Makale
Tam Makale
Uluslararası
2002
Bromination of 2,3-dibromobenzobarrelene at different conditions: Highly brominated benzobicyclic systems
TURKISH JOURNAL OF CHEMISTRY
Cilt 26 · Sayı 4 · ss. 535–546 · 01.01.2002
Özet
The electrophilic addition of bromine to 2,3-dibromobenzobarrelene at 10degreesC led to the formation of completely rearranged products in high yield. Bromination of 2,3-dibromobenzobarrelene with molecular bromine in decalin at 150degreesC and with DBTCE in CCl(4) at 77degreesC gave rearranged and non-rearranged products. The radical and ionic mechanism are discussed. All compounds were characterized properly. by NMR spectroscopy and chemical transformation.
Atıf için künye
Daştan, A. (2002). Bromination of 2,3-dibromobenzobarrelene at different conditions: Highly brominated benzobicyclic systems. TURKISH JOURNAL OF CHEMISTRY, 26(4), 535–546.
BibTeX
@article{dastan2002-70679,
author = {Daştan, Arif},
title = {Bromination of 2,3-dibromobenzobarrelene at different conditions: Highly brominated benzobicyclic systems},
journal = {TURKISH JOURNAL OF CHEMISTRY},
year = {2002},
volume = {26},
number = {4},
pages = {535--546},
issn = {1300-0527},
url = {https://akademik.atauni.edu.tr/yayinlar/70679-bromination-of-23-dibromobenzobarrelene-at-different-conditions-highly}
}