2024-03-29T14:51:33Z
https://nagoya.repo.nii.ac.jp/oai
oai:nagoya.repo.nii.ac.jp:00029317
2023-01-16T04:29:11Z
1939:1940:1941
Highly Selective Synthesis of Tetrahydronaphthaleno[60]fullerenes via Fullerene-Cation-Mediated Intramolecular Cyclization
Yang, Xiao-Yu
Lin, Hao-Sheng
Matsuo, Yutaka
open access
“This document is the Accepted Manuscript version of a Published Work that appeared in final form in [The Journal of Organic Chemistry], copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see [https://pubs.acs.org/articlesonrequest/AOR-I2eCpwRbQgNN8JJNvNNb].”
Mixtures
Carbon nanomaterials
Nanospheres
Solutions
Solubility
A high-yielding protocol to construct six-membered carbon rings on fullerene is presented. This methodology with in situ fullerene-cation-mediated intramolecular cyclization provides high selectivity and efficient access to six-membered tetrahydronaphthaleno[60]fullerenes with a remarkable functional group tolerance and excellent yields. Furthermore, high solubilities of tetrahydronaphthaleno[60]fullerenes are reported.
ファイル公開:2020-12-20
ACS Publications
2019-12-20
eng
journal article
AM
http://hdl.handle.net/2237/00031504
https://nagoya.repo.nii.ac.jp/records/29317
https://doi.org/10.1021/acs.joc.9b02618
0022-3263
The Journal of Organic Chemistry
84
24
16314
16322
https://nagoya.repo.nii.ac.jp/record/29317/files/6mem cation JOC matsuo.pdf
application/pdf
1.6 MB
2020-12-20