David W. Lin

1.6k total citations
8 papers, 1.0k citations indexed

About

David W. Lin is a scholar working on Organic Chemistry, Biotechnology and Pharmacology. According to data from OpenAlex, David W. Lin has authored 8 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Organic Chemistry, 2 papers in Biotechnology and 1 paper in Pharmacology. Recurrent topics in David W. Lin's work include Catalytic C–H Functionalization Methods (3 papers), Cyclopropane Reaction Mechanisms (3 papers) and Asymmetric Synthesis and Catalysis (2 papers). David W. Lin is often cited by papers focused on Catalytic C–H Functionalization Methods (3 papers), Cyclopropane Reaction Mechanisms (3 papers) and Asymmetric Synthesis and Catalysis (2 papers). David W. Lin collaborates with scholars based in United States. David W. Lin's co-authors include Phil S. Baran, Jin‐Quan Yu, Masayuki Wasa, Jeremy M. Richter, Keary M. Engle, Eun Jeong Yoo, Ru‐Yi Zhu, Motofumi Miura, Kai‐Jiong Xiao and Wei Gong and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and The Journal of Organic Chemistry.

In The Last Decade

David W. Lin

8 papers receiving 1.0k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
David W. Lin United States	8	980	268	73	62	44	8	1.0k
Maksim Osipov United States	12	763 0.8×	209 0.8×	79 1.1×	66 1.1×	32 0.7×	13	796
Yasutomo Yamamoto Japan	20	1.1k 1.1×	229 0.9×	103 1.4×	73 1.2×	25 0.6×	59	1.1k
Tomás Llamas Spain	8	733 0.7×	240 0.9×	128 1.8×	60 1.0×	38 0.9×	8	770
Alexander Duschek Germany	11	770 0.8×	137 0.5×	50 0.7×	41 0.7×	22 0.5×	12	789
Hideyuki Tsutsui Japan	15	917 0.9×	165 0.6×	55 0.8×	28 0.5×	23 0.5×	22	967
Alexandria P. Brucks United States	6	554 0.6×	192 0.7×	51 0.7×	39 0.6×	46 1.0×	7	602
Michele Gatti Switzerland	16	1.2k 1.2×	425 1.6×	192 2.6×	42 0.7×	49 1.1×	18	1.3k
Stephen A. Hermitage United Kingdom	16	672 0.7×	227 0.8×	141 1.9×	42 0.7×	28 0.6×	45	729
Xiaotao Pu China	13	620 0.6×	136 0.5×	128 1.8×	32 0.5×	63 1.4×	14	709

Countries citing papers authored by David W. Lin

Since Specialization

Citations

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

Fields of papers citing papers by David W. Lin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David W. Lin

This figure shows the co-authorship network connecting the top 25 collaborators of David W. Lin. A scholar is included among the top collaborators of David W. Lin 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 David W. Lin. David W. Lin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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8 of 8 papers shown

1.

Xiao, Kai‐Jiong, David W. Lin, Motofumi Miura, et al.. (2014). Palladium(II)-Catalyzed Enantioselective C(sp³)–H Activation Using a Chiral Hydroxamic Acid Ligand. Journal of the American Chemical Society. 136(22). 8138–8142. 234 indexed citations

2.

Usui, Ippei, David W. Lin, Takeshi Masuda, & Phil S. Baran. (2013). Convergent Synthesis and Structural Confirmation of Phellodonin and Sarcodonin ε. Organic Letters. 15(9). 2080–2083. 27 indexed citations

3.

Lin, David W., et al.. (2011). Synthesis-Guided Structure Revision of the Sarcodonin, Sarcoviolin, and Hydnellin Natural Product Family. The Journal of Organic Chemistry. 76(4). 1013–1030. 48 indexed citations

4.

Wasa, Masayuki, Keary M. Engle, David W. Lin, Eun Jeong Yoo, & Jin‐Quan Yu. (2011). Pd(II)-Catalyzed Enantioselective C–H Activation of Cyclopropanes. Journal of the American Chemical Society. 133(49). 19598–19601. 354 indexed citations

5.

Richter, Jeremy M., et al.. (2007). Scope and Mechanism of Direct Indole and Pyrrole Couplings Adjacent to Carbonyl Compounds: Total Synthesis of Acremoauxin A and Oxazinin 3. Journal of the American Chemical Society. 129(42). 12857–12869. 161 indexed citations

6.

Baran, Phil S., Narendra B. Ambhaikar, Carlos A. Guerrero, et al.. (2006). Oxidative C–C bond formation in heterocyclic chemistry. ARKIVOC. 2006(7). 310–325. 25 indexed citations

7.

Baran, Phil S., Jeremy M. Richter, & David W. Lin. (2004). Direct Coupling of Pyrroles with Carbonyl Compounds: Short Enantioselective Synthesis of (S)‐Ketorolac. Angewandte Chemie. 117(4). 615–618. 48 indexed citations

8.

Baran, Phil S., Jeremy M. Richter, & David W. Lin. (2004). Direct Coupling of Pyrroles with Carbonyl Compounds: Short Enantioselective Synthesis of (S)‐Ketorolac. Angewandte Chemie International Edition. 44(4). 609–612. 130 indexed citations

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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