Abstract
The synthesis of unsymmetric functionalized pentacenes from 1,4-anthraquinones and functionalized isobenzofurans, which were prepared by transformation via C-H bond activation, was successfully accomplished. Examples of the synthesis of pentacenes with functional groups at the 5-position are still rare. These obtained functionalized pentacenes are highly soluble in hexane, toluene, and THF.
| Original language | English |
|---|---|
| Pages (from-to) | 5287-5289 |
| Number of pages | 3 |
| Journal | Organic Letters |
| Volume | 12 |
| Issue number | 22 |
| DOIs | |
| Publication status | Published - Nov 19 2010 |
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ASJC Scopus subject areas
- Organic Chemistry
- Physical and Theoretical Chemistry
- Biochemistry
Cite this
Synthesis of functionalized pentacenes from isobenzofurans derived from C-H bond activation. / Kuninobu, Yoichiro; Seiki, Takayuki; Kanamaru, Shunsuke; Nishina, Yuta; Takai, Kazuhiko.
In: Organic Letters, Vol. 12, No. 22, 19.11.2010, p. 5287-5289.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Synthesis of functionalized pentacenes from isobenzofurans derived from C-H bond activation
AU - Kuninobu, Yoichiro
AU - Seiki, Takayuki
AU - Kanamaru, Shunsuke
AU - Nishina, Yuta
AU - Takai, Kazuhiko
PY - 2010/11/19
Y1 - 2010/11/19
N2 - The synthesis of unsymmetric functionalized pentacenes from 1,4-anthraquinones and functionalized isobenzofurans, which were prepared by transformation via C-H bond activation, was successfully accomplished. Examples of the synthesis of pentacenes with functional groups at the 5-position are still rare. These obtained functionalized pentacenes are highly soluble in hexane, toluene, and THF.
AB - The synthesis of unsymmetric functionalized pentacenes from 1,4-anthraquinones and functionalized isobenzofurans, which were prepared by transformation via C-H bond activation, was successfully accomplished. Examples of the synthesis of pentacenes with functional groups at the 5-position are still rare. These obtained functionalized pentacenes are highly soluble in hexane, toluene, and THF.
UR - http://www.scopus.com/inward/record.url?scp=78449300397&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=78449300397&partnerID=8YFLogxK
U2 - 10.1021/ol102349r
DO - 10.1021/ol102349r
M3 - Article
C2 - 20961072
AN - SCOPUS:78449300397
VL - 12
SP - 5287
EP - 5289
JO - Organic Letters
JF - Organic Letters
SN - 1523-7060
IS - 22
ER -