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Chemical Communications (Cambridge, England)|July 31, 2012
Ru-catalyzed hydrogenation of 3,5-diketo amides: simultaneous control of chemo- and enantioselectivityWanfang Li, Weizheng Fan, Xin Ma, et al.
Bioorganic & Medicinal Chemistry Letters|November 27, 2020
Pyrazolo[1,5-a]pyrimidine based Trk inhibitors: Design, synthesis, biological activity evaluationYongjie Zhang, Yan Liu, Ying Zhou, et al.
Chemical Biology & Drug Design|December 8, 2021
Synthesis and biological evaluation of novel 5,6-dihydrobenzo[h]quinazoline derivatives as FLT3 inhibitorsLei Ding, Qing Zhang, Kuantao Zhao, et al.
Bioorganic & Medicinal Chemistry Letters|March 1, 2022
Pyrizolo[1,5-a]pyrimidine derivatives of the second-generation TRK inhibitor: Design, synthesis and biological evaluationYiqing Fan, Yongjie Zhang, Yan Liu, et al.
Bioorganic & Medicinal Chemistry Letters|April 3, 2023
Design, synthesis and biological evaluation of quinazoline SOS1 inhibitorsHongyu Jiang, Yiqing Fan, Xia Wang, et al.
Bioorganic & Medicinal Chemistry Letters|February 8, 2024
Design, synthesis and biological evaluation of 2-phenylaminopyrimidine derivatives as EGFR inhibitorsChunlei Tang, Jie Wang, Dong Wang, et al.
Chemical Communications (Cambridge, England)|March 24, 2012
Acid-labile δ-ketal-β-hydroxy esters by asymmetric hydrogenation of corresponding δ-ketal-β-keto esters in the presence of CaCO3Weizheng Fan, Wanfang Li, Xin Ma, et al.
The Journal of Organic Chemistry|October 11, 2011
Ru-catalyzed asymmetric hydrogenation of γ-heteroatom substituted β-keto estersWeizheng Fan, Wanfang Li, Xin Ma, et al.
Bioorganic & Medicinal Chemistry Letters|February 2, 2026
Design, synthesis, and biological evaluation of cytochrome P450 CYP11A1 inhibitorsDongyu Wang, Shengkai Cui, Jingyi Yuan, et al.
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