Barbara Zajc

1.4k total citations
59 papers, 1.0k citations indexed

About

Barbara Zajc is a scholar working on Organic Chemistry, Pharmaceutical Science and Molecular Biology. According to data from OpenAlex, Barbara Zajc has authored 59 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Organic Chemistry, 28 papers in Pharmaceutical Science and 11 papers in Molecular Biology. Recurrent topics in Barbara Zajc's work include Fluorine in Organic Chemistry (28 papers), DNA and Nucleic Acid Chemistry (10 papers) and Sulfur-Based Synthesis Techniques (8 papers). Barbara Zajc is often cited by papers focused on Fluorine in Organic Chemistry (28 papers), DNA and Nucleic Acid Chemistry (10 papers) and Sulfur-Based Synthesis Techniques (8 papers). Barbara Zajc collaborates with scholars based in United States, Slovenia and Netherlands. Barbara Zajc's co-authors include Arun K. Ghosh, Rakesh Kumar, Marko Zupan, Mahesh K. Lakshman, Jane M. Sayer, Donald M. Jerina, Padmanava Pradhan, Shaibal Banerjee, Samir Mandal and Anthony Dipple and has published in prestigious journals such as Journal of the American Chemical Society, Journal of Biological Chemistry and Biochemistry.

In The Last Decade

Barbara Zajc

58 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Barbara Zajc United States 20 686 476 311 159 74 59 1.0k
Sergey V. Ryabukhin Ukraine 24 1.5k 2.2× 359 0.8× 415 1.3× 196 1.2× 53 0.7× 146 1.8k
Guido Verniest Belgium 22 1.0k 1.5× 350 0.7× 237 0.8× 116 0.7× 17 0.2× 70 1.2k
F. L. MERCHAN Spain 25 1.5k 2.2× 157 0.3× 706 2.3× 127 0.8× 47 0.6× 106 1.6k
Christophe Hoarau France 27 1.9k 2.7× 190 0.4× 255 0.8× 182 1.1× 20 0.3× 75 2.2k
Daniel Zimmerli Switzerland 10 580 0.8× 474 1.0× 275 0.9× 146 0.9× 11 0.1× 17 883
Joseph F. Dellaria United States 18 1.1k 1.6× 113 0.2× 561 1.8× 165 1.0× 54 0.7× 26 1.4k
Philip B. Cox United States 16 709 1.0× 105 0.2× 468 1.5× 103 0.6× 19 0.3× 22 1.2k
Maria Cristina Bellucci Italy 18 700 1.0× 99 0.2× 517 1.7× 96 0.6× 38 0.5× 50 1.1k
Ignatius J. Turchi United States 17 1.5k 2.1× 108 0.2× 484 1.6× 107 0.7× 113 1.5× 39 1.8k
Fiorenza Viani Italy 21 974 1.4× 604 1.3× 507 1.6× 153 1.0× 10 0.1× 96 1.3k

Countries citing papers authored by Barbara Zajc

Since Specialization
Citations

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

Fields of papers citing papers by Barbara Zajc

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Barbara Zajc

This figure shows the co-authorship network connecting the top 25 collaborators of Barbara Zajc. A scholar is included among the top collaborators of Barbara Zajc 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 Barbara Zajc. Barbara Zajc 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.
Bae, Suyeal, et al.. (2022). Diversely C8-functionalized adenine nucleosides via their underexplored carboxaldehydes. Chemical Communications. 58(11). 1744–1747. 2 indexed citations
2.
Lakshman, Mahesh K. & Barbara Zajc. (2017). When nucleoside chemistry met hypervalent iodine reagents. ARKIVOC. 2018(2). 252–279. 1 indexed citations
3.
Ayeni, Deborah, Samir Mandal, & Barbara Zajc. (2013). Julia–Kocienski approach to trifluoromethyl-substituted alkenes. Tetrahedron Letters. 54(45). 6008–6011. 17 indexed citations
4.
Mandal, Samir, Arun K. Ghosh, Rakesh Kumar, & Barbara Zajc. (2012). Expedient synthesis of α-substituted fluoroethenes. Organic & Biomolecular Chemistry. 10(16). 3164–3164. 19 indexed citations
5.
Kumar, Rakesh, Padmanava Pradhan, & Barbara Zajc. (2011). Facile synthesis of 4-vinyl- and 4-fluorovinyl-1,2,3-triazoles via bifunctional “click-olefination” reagents. Chemical Communications. 47(13). 3891–3891. 24 indexed citations
6.
Zajc, Barbara & Rakesh Kumar. (2010). Synthesis of Fluoroolefins via Julia-Kocienski Olefination. Synthesis. 2010(11). 1822–1836. 90 indexed citations
7.
Zajc, Barbara. (2009). ChemInform Abstract: Application of Xenon Difluoride in Synthesis. ChemInform. 40(20). 2 indexed citations
8.
Zajc, Barbara, Maggie He, & Arun K. Ghosh. (2008). Julia Olefination as a General Route to Phenyl (α-Fluoro)vinyl Sulfones. Synlett. 2008(7). 999–1004. 13 indexed citations
9.
Kramata, Pavel, et al.. (2003). A Single Site-specific trans-Opened 7,8,9,10-Tetrahydrobenzo[a]pyrene 7,8-Diol 9,10-EpoxideN2-Deoxyguanosine Adduct Induces Mutations at Multiple Sites in DNA. Journal of Biological Chemistry. 278(17). 14940–14948. 13 indexed citations
10.
11.
Simhadri, Srilatha, Pavel Kramata, Barbara Zajc, et al.. (2002). Benzo[a]pyrene diol epoxide–deoxyguanosine adducts are accurately bypassed by yeast DNA polymerase ζ in vitro. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 508(1-2). 137–145. 21 indexed citations
12.
Bastiaans, M.J., et al.. (2001). Time frequency signal representations. TU/e Research Portal (Eindhoven University of Technology). 13–18. 1 indexed citations
13.
Zajc, Barbara, et al.. (1998). Effect of single benzo[a]pyrene diol epoxide-deoxyguanosine adducts on the action of DNA polymerases in vitro.. International Journal of Oncology. 13(2). 269–73. 21 indexed citations
14.
Page, John E., Barbara Zajc, Toshinari Oh-hara, et al.. (1998). Sequence Context Profoundly Influences the Mutagenic Potency of Trans-Opened Benzo[a]pyrene 7,8-Diol 9,10-Epoxide−Purine Nucleoside Adducts in Site-Specific Mutation Studies. Biochemistry. 37(25). 9127–9137. 62 indexed citations
15.
Lakshman, Mahesh K. & Barbara Zajc. (1996). A Rapid, High-Yield Method for 5′-Hydroxyl Protection in Very Reactive and Amino Group Modified Nucleosides Using Dimethoxytrityl Tetrafluoroborate. Nucleosides and Nucleotides. 15(5). 1029–1039. 12 indexed citations
16.
17.
Zajc, Barbara & Mahesh K. Lakshman. (1995). Acyl Migration in Anions Derived from Nonenolizable Esters of Polycyclic Aromatic Hydrocarbons. The Journal of Organic Chemistry. 60(15). 4936–4939. 3 indexed citations
18.
Zajc, Barbara & Marko Zupan. (1989). Bromination of aromatic molecules with polymer supported reagents. Tetrahedron. 45(24). 7869–7878. 21 indexed citations
19.
Zajc, Barbara & Marko Zupan. (1982). Room-temperature Fluorine Addition to Fluoro-substituted Naphthalene Derivative Using Xenon Difluoride. Bulletin of the Chemical Society of Japan. 55(5). 1617–1619. 4 indexed citations
20.
Gregorčič, A., Barbara Zajc, & Marko Zupan. (1979). REACTIONS OF XENON DIFLUORIDE WITH ORGANO-SULPHUR MOLECULES. Phosphorous and Sulfur and the Related Elements. 6(1-2). 107–108. 1 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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