Abstract
An efficient iron/acetic acid mediated one pot reductive cyclization protocol was successfully developed for the synthesis of acridinone and quinoline derivatives. This highly efficient process proceeds under mild conditions, tolerates different functional groups, and provides various substituted acridinone and quinoline derivatives in good to excellent yields. In addition, biologically active compounds also accessed from this method.
| Original language | English |
|---|---|
| Pages (from-to) | 37806-37811 |
| Number of pages | 6 |
| Journal | RSC Advances |
| Volume | 4 |
| Issue number | 71 |
| DOIs | |
| Publication status | Published - 2014 Jan 1 |
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ASJC Scopus subject areas
- Chemistry(all)
- Chemical Engineering(all)
Cite this
Iron/acetic acid mediated intermolecular tandem C-C and C-N bond formation : An easy access to acridinone and quinoline derivatives. / Rajawinslin, R. R.; Gawande, Sachin D.; Kavala, Veerababurao; Huang, Yi Hsiang; Kuo, Chun Wei; Kuo, Ting Shen; Chen, Mei Ling; He, Chiu Hui; Yao, Ching Fa.
In: RSC Advances, Vol. 4, No. 71, 01.01.2014, p. 37806-37811.Research output: Contribution to journal › Article
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TY - JOUR
T1 - Iron/acetic acid mediated intermolecular tandem C-C and C-N bond formation
T2 - An easy access to acridinone and quinoline derivatives
AU - Rajawinslin, R. R.
AU - Gawande, Sachin D.
AU - Kavala, Veerababurao
AU - Huang, Yi Hsiang
AU - Kuo, Chun Wei
AU - Kuo, Ting Shen
AU - Chen, Mei Ling
AU - He, Chiu Hui
AU - Yao, Ching Fa
PY - 2014/1/1
Y1 - 2014/1/1
N2 - An efficient iron/acetic acid mediated one pot reductive cyclization protocol was successfully developed for the synthesis of acridinone and quinoline derivatives. This highly efficient process proceeds under mild conditions, tolerates different functional groups, and provides various substituted acridinone and quinoline derivatives in good to excellent yields. In addition, biologically active compounds also accessed from this method.
AB - An efficient iron/acetic acid mediated one pot reductive cyclization protocol was successfully developed for the synthesis of acridinone and quinoline derivatives. This highly efficient process proceeds under mild conditions, tolerates different functional groups, and provides various substituted acridinone and quinoline derivatives in good to excellent yields. In addition, biologically active compounds also accessed from this method.
UR - http://www.scopus.com/inward/record.url?scp=84906861565&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84906861565&partnerID=8YFLogxK
U2 - 10.1039/c4ra06410k
DO - 10.1039/c4ra06410k
M3 - Article
AN - SCOPUS:84906861565
VL - 4
SP - 37806
EP - 37811
JO - RSC Advances
JF - RSC Advances
SN - 2046-2069
IS - 71
ER -