Synthesis of Bishomoinositols and an Entry for Construction of a Substituted 3-Oxabicyclo[3.3.1]nonane Skeleton
Özet
1,3,3a,7a-Tetrahydro-2-benzofuran was used as key compound for the synthesis of various bishomoinositol derivatives. The diene was subjected to an epoxidation reaction for further functionalization of the diene unit. The bisepoxide obtained was submitted to a ring-opening reaction with acid in the presence of water. Various bishomoinositols were synthesized. However, when the reaction was carried out in the presence of acetic anhydride, a substituted 3-oxabicyclo[3.3.1]nonane skeleton was formed. The mechanism of the formation of the products is discussed.
Atıf için künye
BARAN, A., Bekarlar, M., Aydin, G., NEBİOĞLU, M., Şahin, E., & Balci, M. (2012). Synthesis of Bishomoinositols and an Entry for Construction of a Substituted 3-Oxabicyclo[3.3.1]nonane Skeleton. JOURNAL OF ORGANIC CHEMISTRY, 77(3), 1244–1250. https://doi.org/10.1021/jo202494v
BibTeX
@article{baran2012-66600,
author = {BARAN, ARİF and Bekarlar, Merve and Aydin, Gokay and NEBİOĞLU, MEHMET and Şahin, Ertan and Balci, Metin},
title = {Synthesis of Bishomoinositols and an Entry for Construction of a Substituted 3-Oxabicyclo[3.3.1]nonane Skeleton},
journal = {JOURNAL OF ORGANIC CHEMISTRY},
year = {2012},
volume = {77},
number = {3},
pages = {1244--1250},
issn = {0022-3263},
doi = {10.1021/jo202494v},
url = {https://akademik.atauni.edu.tr/yayinlar/66600-synthesis-of-bishomoinositols-and-an-entry-for-construction-of-a-substituted-3}
}