Maximizing the Benefits of Off-Target Kinase Inhibitor Activity
Author:
Publisher
American Association for Cancer Research (AACR)
Subject
Oncology
Cited by 9 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Chemoselective SN2′ Allylations of Detrifluoroacetylatively In Situ Generated 3-Fluoroindolin-2-one-Derived Tertiary Enolates with Morita–Baylis–Hillman Carbonates;The Journal of Organic Chemistry;2017-12-06
2. Polypharmacology in Precision Oncology: Current Applications and Future Prospects;Current Pharmaceutical Design;2017-01-24
3. Catalytic asymmetric aldol addition reactions of 3-fluoro-indolinone derived enolates;Organic & Biomolecular Chemistry;2017
4. Detrifluoroacetylative in Situ Generation of Free 3-Fluoroindolin-2-one-Derived Tertiary Enolates: Design, Synthesis, and Assessment of Reactivity toward Asymmetric Mannich Reactions;Organic Letters;2016-06-15
5. General asymmetric synthesis of 2,2,2-trifluoro-1-(1H-indol-3- and -2-yl)ethanamines;Journal of Fluorine Chemistry;2015-02
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