118666-03-8Relevant articles and documents
Utilization of cyanopyridine in design and synthesis of first-in-class anticancer dual acting PIM-1 kinase/HDAC inhibitors
Bass, Amr K.A.,Nageeb, El-Shimaa M.,El-Zoghbi, Mona S.,Mohamed, Mamdouh F.A.,Badr, Mohamed,Abuo-Rahma, Gamal El-Din A.
, (2021/12/27)
Herein, we report design and synthesis of twenty-one dual PIM-1/HDAC inhibitors utilizing 3-cyanopyridines as a novel cap moiety linked with aliphatic /aromatic linker bearing carboxylic acid 3a-g, hydroxamic acid 4a-g or 2-aminoanilide moieties 5a-g as z
Efficient Approach to the Synthesis of Ethyl 3-Amino-4,6-diarylfuro[2,3-b] pyridine-2-carboxylate
Shah, Hetal C.,Shah, Vaishali H.,Desai, Nirmal D.
experimental part, p. 3126 - 3140 (2009/12/01)
Novel ethyl 3-amino-4,6-diarylfuro[2,3-b]pyridine-2-carboxylate were synthesized by Thorpe-Ziegler cyclization using solid-liquid phase-transfer catalysis conditions.
Synthesis of 4-oxo-4H-pyrido[3',2':4,5]furo [3,2-d]-(1,3)oxazines
Wagner,Prantz
, p. 213 - 214 (2007/10/02)
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