img
Highly diastereoselective synthesis of a novel functionalized triepoxytrinaphthylene      
Yazarlar
Doç. Dr. Musa ERDOĞAN
Kafkas Üniversitesi, Türkiye
Selçuk Eşsiz
Hakkari Üniversitesi, Türkiye
Fabrizio Fabris
Türkiye
Arif Daştan
Atatürk Üniversitesi, Türkiye
Özet
The high yielding synthesis of a novel benzocyclotrimer is herein presented. The syn-diastereomer is obtained as major product, presumably in virtue of the presence of an oxa-bridge of the bicylic components. The three oxa-bridges can be used for further functionalization, as well as the six bromine atoms of the three aromatic rings, as demonstrated in the aromatization of a mixture of anti-1 and syn-1 (3:7) leading to trinaphthylene.
Anahtar Kelimeler
Cyclotrimerization | copper | cup-shaped molecules | stereoselective reactions | aromatic compounds
Makale Türü Özgün Makale
Makale Alt Türü SSCI, AHCI, SCI, SCI-Exp dergilerinde yayımlanan tam makale
Dergi Adı ARKIVOC
Dergi ISSN 1551-7004
Dergi Tarandığı Indeksler SCI-Expanded
Makale Dili İngilizce
Basım Tarihi 1-2018
Cilt No 2018
Sayı 3
Sayfalar 134 / 143
Doi Numarası 10.24820/ark.5550190.p010.408
Makale Linki https://doi.org/10.24820/ark.5550190.p010.408
BM Sürdürülebilir Kalkınma Amaçları
Atıf Sayıları
Highly diastereoselective synthesis of a novel functionalized triepoxytrinaphthylene

Paylaş