Zhenyuan Miao

发表

Facile construction of structurally diverse thiazolidinedione-derived compounds via divergent stereoselective cascade organocatalysis and their biological exploratory studies.

Weiqi Wang, Shiping Zhu, Shengzheng Wang, 2013, ACS combinatorial science.

Divergent Cascade Construction of Skeletally Diverse “Privileged” Pyrazole‐Derived Molecular Architectures

Shengzheng Wang, Jian Li, Yongqiang Zhang, 2015 .

Facile assembly of chiral tetrahydrothiopyrans containing four consecutive stereocenters via an organocatalytic enantioselective Michael-Michael cascade.

Weiqi Wang, J. Li, Hao Li, 2014, Organic letters.

Enantioselective organocatalytic Michael addition of isorhodanines to α,β-unsaturated aldehydes.

Weiqi Wang, Yongqiang Zhang, Shanchao Wu, 2016, Organic & biomolecular chemistry.

Structure-based optimization of azole antifungal agents by CoMFA, CoMSIA, and molecular docking.

Min Zhang, Hui Xu, Youjun Zhou, 2006, Journal of medicinal chemistry.

Selection of evodiamine as a novel topoisomerase I inhibitor by structure-based virtual screening and hit optimization of evodiamine derivatives as antitumor agents.

Guoqiang Dong, Shengzheng Wang, Zhenyuan Miao, 2010, Journal of medicinal chemistry.

Design, synthesis and antifungal activity of isosteric analogues of benzoheterocyclic N-myristoyltransferase inhibitors.

Shengzheng Wang, Haitao Ji, Yongbing Cao, 2010, European journal of medicinal chemistry.

Discovery of benzothiazole derivatives as novel non-sulfamide NEDD8 activating enzyme inhibitors by target-based virtual screening.

Juan Wang, Zhenyuan Miao, Wannian Zhang, 2017, European journal of medicinal chemistry.

N-(7-Cyano-6-(4-fluoro-3-(2-(3-(trifluoromethyl)phenyl)acetamido)phenoxy)benzo[ d]thiazol-2-yl)cyclopropanecarboxamide (TAK-632) Analogues as Novel Necroptosis Inhibitors by Targeting Receptor-Interacting Protein Kinase 3 (RIPK3): Synthesis, Structure-Activity Relationships, and in Vivo Efficacy.

Xiaofei Chen, Zhenyuan Miao, Wannian Zhang, 2019, Journal of medicinal chemistry.

Small molecule-drug conjugates: A novel strategy for cancer-targeted treatment.

Zhenyuan Miao, Wannian Zhang, Chun-lin Zhuang, 2019, European journal of medicinal chemistry.

Scaffold Diversity Inspired by the Natural Product Evodiamine: Discovery of Highly Potent and Multitargeting Antitumor Agents.

Shengzheng Wang, Jian Li, Guoqiang Dong, 2015, Journal of medicinal chemistry.

Novel dual-mode antitumor chlorin-based derivatives as potent photosensitizers and histone deacetylase inhibitors for photodynamic therapy and chemotherapy.

Zhenyuan Miao, Jianzhong Yao, Wannian Zhang, 2021, European journal of medicinal chemistry.

Design and synthesis of novel water-soluble amino acid derivatives of chlorin p6 ethers as photosensitizer

Zhiqiang Ma, Zhenyuan Miao, Jianzhong Yao, 2019, Chinese Chemical Letters.

Amino acid derivatives of pyropheophorbide-a ethers as photosensitizer: Synthesis and photodynamic activity

Zhenyuan Miao, Jianzhong Yao, Wannian Zhang, 2016 .

Chalcone: A Privileged Structure in Medicinal Chemistry.

C. Xing, Zhenyuan Miao, Wannian Zhang, 2017, Chemical reviews.

Structure-based rational design, synthesis and antifungal activity of oxime-containing azole derivatives.

Shengzheng Wang, Haitao Ji, Yongbing Cao, 2010, Bioorganic & medicinal chemistry letters.

Synthesis via the Mannich Reaction and Biological Activity of Novel Fluorinated Camptothecin Derivatives

Zhenyuan Miao, Yuelin Wu, Chuanhao Wang, 2021, Chemistry of Heterocyclic Compounds.

Design, Synthesis and Biological Activity of (20S,21S)‐7‐Cyclohexyl‐21‐fluorocamptothecin Carbamates as Potential Antitumor Agents

Yuan Wang, Zhenyuan Miao, Jianzhong Yao, 2020, Chemistry & biodiversity.

Synthesis and biological activities of fluorinated 10-hydroxycamptothecin and SN38

Zhenyuan Miao, Jianzhong Yao, Wannian Zhang, 2014 .

Convenient synthesis of (2S,3R,4R,5S,6R)-2-(3-(4-ethylbenzyl)-4-chlorophenyl)-6-(hydroxymethyl)-tetrahydro-2H-pyran-3,4,5-triol

Zhenyuan Miao, Yonghai Liu, Da-li Li, 2008 .

Discovery of Novel Multiacting Topoisomerase I/II and Histone Deacetylase Inhibitors.

Wei Chen, Guoqiang Dong, Zhenyuan Miao, 2015, ACS medicinal chemistry letters.

New tricks for an old natural product: discovery of highly potent evodiamine derivatives as novel antitumor agents by systemic structure-activity relationship analysis and biological evaluations.

Shengzheng Wang, Yongqiang Zhang, Guoqiang Dong, 2012, Journal of medicinal chemistry.

Design, synthesis and biological evaluation of E-ring modified evodiamine derivatives as novel antitumor agents

Shiping Zhu, Guoqiang Dong, Zhenyuan Miao, 2014 .

Identification of the Raf kinase inhibitor TAK‐632 and its analogues as potent inhibitors of necroptosis by targeting RIPK1 and RIPK3

Hong-Yang Wang, Y. Chai, Xiaofei Chen, 2019, British journal of pharmacology.

Homobivalent, Trivalent, and Covalent PROTACs: Emerging Strategies for Protein Degradation.

Zhenyuan Miao, C. Sheng, Pei Wang, 2022, Journal of medicinal chemistry.

Synthesis and Biological Evaluation of Novel Homocamptothecins Conjugating with Dihydropyrimidine Derivatives as Potent Topoisomerase I Inhibitors

Shengzhang Wang, Wei Guo, Wenfeng Liu, 2011, Archiv der Pharmazie.

Design, synthesis, and biological evaluation of novel trimethoxyindole derivatives derived from natural products

Xiaodong Zhang, Zhenyuan Miao, Yuelin Wu, 2019, Monatshefte für Chemie - Chemical Monthly.

Novel non-trimethoxylphenyl piperlongumine derivatives selectively kill cancer cells.

Zhenyuan Miao, Wannian Zhang, Hao Ma, 2017, Bioorganic & medicinal chemistry letters.

Design, synthesis and biological activity of piperlongumine derivatives as selective anticancer agents.

Shiping Zhu, Shengzheng Wang, Shanchao Wu, 2014, European journal of medicinal chemistry.

BRDT Inhibitors for Male Contraceptive Drug Discovery: Current Status

G. Georg, Zhenyuan Miao, Xianghong Guan, 2018 .

From Antidiabetic to Antifungal: Discovery of Highly Potent Triazole–Thiazolidinedione Hybrids as Novel Antifungal Agents

Xiaomeng He, Shengzheng Wang, Yongqiang Zhang, 2014, ChemMedChem.

Discovery of highly potent triazoleantifungal agents with piperidine-oxadiazole side chains

Xiaomeng He, Yongqiang Zhang, Shanchao Wu, 2015 .

Total synthesis and structure–activity relationships of caspofungin-like macrocyclic antifungal lipopeptides

Shengzheng Wang, Guoqiang Dong, Zhenyuan Miao, 2012 .

Total synthesis and structure-activity relationships of new echinocandin-like antifungal cyclolipohexapeptides.

Zhenyuan Miao, Jianzhong Yao, Wannian Zhang, 2012, European journal of medicinal chemistry.

Novel carboline derivatives as potent antifungal lead compounds: design, synthesis, and biological evaluation.

Xiaomeng He, Shengzheng Wang, Jian Li, 2014, ACS medicinal chemistry letters.

Novel benzothiazole derivatives with a broad antifungal spectrum: design, synthesis and structure–activity relationships

Yongqiang Zhang, Shanchao Wu, Guoqiang Dong, 2013 .

Structure–activity relationships of tetrahydrocarbazole derivatives as antifungal lead compounds

Shiping Zhu, Shengzheng Wang, Yongqiang Zhang, 2013 .

Design, Synthesis, and Antifungal Activity of Novel Conformationally Restricted Triazole Derivatives

Haitao Ji, Zhenyuan Miao, Jianzhong Yao, 2009, Archiv der Pharmazie.

New azoles with potent antifungal activity: design, synthesis and molecular docking.

Haitao Ji, Yongbing Cao, Guoqiang Dong, 2009, European journal of medicinal chemistry.

Three-Dimensional Model of Lanosterol 14 (cid:2) -Demethylase from Cryptococcus neoformans : Active-Site Characterization and Insights into Azole Binding (cid:1) †

Guoqiang Dong, Zhenyuan Miao, Jianzhong Yao, 2009 .

The discovery and characterization of a novel scaffold as a potent hepatitis C virus inhibitor.

Shiping Zhu, Xiaonan Zhang, Guoqiang Dong, 2016, Chemical communications.

An alternative route for synthesis of o-trifluoroacetylanilines as useful fluorine-containing intermediates

Zhenyuan Miao, Jianzhong Yao, Wannian Zhang, 2010 .

New homocamptothecins: synthesis, antitumor activity, and molecular modeling.

M. Zhang, Haitao Ji, Zhenyuan Miao, 2008, Bioorganic & medicinal chemistry.

Trifluoromethyl-promoted homocamptothecins: synthesis and biological activity.

Wei Guo, Wenfeng Liu, Zhenyuan Miao, 2010, European journal of medicinal chemistry.

Design, synthesis and antifungal activity of carbazole derivatives

Shiping Zhu, Guoqiang Dong, Zhenyuan Miao, 2014 .

Discovery of highly potent novel antifungal azoles by structure-based rational design.

Haitao Ji, Yongbing Cao, Zhenyuan Miao, 2009, Bioorganic & medicinal chemistry letters.

Design and synthesis of antifungal benzoheterocyclic derivatives by scaffold hopping.

Shengzheng Wang, Yongbing Cao, Zhenyuan Miao, 2011, European journal of medicinal chemistry.

Meeting Organocatalysis with Drug Discovery: Asymmetric Synthesis of 3,3'-Spirooxindoles Fused with Tetrahydrothiopyrans as Novel p53-MDM2 Inhibitors.

Shengzheng Wang, Shanchao Wu, Guoqiang Dong, 2016, Organic letters.

Scaffold hopping of sampangine: discovery of potent antifungal lead compound against Aspergillus fumigatus and Cryptococcus neoformans.

Wei Chen, Guoqiang Dong, Zhenyuan Miao, 2014, Bioorganic & medicinal chemistry letters.

Synthesis and Pharmacological Evaluation of Novel Homocamptothecin-Dihydropyridine Derivative Conjugates as Potent Topoisomerase I Inhibitors

W. Guo, Wenfeng Liu, Zhenyuan Miao, 2011 .

Asymmetric synthesis of chiral dihydrothiopyrans via an organocatalytic enantioselective formal thio [3 + 3] cycloaddition reaction with binucleophilic bisketone thioethers.

Shiping Zhu, J. Li, Hao Li, 2013, Organic letters.

Structural Biology-Inspired Discovery of Novel KRAS-PDEδ Inhibitors.

Jian Li, Guoqiang Dong, Zhenyuan Miao, 2017, Journal of medicinal chemistry.

Design, Synthesis and Biological Evaluation of Sulfamide and Triazole Benzodiazepines as Novel p53-MDM2 Inhibitors

Guoqiang Dong, Zhenyuan Miao, Jianzhong Yao, 2014, International journal of molecular sciences.

Design, synthesis and antifungal activity of novel triazole derivatives containing substituted 1,2,3-triazole-piperdine side chains.

Shengzheng Wang, Guoqiang Dong, Zhenyuan Miao, 2014, European journal of medicinal chemistry.

Synthesis of novel benzoxanthone analogues as non-Camptothecin topoisomerase I inhibitors

Wei Guo, Wenfeng Liu, Yongqiang Zhang, 2012, Journal of enzyme inhibition and medicinal chemistry.

Three-Dimensional Model of Lanosterol 14α-Demethylase from Cryptococcus neoformans: Active-Site Characterization and Insights into Azole Binding

Haitao Ji, Wei Guo, Guoqiang Dong, 2009, Antimicrobial Agents and Chemotherapy.

Asymmetric Synthesis, Antifungal Activity and Molecular Modeling of Iodiconazole Isomers

Shengzheng Wang, Yongqiang Zhang, Zhenyuan Miao, 2013 .

Improved Model of Lanosterol 14α‐Demethylase by Ligand‐Supported Homology Modeling: Validation by Virtual Screening and Azole Optimization

Shengzheng Wang, Haitao Ji, Guoqiang Dong, 2010, ChemMedChem.

Chapter 1 – Topoisomerase I Inhibitors Derived from Natural Products: Structure–Activity Relationships and Antitumor Potency

Zhenyuan Miao, Wannian Zhang, C. Sheng, 2016 .

New strategies in the discovery of novel non-camptothecin topoisomerase I inhibitors.

Zhenyuan Miao, Wannian Zhang, C. Sheng, 2011, Current medicinal chemistry.

Novel conformationally restricted triazole derivatives with potent antifungal activity.

Shengzheng Wang, Yongbing Cao, Guoqiang Dong, 2010, European journal of medicinal chemistry.

Discovery of highly potent triazole antifungal derivatives by heterocycle-benzene bioisosteric replacement.

Shengzheng Wang, G. Fan, Guoqiang Dong, 2013, European journal of medicinal chemistry.

Design, synthesis and structure-activity relationships of new triazole derivatives containing N-substituted phenoxypropylamino side chains.

Shengzheng Wang, G. Jin, Yongqiang Zhang, 2012, European journal of medicinal chemistry.

Synthesis and evaluation of 9-benzylideneamino derivatives of homocamptothecin as potent inhibitors of DNA topoisomerase I.

Wei Guo, Wenfeng Liu, Zhenyuan Miao, 2010, European journal of medicinal chemistry.

Discovery of highly potent antifungal triazoles by structure-based lead fusion

Shengzheng Wang, Guoqiang Dong, Zhenyuan Miao, 2011 .

Design and synthesis of novel triazole antifungal derivatives by structure-based bioisosterism.

Shengzheng Wang, Yongbing Cao, Zhenyuan Miao, 2011, European journal of medicinal chemistry.

The discovery of novel antifungal scaffolds by structural simplification of the natural product sampangine.

Haiying He, Yuan-Ying Jiang, Guoqiang Dong, 2015, Chemical communications.

β‐Alanine‐DBU: A Highly Efficient Catalytic System for Knoevenagel‐Doebner Reaction under Mild Conditions

Zhenyuan Miao, Jianzhong Yao, Wannian Zhang, 2012 .

A novel drug discovery strategy: Mechanistic investigation of an enantiomeric antitumor agent targeting dual p53 and NF-κB pathways

Y. Sham, Guoqiang Dong, Zhenyuan Miao, 2014, Oncotarget.

Chemical Composition and Antidiabetic Activity of Opuntia Milpa Alta Extracts

C. Zheng, Zhenyuan Miao, Jianzhong Yao, 2010, Chemistry & biodiversity.

Chlorin p6-Based Water-Soluble Amino Acid Derivatives as Potent Photosensitizers for Photodynamic Therapy.

Buhong Li, Guoqiang Dong, Zou Tan, 2016, Journal of medicinal chemistry.

Novel pyropheophorbide a dimers: Synthesis and photobiological evaluation as potent photosensitizers for photodynamic therapy

Zhenyuan Miao, Jianzhong Yao, Xingjie Zhang, 2022, Journal of Molecular Structure.

Discovery of Novel 3,11‐Bispeptide Ester Arenobufagin Derivatives with Potential in Vivo Antitumor Activity and Reduced Cardiotoxicity

Zhenyuan Miao, Huojun Zhang, Yuelin Wu, 2023, Chemistry & biodiversity.

Discovery of 3-peptide substituted arenobufagin derivatives as potent antitumor agents with low cardiotoxicity

Yuan Wang, Zhenyuan Miao, Jianzhong Yao, 2020, Steroids.

Small molecules inhibiting Keap1-Nrf2 protein-protein interactions: a novel approach to activate Nrf2 function.

Zhenyuan Miao, Chunlin Zhuang, Zhongli Wu, 2017, MedChemComm.

Double-edged swords as cancer therapeutics: novel, orally active, small molecules simultaneously inhibit p53-MDM2 interaction and the NF-κB pathway.

Zhenyuan Miao, Jianzhong Yao, Wannian Zhang, 2014, Journal of medicinal chemistry.

Small Molecules Simultaneously Inhibiting p53-Murine Double Minute 2 (MDM2) Interaction and Histone Deacetylases (HDACs): Discovery of Novel Multitargeting Antitumor Agents.

Shanchao Wu, Guoqiang Dong, Zhenyuan Miao, 2018, Journal of medicinal chemistry.

A new strategy to improve the metabolic stability of lactone: discovery of (20S,21S)-21-fluorocamptothecins as novel, hydrolytically stable topoisomerase I inhibitors.

Shiping Zhu, Shengzheng Wang, Jian Li, 2013, Journal of medicinal chemistry.

Synthesis and Biological Assays of 9‐(Acylamino)homocamptothecins as DNA Topoisomerase I Inhibitors

Wei Guo, Wenfeng Liu, Guoqiang Dong, 2013, Chemistry & biodiversity.

Synthesis and preliminary bioevaluation of novel E-ring modified acetal analog of camptothecin as cytotoxic agents.

Shengzheng Wang, Yongqiang Zhang, Guoqiang Dong, 2012, European journal of medicinal chemistry.

Synthesis of 9‐(Heteroarylmethylidene)amino Derivatives of Homocamptothecin with Biological Activities

Wei Guo, Wenfeng Liu, Yongqiang Zhang, 2011, Chemistry & biodiversity.

Synthesis and Biological Evaluation of 7‐Alkenyl Homocamptothecins as Potent Topoisomerase I Inhibitors

Wei Guo, Wenfeng Liu, Guoqiang Dong, 2012, Chemistry & biodiversity.

Topoisomerase I‐Mediated Antiproliferative Activity of 10‐Substituted and 12‐Substituted Homocamptothecins

W. Guo, Wenfeng Liu, Yongqiang Zhang, 2011 .

Synthesis and biological evaluation of novel 7-acyl homocamptothecins as Topoisomerase I inhibitors.

Shengzheng Wang, Wei Guo, Wenfeng Liu, 2011, European journal of medicinal chemistry.

Phosphate ester derivatives of homocamptothecin: synthesis, solution stabilities and antitumor activities.

Juan Wang, Wei Guo, Wenfeng Liu, 2010, Bioorganic & medicinal chemistry.

Discovery, synthesis, and biological evaluation of orally active pyrrolidone derivatives as novel inhibitors of p53-MDM2 protein-protein interaction.

Guoqiang Dong, Shengzheng Wang, Zhenyuan Miao, 2012, Journal of medicinal chemistry.

State-of-the-art strategies for targeting protein-protein interactions by small-molecule inhibitors.

Guoqiang Dong, Wei Wang, Wannian Zhang, 2015, Chemical Society reviews.

A Fluorescent Probe for Imaging p53–MDM2 Protein–Protein Interaction

Minyong Li, Zhenyuan Miao, C. Sheng, 2015, Chemical biology & drug design.

Discovery of 7‐Methyl‐10‐Hydroxyhomocamptothecins with 1,2,3‐Triazole Moiety as Potent Topoisomerase I Inhibitors

Wenfeng Liu, Guoqiang Dong, Zhenyuan Miao, 2016, Chemical biology & drug design.

Discovery of 1-arylpyrrolidone derivatives as potent p53-MDM2 inhibitors based on molecule fusing strategy.

Shiping Zhu, Shengzheng Wang, Shanchao Wu, 2014, Bioorganic & medicinal chemistry letters.

3D-QSAR and molecular docking studies on benzothiazole derivatives as Candida albicans N-myristoyltransferase inhibitors.

M. Zhang, Yunlong Song, Zhenyuan Miao, 2007, European journal of medicinal chemistry.

Synthesis and biological evaluation of thio-benzodiazepines as novel small molecule inhibitors of the p53-MDM2 protein-protein interaction.

Guoqiang Dong, Shengzheng Wang, Yang Liu, 2011, European journal of medicinal chemistry.

Homology modeling and molecular dynamics simulation of N-myristoyltransferase from protozoan parasites: active site characterization and insights into rational inhibitor design

Wei Guo, Wenya Wang, Guoqiang Dong, 2009, J. Comput. Aided Mol. Des..

An Indole-Chalcone Inhibits Multidrug-Resistant Cancer Cell Growth by Targeting Microtubules.

Y. Sham, D. Odde, John K. Lee, 2018, Molecular pharmaceutics.

Radiosensitization of human pancreatic cancer by piperlongumine analogues

Zhenyuan Miao, Wannian Zhang, Huojun Zhang, 2020 .

Design, synthesis and biological evaluation of novel 31-hexyloxy chlorin e6-based 152- or 131-amino acid derivatives as potent photosensitizers for photodynamic therapy.

Zhenyuan Miao, Jianzhong Yao, Wannian Zhang, 2020, European journal of medicinal chemistry.

Design, synthesis and structure–activity relationship of 4,5-dihydropyrrolo[3,4-c]pyrazol-6(1H)-ones as potent p53-MDM2 inhibitors

Weihong Zhou, Guoqiang Dong, Zhenyuan Miao, 2017 .

Optical evodiamine derivatives: Asymmetric synthesis and antitumor activity

Shengzheng Wang, Guoqiang Dong, Zhenyuan Miao, 2015 .

Fragment‐growing guided design of Keap1‐Nrf2 protein‐protein interaction inhibitors for targeting myocarditis

H. Zhang, N. Meng, Hua Tang, 2018, Free radical biology & medicine.

Application of a fluorine strategy in the lead optimization of betulinic acid to the discovery of potent CD73 inhibitors

Zhenyuan Miao, Ying Wang, W. Tang, 2022, Steroids.

Discovery and optimization of betulinic acid derivatives as novel potent CD73 inhibitors.

Zhenyuan Miao, Huojun Zhang, Yuelin Wu, 2022, Bioorganic & medicinal chemistry.

Design, synthesis and biological evaluation of novel antitumor spirotetrahydrothiopyran-oxindole derivatives as potent p53-MDM2 inhibitors.

Shengzheng Wang, Jian Li, Zhenyuan Miao, 2017, Bioorganic & medicinal chemistry.

Evolutionary trace analysis of CYP51 family: implication for site-directed mutagenesis and novel antifungal drug design

Shuanghong Chen, Haitao Ji, Wei Guo, 2010, Journal of molecular modeling.

Fragment-Based Discovery of Azocyclic Alkyl Naphthalenesulfonamides as Keap1-Nrf2 Inhibitors for Acute Lung Injury Treatment.

Zhenyuan Miao, Li Ding, Cheng-Shi Jiang, 2023, Journal of medicinal chemistry.

Discovery of Natural Product Ellagic Acid as a Potent CD73 and CD39 Dual Inhibitor.

Zhenyuan Miao, Jianzhong Yao, Yuan Wang, 2020, Bioorganic & medicinal chemistry letters.

Updated research and applications of small molecule inhibitors of Keap1-Nrf2 protein-protein interaction: a review.

Zhenyuan Miao, Wannian Zhang, C. Sheng, 2014, Current medicinal chemistry.

A new strategy to improve the metabolic stability of lactone: discovery of (20S,21S)-21-fluorocamptothecins as novel, hydrolytically stable topoisomerase I inhibitors.

Shiping Zhu, Shengzheng Wang, Jian Li, 2013, Journal of medicinal chemistry.

New azoles with potent antifungal activity: design, synthesis and molecular docking.

Haitao Ji, Yongbing Cao, Guoqiang Dong, 2009, European journal of medicinal chemistry.

Structure-activity relationship and antitumor activity of thio-benzodiazepines as p53-MDM2 protein-protein interaction inhibitors.

Shengzheng Wang, Yongqiang Zhang, Guoqiang Dong, 2012, European journal of medicinal chemistry.

Novel chlorin e6-based conjugates of tyrosine kinase inhibitors: Synthesis and photobiological evaluation as potent photosensitizers for photodynamic therapy.

Y. Li, Zhenyuan Miao, Xingjie Zhang, 2023, European journal of medicinal chemistry.

Novel carboline derivatives as potent antifungal lead compounds: design, synthesis, and biological evaluation.

Shengzheng Wang, Jian Li, Yongqiang Zhang, 2014, ACS Medicinal Chemistry Letters.

Asymmetric Aldol Reactions of Heterocyclic Dienolsilanes and α,β-Unsaturated Carbonyl Derived Dienolsilanes

Zhenyuan Miao, Fen‐er Chen, 2012, Synthesis.

Synthesis and antitumor activity of novel 10-amino acids ester homocamptothecin analogues

W. Guo, Zhenyuan Miao, Wannian Zhang, 2008 .

Antitumor Activities and Structure–Activity Relationship of Phosphotriester Derivatives of Homocamptothecin Based on a Semisynthetic Route

Juan Wang, Shengzheng Wang, Yongqiang Zhang, 2011 .