Aijun Lin

5.6k citations

149 papers · 4.9k indexed · h-index 44

Impact in

Organic Chemistry top 0.2%
- Catalytic C–H Functionalization Methods
- Asymmetric Synthesis and Catalysis
- Synthesis of Indole Derivatives
- Cyclopropane Reaction Mechanisms
- Sulfur-Based Synthesis Techniques
- Synthesis and Catalytic Reactions
- Catalytic Cross-Coupling Reactions
Pharmaceutical Science top 1%

Papers in ⓘ

Organic Chemistry 140
- Catalytic C–H Functionalization Methods 78
- Asymmetric Synthesis and Catalysis 40
- Cyclopropane Reaction Mechanisms 24
- Synthesis and Catalytic Reactions 24
- Synthesis of Indole Derivatives 22
- Catalytic Cross-Coupling Reactions 22
- Sulfur-Based Synthesis Techniques 19
Inorganic Chemistry 23
- Asymmetric Hydrogenation and Catalysis 22

Co-authors: Hequan Yao (97 shared papers)Zhenbo Yuan (11 shared papers)Yixiang Cheng (22 shared papers)Shang Gao (24 shared papers)Jinyi Xu (28 shared papers)Xinxin Fang (9 shared papers)Jiong Yang (5 shared papers)Xuanyi Li (10 shared papers)
Journals: Organic Letters (42 papers)Organic Chemistry Frontiers (12 papers)Advanced Synthesis & Catalysis (12 papers)Organic & Biomolecular Chemistry (8 papers)Angewandte Chemie International Edition (8 papers)
Partner nations: China United States Japan

In The Last Decade

Aijun Lin

144 papers receiving 4.8k citations

Peers

Countries citing papers authored by Aijun Lin

Since Specialization

Citations

This map shows the geographic impact of Aijun Lin'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 Aijun Lin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Aijun Lin more than expected).

Fields of papers citing papers by Aijun Lin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Aijun Lin. 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 Aijun Lin. The network helps show where Aijun Lin may publish in the future.

Co-authors

The 25 scholars most cited alongside Aijun Lin, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Aijun Lin Line = papers co-authored together Aijun Lin links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 149 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Organocatalyzed Asymmetric 1,6-Conjugate Addition of para-Quinone Methides with Dicyanoolefins Organic Letters ·Xuanyi Li, Xiuyan Xu, Weiwei Wei, Aijun Lin, Hequan Yao	2016	135
2	Bifunctional Organo/Metal Cooperatively Catalyzed [3 + 2] Annulation of para-Quinone Methides with Vinylcyclopropanes: Approach to Spiro[4.5]deca-6,9-diene-8-ones Organic Letters ·Zhenbo Yuan, Weiwei Wei, Aijun Lin, Hequan Yao	2016	134
3	1,6-Conjugated Addition-Mediated [2+1] Annulation: Approach to Spiro[2.5]octa-4,7-dien-6-one The Journal of Organic Chemistry ·Zhenbo Yuan, Xinxin Fang, Xuanyi Li, Jie Wu, Hequan Yao, Aijun Lin	2015	125
4	Synthesis of spiro[2.5]octa-4,7-dien-6-one with consecutive quaternary centers via 1,6-conjugate addition induced dearomatization of para-quinone methides Chemical Communications ·Kuo Gai, Xinxin Fang, Xuanyi Li, Jinyi Xu, Jinhui Wu, Aijun Lin, Hequan Yao	2015	115
5	Controllable Rh(III)-Catalyzed Annulation between Salicylaldehydes and Diazo Compounds: Divergent Synthesis of Chromones and Benzofurans Organic Letters ·Peng Sun, Shang Gao, Chi Yang, Songjin Guo, Aijun Lin, Hequan Yao	2016	102
6	1,6‐Addition Arylation of para‐Quinone Methides: An Approach to Unsymmetrical Triarylmethanes European Journal of Organic Chemistry ·Shang Gao, Xiuyan Xu, Zhenbo Yuan, Haipin Zhou, Hequan Yao, Aijun Lin	2016	89
7	Rh(III)-Catalyzed Redox-Neutral Annulation of Primary Benzamides with Diazo Compounds: Approach to Isoquinolinones The Journal of Organic Chemistry ·Youzhi Wu, Peng Sun, Kaifan Zhang, Tie Yang, Hequan Yao, Aijun Lin	2016	89
8	1,6-Conjugated addition-mediated [4 + 1] annulation: an approach to 2,3-dihydrobenzofurans Organic Chemistry Frontiers ·Lina Liu, Zhenbo Yuan, Rui Pan, Yuye Zeng, Aijun Lin, Hequan Yao, Yue Huang	2017	85
9	Organocatalytic oxa/aza-Michael–Michael Cascade Strategy for the Construction of Spiro [Chroman/Tetrahydroquinoline-3,3′-oxindole] Scaffolds Organic Letters ·Haibin Mao, Aijun Lin, Yang Tang, Yan Shi, Hongwen Hu, Yixiang Cheng, Chengjian Zhu	2013	83
10	[3 + 3] Cycloaddition of in Situ Formed Azaoxyallyl Cations with 2-Alkenylindoles: An Approach to Tetrahydro-β-carbolinones Organic Letters ·Kaifan Zhang, Xiao‐Ying Xu, Jiuan Zheng, Hequan Yao, Yue Huang, Aijun Lin	2017	78
11	Recent advances in C–H fluorination Organic Chemistry Frontiers ·Aijun Lin, C. Bryan Huehls, Jiong Yang	2014	78
12	Solvent-Controlled Switchable C–H Alkenylation of 4-Aryl-1H-pyrrole-3-carboxylates: Application to the Total Synthesis of (±)-Rhazinilam Organic Letters ·Youla Su, Haipin Zhou, Jiaxuan Chen, Jinyi Xu, Jinhui Wu, Aijun Lin, Hequan Yao	2014	75
13	Cascade Radical 1,6-Addition/Cyclization ofpara-Quinone Methides: Leading to Spiro[4.5]deca-6,9-dien-8-ones Organic Letters ·Rui Pan, Lingyin Hu, Chunhua Han, Aijun Lin, Hequan Yao	2018	72
14	N-Indolyltriethylborate: A Useful Reagent for Synthesis of C3-Quaternary Indolenines Organic Letters ·Aijun Lin, Jiong Yang, Mohamed Hashim	2013	71
15	Palladium-catalyzed allylic alkylation dearomatization of β-naphthols and indoles withgem-difluorinated cyclopropanes Chemical Communications ·Zhiyuan Fu, Jianping Zhu, Songjin Guo, Aijun Lin	2020	71
16	Multiple Roles of the Pyrimidyl Group in the Rhodium‐Catalyzed Regioselective Synthesis and Functionalization of Indole‐3‐carboxylic Acid Esters Advanced Synthesis & Catalysis ·Hui Jiang, Shang Gao, Jinyi Xu, Jinhui Wu, Aijun Lin, Hequan Yao	2016	69
17	Palladium‐Catalyzed Asymmetric Intramolecular Reductive Heck Desymmetrization of Cyclopentenes: Access to Chiral Bicyclo[3.2.1]octanes Angewandte Chemie International Edition ·Zhenbo Yuan, Ziwen Feng, Yuye Zeng, Xiaobin Zhao, Aijun Lin, Hequan Yao	2019	68
18	[3 + 2] Cycloaddition Reaction of in Situ Formed Azaoxyallyl Cations with Aldehydes: An Approach to Oxazolidin-4-ones Organic Letters ·Kaifan Zhang, Chi Yang, Hequan Yao, Aijun Lin	2016	68
19	Constructing chiral bicyclo[3.2.1]octanes via palladium-catalyzed asymmetric tandem Heck/carbonylation desymmetrization of cyclopentenes Nature Communications ·Zhenbo Yuan, Yuye Zeng, Ziwen Feng, Zhe Guan, Aijun Lin, Hequan Yao	2020	66
20	Ligand-Controlled, Palladium-Catalyzed Asymmetric [4+4] and [2+4] Cycloadditions Organic Letters ·Qiuyu Li, Rui Pan, Meihui Wang, Hequan Yao, Aijun Lin	2021	64

About Aijun Lin

Aijun Lin is a scholar working on Organic Chemistry, Inorganic Chemistry, Pharmaceutical Science, Toxicology and Pharmacology, having authored 149 papers that have together received 4.9k indexed citations. Recurring topics across this work include Catalytic C–H Functionalization Methods (78 papers), Asymmetric Synthesis and Catalysis (40 papers), Cyclopropane Reaction Mechanisms (24 papers), Synthesis and Catalytic Reactions (24 papers), Synthesis of Indole Derivatives (22 papers), Catalytic Cross-Coupling Reactions (22 papers), Asymmetric Hydrogenation and Catalysis (22 papers) and Sulfur-Based Synthesis Techniques (19 papers). The work is most often cited by research in Organic Chemistry (4.6k citations), Pharmaceutical Science (328 citations), Toxicology (165 citations), Inorganic Chemistry (604 citations) and Process Chemistry and Technology (39 citations). Aijun Lin has collaborated with scholars based in China, United States and Japan. Frequent co-authors include Hequan Yao, Zhenbo Yuan, Yixiang Cheng, Shang Gao, Jinyi Xu, Xinxin Fang, Jiong Yang, Xuanyi Li, Chengjian Zhu and Rui Pan. Their work appears in journals such as Organic Letters, Organic Chemistry Frontiers, Advanced Synthesis & Catalysis, Organic & Biomolecular Chemistry and Angewandte Chemie International Edition.

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