Makale
Tam Makale
Uluslararası
2018
Highly diastereoselective synthesis of a novel functionalized triepoxytrinaphthylene
ARKIVOC
ss. 134–143 · 01.01.2018
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.
Atıf için künye
Erdogan, M., EŞSİZ, S., Fabris, F., & Daştan, A. (2018). Highly diastereoselective synthesis of a novel functionalized triepoxytrinaphthylene. ARKIVOC, 134–143. https://doi.org/10.24820/ark.5550190.p010.408
BibTeX
@article{erdogan2018-70697,
author = {Erdogan, Musa and EŞSİZ, Selçuk and Fabris, Fabrizio and Daştan, Arif},
title = {Highly diastereoselective synthesis of a novel functionalized triepoxytrinaphthylene},
journal = {ARKIVOC},
year = {2018},
pages = {134--143},
issn = {1551-7004},
doi = {10.24820/ark.5550190.p010.408},
url = {https://akademik.atauni.edu.tr/yayinlar/70697-highly-diastereoselective-synthesis-of-a-novel-functionalized}
}