Tu‐Hsin Yan

1.1k citations

46 papers · 764 · h-index 17

Impact in

Organic Chemistry top 5%
- Asymmetric Synthesis and Catalysis
- Synthetic Organic Chemistry Methods
- Chemical synthesis and alkaloids
- Catalytic C–H Functionalization Methods
- Cyclopropane Reaction Mechanisms
- Synthesis and Catalytic Reactions
- Carbohydrate Chemistry and Synthesis
Pharmaceutical Science top 5%

Papers in

Organic Chemistry 44
- Asymmetric Synthesis and Catalysis 22
- Synthetic Organic Chemistry Methods 11
- Chemical synthesis and alkaloids 8
- Cyclopropane Reaction Mechanisms 8
- Advanced Synthetic Organic Chemistry 8
- Synthesis and Catalytic Reactions 8
Molecular Biology 9
- Chemical Synthesis and Analysis 8

Co-authors: Ying-Chuan Wang (13 shared papers)Kuo‐Wei Lin (7 shared papers)H. Christine Lo (5 shared papers)Ching‐Ting Chien (4 shared papers)Hui‐Chun Lee (4 shared papers)Pei‐Chen Huang (1 shared paper)Leo A. Paquette (2 shared papers)Keith A. Horn (2 shared papers)
Journals: The Journal of Organic Chemistry (12 papers)Organic Letters (9 papers)Tetrahedron Letters (7 papers)Tetrahedron (4 papers)Tetrahedron Asymmetry (3 papers)
Partner nations: Taiwan United States

In The Last Decade

Tu‐Hsin Yan

46 papers receiving 738 citations

Peers

Countries citing papers authored by Tu‐Hsin Yan

Since Specialization

Citations

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

Fields of papers citing papers by Tu‐Hsin Yan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tu‐Hsin Yan. 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 Tu‐Hsin Yan. The network helps show where Tu‐Hsin Yan may publish in the future.

Co-authors

The 10 scholars most cited alongside Tu‐Hsin Yan, 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 Tu‐Hsin Yan Line = papers co-authored together Tu‐Hsin Yan 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 46 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Dichloromethane Activation. Direct Methylenation of Ketones and Aldehydes with CH₂Cl₂ Promoted by Mg/TiCl₄/THF Organic Letters ·Tu‐Hsin Yan, Chia‐Chung Tsai, Ching‐Ting Chien, Chia‐Ching Cho, Pei‐Chen Huang	2004	73
2	A Short Synthesis of (+)-Narciclasine via a Strategy Derived from Stereocontrolled Epoxide Formation and SnCl₄-Catalyzed Arene-Epoxide Coupling The Journal of Organic Chemistry ·Shanmugham Elango, Tu‐Hsin Yan	2002	55
3	A Flexible Strategy Based on a C₂-Symmetric Pool of Chiral Substrates: Concise Synthesis of (+)-Valienamine, Key Intermediate of (+)- Pancratistatin, and Conduramines A-1 and E Organic Letters ·Yuan‐Kang Chang, H. Christine Lo, Tu‐Hsin Yan	2009	40
4	Asymmetric Aldol Type Reactions of Acetate Imide Enolates The Journal of Organic Chemistry ·Tu‐Hsin Yan, An‐Wei Hung, Hui‐Chun Lee, Chii‐Shin Chang, Wen‐Hung Liu	1995	39
5	A short synthesis of (+)-lycoricidine Tetrahedron ·Shanmugham Elango, Tu‐Hsin Yan	2002	35
6	New, General, and Practical Enamine Cyclopropanation Using Dichloromethane Organic Letters ·Chia‐Chung Tsai, I‐Lin Hsieh, Tsung‐Ting Cheng, Ping‐Kuei Tsai, Kuo‐Wei Lin, Tu‐Hsin Yan	2006	29
7	A novel DMAP-promoted oxazolidinethione deacylation. Application for the direct conversion of the initial chiral thioimide aldols to various ester protecting groups Tetrahedron Letters ·Dah‐Wei Su, Ying-Chuan Wang, Tu‐Hsin Yan	1999	28
8	Silicon in organic synthesis—17 Tetrahedron ·Leo A. Paquette, Gregory J. Wells, Keith A. Horn, Tu‐Hsin Yan	1983	28
9	Exceedingly Concise and Elegant Synthesis of (+)-Paniculatine, (−)-Magellanine, and (+)-Magellaninone Organic Letters ·Kuo‐Wei Lin, Bakthavachalam Ananthan, Sheng-Fang Tseng, Tu‐Hsin Yan	2015	27
10	Dichloromethane as an Unusual Methylene Equivalent. A New Entry of Highly Nucleophilic and Selective Titanium−Methylene Complexes for Ester Methylenation Organic Letters ·Tu‐Hsin Yan, Ching‐Ting Chien, Chia‐Chung Tsai, Kuo‐Wei Lin, Yen‐Hsien Wu	2004	26
11	A General, Highly Anti-Stereoselective Aldolization Method via Camphor-Derived Boryl Enolates The Journal of Organic Chemistry ·Ying-Chuan Wang, An‐Wei Hung, Chii‐Shin Chang, Tu‐Hsin Yan	1996	21
12	Silicon in organic synthesis. 14. Five ring annulation processes based upon thermal rearrangement of (1-trimethylsilylcyclopropyl)ethylenes Tetrahedron Letters ·Leo A. Paquette, Gregory J. Wells, Keith A. Horn, Tu‐Hsin Yan	1982	20
13	An Unusual Enantioselective Aldol-Type Reaction of an Acetate Boryl Enolate Derived from a Chiral Thioimide The Journal of Organic Chemistry ·Tu‐Hsin Yan, An‐Wei Hung, Hui‐Chun Lee, Chii‐Shin Chang	1994	19
14	Novel Asymmetric Route to Carbanucleoside and Prostanoid Intermediates: Efficient Preparation of Both Optical Antipodes of Chiral Cyclopentenone The Journal of Organic Chemistry ·C. H. Lin, Ying-Chuan Wang, Jung-Lang Hsu, Chao‐Cheng Chiang, Dah‐Wei Su, Tu‐Hsin Yan	1997	19
15	New, General, and Practical Preparation of Methyl Ketones via the Direct Coupling of Amides with CH₂Cl₂ Promoted by TiCl₄/Mg Organic Letters ·Kuo‐Wei Lin, Chi‐Hui Tsai, I‐Lin Hsieh, Tu‐Hsin Yan	2008	19
16	Unusual Ambiphilic Carbenoid Equivalent in Amide Cyclopropanation Organic Letters ·Kuo‐Wei Lin, Shiuan Yan, I‐Lin Hsieh, Tu‐Hsin Yan	2006	17
17	Toward the Development of a General Chiral α-Substituted Acetate Enolate Synthon for Aldolization. DMAP- and NEt₃-Promoted Oxazolidinethione “Deacylation” The Journal of Organic Chemistry ·Ying-Chuan Wang, Dah‐Wei Su, Chen‐Men Lin, Hsi‐Liang Tseng, Chi‐Lung Li, Tu‐Hsin Yan	1999	17
18	Chiral Pool Based Efficient Synthesis of the Aminocyclitol Core and Furanoside of (−)- Hygromycin A: Formal Total Synthesis of (−)-Hygromycin A Organic Letters ·H. Christine Lo, Yuan‐Kang Chang, Tu‐Hsin Yan	2012	16
19	“Non-Evans” syn aldol via aldolization of chlorotitanium enolate with TiCl4/aldehyde complex Tetrahedron Letters ·Tu‐Hsin Yan, Hui‐Chun Lee, Chang‐Wei Tan	1993	16
20	A C₂-Symmetric Chiral Pool-Based Flexible Strategy: Synthesis of (+)- and (−)-Shikimic Acids, (+)- and (−)-4-epi-Shikimic Acids, and (+)- and (−)-Pinitol The Journal of Organic Chemistry ·Bakthavachalam Ananthan, Wan‐Chun Chang, Jhe‐Sain Lin, Pin-hui Li, Tu‐Hsin Yan	2014	15

About Tu‐Hsin Yan

Tu‐Hsin Yan is a scholar working on Organic Chemistry, Molecular Biology, Spectroscopy, Inorganic Chemistry and Pharmacology, having authored 46 papers that have together received 764 indexed citations. Recurring topics across this work include Asymmetric Synthesis and Catalysis (22 papers), Synthetic Organic Chemistry Methods (11 papers), Molecular spectroscopy and chirality (9 papers), Chemical synthesis and alkaloids (8 papers), Cyclopropane Reaction Mechanisms (8 papers), Chemical Synthesis and Analysis (8 papers), Advanced Synthetic Organic Chemistry (8 papers) and Synthesis and Catalytic Reactions (8 papers). The work is most often cited by research in Organic Chemistry (702 citations), Pharmaceutical Science (63 citations), Pharmacology (78 citations), Inorganic Chemistry (110 citations) and Pharmacology (63 citations). Tu‐Hsin Yan has collaborated with scholars based in Taiwan and United States. Frequent co-authors include Ying-Chuan Wang, Kuo‐Wei Lin, H. Christine Lo, Ching‐Ting Chien, Hui‐Chun Lee, Pei‐Chen Huang, Leo A. Paquette, Keith A. Horn, Gregory J. Wells and Yu‐Cheng Chang. Their work appears in journals such as The Journal of Organic Chemistry, Organic Letters, Tetrahedron Letters, Tetrahedron and Tetrahedron Asymmetry.

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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