Makale
Tam Makale
Uluslararası
1994
STEREOSPECIFIC SYNTHESIS OF CONDURAMINE-F4 AND CONDURITOL-F (LEUCANTHEMITOL)
SYNTHETIC COMMUNICATIONS
Cilt 24 · Sayı 15 · ss. 2103–2108 · 01.01.1994
Özet
Stereospecific synthesis of Conduramine-F4 and Conduritol-F has been achieved by fully stereospecific cyloaddition of singlet oxygen to cyclohexadiene ketal 1 followed by reductive extrusion of one oxygen atom. The obtained monoepoxide 3 has been smoothly opened to conduritol-F4 and conduramine-F4 6 by water and ammonia, respectively.
Atıf için künye
Seçen, H., GULTEKIN, S., SUTBEYAZ, Y., & BALCI, M. (1994). STEREOSPECIFIC SYNTHESIS OF CONDURAMINE-F4 AND CONDURITOL-F (LEUCANTHEMITOL). SYNTHETIC COMMUNICATIONS, 24(15), 2103–2108. https://doi.org/10.1080/00397919408010222
BibTeX
@article{secen1994-71398,
author = {Seçen, Hasan and GULTEKIN, Sena and SUTBEYAZ, Yaşar and BALCI, M},
title = {STEREOSPECIFIC SYNTHESIS OF CONDURAMINE-F4 AND CONDURITOL-F (LEUCANTHEMITOL)},
journal = {SYNTHETIC COMMUNICATIONS},
year = {1994},
volume = {24},
number = {15},
pages = {2103--2108},
issn = {0039-7911},
doi = {10.1080/00397919408010222},
url = {https://akademik.atauni.edu.tr/yayinlar/71398-stereospecific-synthesis-of-conduramine-f4-and-conduritol-f-leucanthemitol}
}