Sergey A. Kozmin

5.6k total citations · 1 hit paper
70 papers, 4.6k citations indexed

About

Sergey A. Kozmin is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, Sergey A. Kozmin has authored 70 papers receiving a total of 4.6k indexed citations (citations by other indexed papers that have themselves been cited), including 55 papers in Organic Chemistry, 25 papers in Molecular Biology and 10 papers in Pharmacology. Recurrent topics in Sergey A. Kozmin's work include Synthetic Organic Chemistry Methods (39 papers), Chemical Synthesis and Analysis (16 papers) and Catalytic Alkyne Reactions (16 papers). Sergey A. Kozmin is often cited by papers focused on Synthetic Organic Chemistry Methods (39 papers), Chemical Synthesis and Analysis (16 papers) and Catalytic Alkyne Reactions (16 papers). Sergey A. Kozmin collaborates with scholars based in United States and Russia. Sergey A. Kozmin's co-authors include Liming Zhang, Jianwei Sun, Viresh H. Rawal, Tetsuo Iwama, Amos B. Smith, Michael P. Schramm, Christopher M. Adams, Yong Huang, Jiayue Cui and Daniel V. Paone and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Angewandte Chemie International Edition.

In The Last Decade

Sergey A. Kozmin

70 papers receiving 4.6k citations

Hit Papers

Gold and Platinum Catalysis of Enyne Cycloisomerization 2006 2026 2012 2019 2006 250 500 750

Peers

Sergey A. Kozmin
Paul Helquist United States
Scott E. Schaus United States
Janice M. Klunder United States
Philip Kocieński United Kingdom
Jeffrey N. Johnston United States
Paul Helquist United States
Sergey A. Kozmin
Citations per year, relative to Sergey A. Kozmin Sergey A. Kozmin (= 1×) peers Paul Helquist

Countries citing papers authored by Sergey A. Kozmin

Since Specialization
Citations

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

Fields of papers citing papers by Sergey A. Kozmin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sergey A. Kozmin. 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 Sergey A. Kozmin. The network helps show where Sergey A. Kozmin may publish in the future.

Co-authorship network of co-authors of Sergey A. Kozmin

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

All Works

20 of 20 papers shown
1.
Efimova, Elena V., Satoe Takahashi, Ding Wu, et al.. (2015). Linking Cancer Metabolism to DNA Repair and Accelerated Senescence. Molecular Cancer Research. 14(2). 173–184. 42 indexed citations
2.
Türkmen, Yunus E., et al.. (2013). [2+2+2] Cycloadditions of Siloxy Alkynes with 1,2‐Diazines: From Reaction Discovery to Identification of an Antiglycolytic Chemotype. Angewandte Chemie International Edition. 52(51). 13576–13579. 24 indexed citations
3.
Türkmen, Yunus E., et al.. (2013). [2+2+2] Cycloadditions of Siloxy Alkynes with 1,2‐Diazines: From Reaction Discovery to Identification of an Antiglycolytic Chemotype. Angewandte Chemie. 125(51). 13821–13824. 7 indexed citations
4.
Cabrera‐Pardo, Jaime R., David Chai, Song Liu, Milan Mrksich, & Sergey A. Kozmin. (2013). Label-assisted mass spectrometry for the acceleration of reaction discovery and optimization. Nature Chemistry. 5(5). 423–427. 89 indexed citations
5.
Cabrera‐Pardo, Jaime R., David Chai, & Sergey A. Kozmin. (2013). Silver‐Promoted Benzannulations of Siloxyalkynes with Pyridinium and Isoquinolinium Salts. Advanced Synthesis & Catalysis. 355(13). 2495–2498. 22 indexed citations
6.
Liu, Song, John S. Scotti, & Sergey A. Kozmin. (2013). Emulating the Logic of Monoterpenoid Alkaloid Biogenesis to Access a Skeletally Diverse Chemical Library. The Journal of Organic Chemistry. 78(17). 8645–8654. 39 indexed citations
7.
Türkmen, Yunus E., et al.. (2012). Silver-Catalyzed Formal Inverse Electron-Demand Diels–Alder Reaction of 1,2-Diazines and Siloxy Alkynes. Journal of the American Chemical Society. 134(22). 9062–9065. 63 indexed citations
8.
Li, Jing, et al.. (2011). Three-component reaction discovery enabled by mass spectrometry of self-assembled monolayers. Nature Chemistry. 4(1). 45–51. 45 indexed citations
9.
Pronin, Sergey V., Anthony Martinez, Konstantin Kuznedelov, et al.. (2011). Chemical Synthesis Enables Biochemical and Antibacterial Evaluation of Streptolydigin Antibiotics. Journal of the American Chemical Society. 133(31). 12172–12184. 39 indexed citations
10.
Ulanovskaya, Olesya A., Jiayue Cui, Stephen J. Kron, & Sergey A. Kozmin. (2011). A Pairwise Chemical Genetic Screen Identifies New Inhibitors of Glucose Transport. Chemistry & Biology. 18(2). 222–230. 38 indexed citations
11.
Cui, Jiayue, et al.. (2010). Synthesis of a High‐Purity Chemical Library Reveals a Potent Inducer of Oxidative Stress. ChemBioChem. 11(9). 1224–1227. 3 indexed citations
12.
Rizvi, Abrar, Jiayue Cui, Colleen T. Skau, et al.. (2009). Identification and Characterization of a Small Molecule Inhibitor of Formin-Mediated Actin Assembly. Chemistry & Biology. 16(11). 1158–1168. 273 indexed citations
13.
Ulanovskaya, Olesya A., Jelena M. Janjic, Masato Suzuki, et al.. (2008). Synthesis enables identification of the cellular target of leucascandrolide A and neopeltolide. Nature Chemical Biology. 4(7). 418–424. 82 indexed citations
14.
Marjanovic, Jasmina & Sergey A. Kozmin. (2007). Spirofungin A: Stereoselective Synthesis and Inhibition of Isoleucyl‐tRNA Synthetase. Angewandte Chemie International Edition. 46(46). 8854–8857. 46 indexed citations
15.
Sun, Jianwei & Sergey A. Kozmin. (2006). Silver‐Catalyzed Hydroamination of Siloxy Alkynes. Angewandte Chemie International Edition. 45(30). 4991–4993. 68 indexed citations
16.
Wang, Ying, Jelena M. Janjic, & Sergey A. Kozmin. (2005). Synthesis of leucascandrolide A. Pure and Applied Chemistry. 77(7). 1161–1169. 22 indexed citations
17.
Bai, Ruoli, Jeremy L. Baryza, Vishal Verma, et al.. (2005). Actin is the primary cellular receptor of bistramide A. Nature Chemical Biology. 1(7). 383–388. 67 indexed citations
18.
Kozmin, Sergey A. & Ying Wang. (2003). A Three‐Dimensional Array for Multiparallel Synthesis. Angewandte Chemie International Edition. 42(8). 903–905. 14 indexed citations
19.
Liu, Dong & Sergey A. Kozmin. (2001). Catalytic Enantioselective Isomerization of Silacyclopentene Oxides: New Strategy for Stereocontrolled Assembly of Acyclic Polyols. Angewandte Chemie International Edition. 40(24). 4757–4759. 36 indexed citations
20.
Kozmin, Sergey A. & Viresh H. Rawal. (1997). Preparation and Diels−Alder Reactivity of 1-Amino-3-siloxy-1,3-butadienes. The Journal of Organic Chemistry. 62(16). 5252–5253. 105 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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