Zhu‐Jun Yao

2.3k total citations
94 papers, 2.0k citations indexed

About

Zhu‐Jun Yao is a scholar working on Organic Chemistry, Molecular Biology and Biochemistry. According to data from OpenAlex, Zhu‐Jun Yao has authored 94 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 67 papers in Organic Chemistry, 43 papers in Molecular Biology and 28 papers in Biochemistry. Recurrent topics in Zhu‐Jun Yao's work include Traditional and Medicinal Uses of Annonaceae (27 papers), Carbohydrate Chemistry and Synthesis (25 papers) and Synthetic Organic Chemistry Methods (23 papers). Zhu‐Jun Yao is often cited by papers focused on Traditional and Medicinal Uses of Annonaceae (27 papers), Carbohydrate Chemistry and Synthesis (25 papers) and Synthetic Organic Chemistry Methods (23 papers). Zhu‐Jun Yao collaborates with scholars based in China and United States. Zhu‐Jun Yao's co-authors include Yu‐Lin Wu, Xin Cong, Wanguo Wei, Shaozhong Wang, Wen‐Jian Qian, Haibin Zhou, Yu‐Lin Wu, Taishan Hu, Yulin Wu and Yikang Wu and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and PLoS ONE.

In The Last Decade

Zhu‐Jun Yao

94 papers receiving 1.9k citations

Peers

Countries citing papers authored by Zhu‐Jun Yao

Since Specialization

Citations

This map shows the geographic impact of Zhu‐Jun Yao's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Zhu‐Jun Yao with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Zhu‐Jun Yao more than expected).

Fields of papers citing papers by Zhu‐Jun Yao

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Zhu‐Jun Yao. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Zhu‐Jun Yao. The network helps show where Zhu‐Jun Yao may publish in the future.

Co-authorship network of co-authors of Zhu‐Jun Yao

This figure shows the co-authorship network connecting the top 25 collaborators of Zhu‐Jun Yao. A scholar is included among the top collaborators of Zhu‐Jun Yao based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Zhu‐Jun Yao. Zhu‐Jun Yao is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Scalable Cu(II)-mediated intramolecular dehydrogenative phenol-phenol coupling: Concise synthesis of enantiopure axially chiral homo- and hetero-diphenols 2020 ·Chinese Chemical Letters ·(unknown), Tianyang Wang, Ming Gao, Zhu‐Jun Yao	6
2	A gram-scale laboratory synthesis of Annonaceous acetogenin mimic AA005 2020 ·Chinese Chemical Letters ·(unknown), Zhu‐Jun Yao	4
3	Annonaceous acetogenin mimic AA005 suppresses human colon cancer cell growth in vivo through downregulation of Mcl-1 2018 ·Acta Pharmacologica Sinica ·Bing Han, Yuxia Cao, Zhanming Li, Zhaoxia Wu, Yuqin Mao, Hui‐Ling Chen, Zhu‐Jun Yao, Li‐Shun Wang	9
4	Aerobic α-hydroxylation of β-keto esters and amides by co-catalysis of SmI3 and I2 under mild base-free conditions 2016 ·Tetrahedron Letters ·(unknown), Kai Cui, (unknown), Zhen‐Yu Yang, Zhu‐Jun Yao	16
5	Total synthesis of proposed structure of coibamide A, a highly N- and O-methylated cytotoxic marine cyclodepsipeptide 2014 ·Tetrahedron Letters ·Wei He, Haibo Qiu, Yijie Chen, Jie Xi, Zhu‐Jun Yao	18
6	Stereodivergent total synthesis of chlorofusin and its all seven chromophore diastereomers 2014 ·Tetrahedron ·Haibo Qiu, Wen‐Jian Qian, (unknown), Zhu‐Jun Yao	15
7	Unified flexible total synthesis of chlorofusin and artificial Click mimics as antagonists against p53–HDM2 interactions 2014 ·Tetrahedron Letters ·Haibo Qiu, (unknown), Qing Li, Wen‐Jian Qian, (unknown), Gong‐Li Tang, Zhu‐Jun Yao	8
8	Highly Enantioselective Michael Addition of 2‐Oxindole‐ 3‐carboxylate Esters to Nitroolefins Promoted by Cinchona Alkaloid‐Thiourea‐Brønsted Acid Cocatalysts 2012 ·Advanced Synthesis & Catalysis ·Xianjie Chen, Wei Zhu, (unknown), Enguang Feng, Yu Zhou, Jinfang Wang, Hualiang Jiang, Zhu‐Jun Yao, Hong Liu	37
9	Enantioselective Total Synthesis of Marine Diterpenoid Clavulactone 2012 ·Angewandte Chemie International Edition ·Zhen‐Yu Yang, Hongze Liao, (unknown), (unknown), Zhu‐Jun Yao	9
10	Identification of an Annonaceous Acetogenin Mimetic, AA005, as an AMPK Activator and Autophagy Inducer in Colon Cancer Cells 2012 ·PLoS ONE ·Yongqiang Liu, Xin Cheng, (unknown), (unknown), Yijie Chen, Haixia Liu, Qicai Xiao, Sheng Jiang, Zhu‐Jun Yao, Guang‐Biao Zhou	34
11	Development of novel conformation-constrained cytotoxic derivatives of cheliensisin A by embedment of small heterocycles 2011 ·European Journal of Medicinal Chemistry ·Xu Deng, Jia Su, Yu Zhao, Li‐Yan Peng, Yan Li, Zhu‐Jun Yao, Qin‐Shi Zhao	12
12	Three‐Component Reactions of Isochromenylium Tetrafluoroborates via Non‐Classical [4+2]‐Intermediates: Mild One‐Step Metal‐Free Synthesis of Functionalized Dihydronaphthalenes and Tetrahydronaphthalenes 2010 ·Chemistry - A European Journal ·(unknown), Zhen‐Yu Yang, Shaozhong Wang, Zhu‐Jun Yao	19
13	Azaanthraquinone assembly from N-propargylamino quinone via iodine-induced 6-endo-dig electrophilic cyclization 2010 ·Organic & Biomolecular Chemistry ·(unknown), (unknown), Shaozhong Wang, Hua‐Qin Wang, Zhu‐Jun Yao	35
14	Novel sinomenine derivative 1032 improves immune suppression in experimental autoimmune encephalomyelitis 2009 ·Biochemical and Biophysical Research Communications ·(unknown), Enguang Bi, (unknown), Xiaodong Wu, (unknown), (unknown), Yuan Wang, (unknown), Guomei Lin, Shuhui Sun, Chao Bian, Aizhong Chen, Zhu‐Jun Yao, Bing Sun	19
15	Annonaceous acetogenin mimics bearing a terminal lactam and their cytotoxicity against cancer cells 2007 ·Bioorganic & Medicinal Chemistry Letters ·Haixia Liu, Guorui Huang, (unknown), Jiarui Wu, Zhu‐Jun Yao	23
16	Effects of Generated <i>trans</i>-Arachidonic Acids on Retinal Capillary during Nitrative Stress in Diabetic Rats 2007 ·Ophthalmologica ·Lin Xu, (unknown), Zhu‐Jun Yao, Yumin Liu, Yunping Qiu, Kun Liu, Dongqing Zhu, Qing Gu, Xun Xu, Patrick Ho	5
17	A Structure–Activity Guided Strategy for Fluorescent Labeling of Annonaceous Acetogenin Mimetics and their Application in Cell Biology 2006 ·ChemBioChem ·Haixia Liu, Guorui Huang, (unknown), Sheng Jiang, Jiarui Wu, Zhu‐Jun Yao	34
18	Induction of Cell Death of Gastric Cancer Cells by a Modified Compound of the Annonaceous Acetogenin Family 2003 ·ChemBioChem ·Guorui Huang, Sheng Jiang, Yu‐Lin Wu, Yan Jin, Zhu‐Jun Yao, Jiarui Wu	28
19	A straightforward synthesis of DAH (3-deoxy-D-arabino-hept-2-ulosonic acid) and DRH (3-deoxy-D-ribo-hept-2-ulosonic acid) 2002 ·Journal of the Chemical Society Perkin Transactions 1 ·(unknown), (unknown), Yikang Wu, (unknown), Zhu‐Jun Yao, Yulin Wu	5
20	Studies on Mimicry of Naturally Occurring Annonaceous Acetogenins: Non‐THF Analogues Leading to Remarkable Selective Cytotoxicity against Human Tumor Cells 2002 ·Chemistry - A European Journal ·Bu‐Bing Zeng, Yikang Wu, Sheng Jiang, Yu Qian, Zhu‐Jun Yao, (unknown), Hongyan Li, Yan Li, Xiaoguang Chen, Yu‐Lin Wu	36

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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