esra Turan Akın
Atatürk Üniversitesi, Türkiye
Doç. Dr. Musa ERDOĞAN
Kafkas Üniversitesi, Türkiye
Arif Daştan
Atatürk Üniversitesi, Türkiye
Nurullah Saraçoğlu
Atatürk Üniversitesi, Türkiye
| Makale Türü | Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale) | ||
| Dergi Adı | Tetrahedron | ||
| Dergi ISSN | 0040-4020 Wos Dergi Scopus Dergi | ||
| Dergi Tarandığı Indeksler | SCI-Expanded | ||
| Makale Dili | İngilizce | Basım Tarihi | 09-2017 |
| Cilt / Sayı / Sayfa | 73 / 37 / 5537–5546 | DOI | 10.1016/j.tet.2017.07.058 |
| Makale Linki | http://dx.doi.org/10.1016/j.tet.2017.07.058 | ||
| Özet |
| Naphthalene and anthracene nuclei are present in several natural and synthetic compounds. Due to their unique physical and chemical properties, access to functionalized naphthalenes and anthracenes has attracted the attention of both synthetic and medicinal chemists over the decades. In this study, successive Diels–Alder/retro-Diels–Alder reactions of dimethyl 1,2,4,5-tetrazine-3,6-dicarboxylate with various bicyclic alkenes in one pot to yield naphthalene and anthracene derivatives are reported. Using anti- and syn-cyclotrimers derived from the cyclotrimerization of benzobarrelene as alkene partner enabled efficient synthesis of trinaphthylene. |
| Anahtar Kelimeler |
| Tetrazine | retro-Diels-Alder | Naphthalene | Anthracene |
Science Direct
Access to polysubstituted naphthalenes and anthracenes via a retro-Diels Alder reaction
BM Sürdürülebilir Kalkınma Amaçları
| Atıf Sayıları | |
| WoS | 16 |
| SCOPUS | 19 |
| Google Scholar | 23 |