Journal
JOURNAL OF COMBINATORIAL CHEMISTRY
Volume 11, Issue 5, Pages 809-812Publisher
AMER CHEMICAL SOC
DOI: 10.1021/cc800196u
Keywords
-
Funding
- National Science Foundation of China [20672090, 20810102050]
- Natural Science Foundation of the Jiangsu Province [BK2006033]
- Foundation of the Jiangsu Province [06-A-039]
- Open Foundation of Jiangsu Key Laboratory for Chemistry of Low-Dimensional Materials [JSKC07035]
- Qing Lan Project [08QLT001]
- Science & Technology Foundation of Xuzhou [XM08C027]
Ask authors/readers for more resources
A series of new heterocyclic compounds, involving pyrimido[4,5-b][1,6]-, benzo[b][1,6]-, pyrazolo[3,4-b][1,6]naphthyridine, and aza-benzo[b]fluorene skeletons were successfully synthesized via the reaction of structurally diverse 3,5-dibenzylidenepiperidin-4-one with various enamine-likes (2,6-diaminopyrimidin-4(3H)-one, 3-amino-5,5-dimethylcyclohex-2-enone, 3-methyl-1-phenyl-1H-pyrazol-5-amine and 1H-benzo-[d]imidazol-2-amine) in glycol under microwave irradiation. This method has the advantages of short synthetic route, operational simplicity, and increased safety for small-scale fast synthesis for biomedical screening.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available