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Synthesis and SAR of 1,9-Dihydro-9-hydroxypyrazolo[3,4-b]quinolin-4-ones as Novel, Selective c-Jun N-Terminal Kinase Inhibitors.

✍ Scribed by Mei Liu; et al. et al.


Publisher
John Wiley and Sons
Year
2006
Weight
16 KB
Volume
37
Category
Article
ISSN
0931-7597

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## Abstract Efficient and direct protocols for the regioselective synthesis of the title compounds (IV) and (IX), resp., using multicomponent reactions of 5‐aminouracil (II) are given.