Makale
Tam Makale
Uluslararası
1996
A novel and stereospecific synthesis of conduritol-E via cyclohexa-3,5-diene-1,2-diol
TURKISH JOURNAL OF CHEMISTRY
Cilt 20 · Sayı 4 · ss. 341–344 · 01.01.1996
Özet
Conduritol-E was synthesized starting from cyclohexa-3,5-diene-1,2-diol la in six steps. Acetylation of the diol la followed by bromination gave (2 alpha/1 beta, 3 beta, 4 beta)-1,2-dibromo-2,3-diacetoxy-5-cyclohexene 3 as main product. KMnO4-hydoxylation of the dibromide 3 followed by acetylation, Zn-elimination and hydrolysis afforded conduritol-E 5a.
Atıf için künye
Maraş, A., Seçen, H., SUTBEYAZ, Y., & BALCI, M. (1996). A novel and stereospecific synthesis of conduritol-E via cyclohexa-3,5-diene-1,2-diol. TURKISH JOURNAL OF CHEMISTRY, 20(4), 341–344.
BibTeX
@article{maras1996-71409,
author = {Maraş, Ahmet and Seçen, Hasan and SUTBEYAZ, Yaşar and BALCI, M},
title = {A novel and stereospecific synthesis of conduritol-E via cyclohexa-3,5-diene-1,2-diol},
journal = {TURKISH JOURNAL OF CHEMISTRY},
year = {1996},
volume = {20},
number = {4},
pages = {341--344},
issn = {1010-7614},
url = {https://akademik.atauni.edu.tr/yayinlar/71409-a-novel-and-stereospecific-synthesis-of-conduritol-e-via-cyclohexa-35-diene-12}
}