Dimiter D. Petkov

652 total citations
49 papers, 543 citations indexed

About

Dimiter D. Petkov is a scholar working on Molecular Biology, Organic Chemistry and Oncology. According to data from OpenAlex, Dimiter D. Petkov has authored 49 papers receiving a total of 543 indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Molecular Biology, 16 papers in Organic Chemistry and 6 papers in Oncology. Recurrent topics in Dimiter D. Petkov's work include DNA and Nucleic Acid Chemistry (17 papers), Chemical Synthesis and Analysis (16 papers) and RNA and protein synthesis mechanisms (14 papers). Dimiter D. Petkov is often cited by papers focused on DNA and Nucleic Acid Chemistry (17 papers), Chemical Synthesis and Analysis (16 papers) and RNA and protein synthesis mechanisms (14 papers). Dimiter D. Petkov collaborates with scholars based in Bulgaria, Germany and Finland. Dimiter D. Petkov's co-authors include Ivanka Stoineva, Miroslav Rangelov, Georgi N. Vayssilov, Ilkka Mononen, Svetomir B. Tzokov, Magda Anastassova Dineva, Boris Galunsky, Volker Kasche, Nikolay Vassilev and Gabriela D. Ivanova and has published in prestigious journals such as Journal of the American Chemical Society, Journal of Biological Chemistry and Angewandte Chemie International Edition.

In The Last Decade

Dimiter D. Petkov

49 papers receiving 520 citations

Peers

Dimiter D. Petkov

ONCOL

SPECT

BIOTE

K. K. Bhandary United States

Kurt W. Saionz United States

James Aikins United States

J. Bergmann Germany

Christelle Tardy France

Nichola L. Davies United Kingdom

Kang Man Lee South Korea

Branimir Bertoša Croatia

L. Kittler Austria

Gottfried K. Schroeder United States

K. K. Bhandary United States

Dimiter D. Petkov

387 ×0.9

204 ×1.2

72 ×0.8

ONCOL

44 ×0.9

SPECT

27 ×0.6

BIOTE

Citations per year, relative to Dimiter D. Petkov Dimiter D. Petkov (= 1×) peers K. K. Bhandary

Countries citing papers authored by Dimiter D. Petkov

Since Specialization

Citations

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

Fields of papers citing papers by Dimiter D. Petkov

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dimiter D. Petkov. 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 Dimiter D. Petkov. The network helps show where Dimiter D. Petkov may publish in the future.

Co-authorship network of co-authors of Dimiter D. Petkov

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

All Works

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20 of 20 papers shown

Vassilev, Nikolay, et al.. (2010). The Two Pathways for Effective Orthogonal Protection of L-Ornithine, for Amino Acylation of 5-O-Pivaloyl Nucleosides, Describe the General and Important Role for the Successful Imitation, During the Synthesis of the Model Substrates for the Ribosomal Mimic Reaction. Protein and Peptide Letters. 17(7). 889–898. 2 indexed citations

Vassilev, Nikolay, et al.. (2009). Design and Synthesis of Substrates for Model Ribosomal Reactions. Protein and Peptide Letters. 16(4). 392–401. 2 indexed citations

Ivanova, Gabriela D., Miroslav Rangelov, Parag Acharya, et al.. (2005). 2′/3′‐O‐peptidyl Adenosine as a General Base Catalyst of its Own External Peptidyl Transfer: Implications for the Ribosome Catalytic Mechanism. ChemBioChem. 6(6). 992–996. 26 indexed citations

Rangelov, Miroslav, et al.. (2005). Theoretical study of the o-OH participation in catechol ester ammonolysis. Organic & Biomolecular Chemistry. 3(5). 737–737. 13 indexed citations

Stoineva, Ivanka, et al.. (2002). β‐Aspartylpeptides as substrates of L‐asparaginases from Escherichia coli and Erwinia chrysanthemi. FEBS Letters. 528(1-3). 130–132. 29 indexed citations

Petkov, Dimiter D., et al.. (2001). Catechol as a nucleophilic catalyst of peptide bond formation. Journal of Peptide Science. 8(1). 8–12. 15 indexed citations

Ivanova, Gabriela D., et al.. (1999). External Transesterification of Ribonucleotide Esters Naturally Catalyzed by Large Ribozymes. Journal of the American Chemical Society. 121(49). 11267–11272. 12 indexed citations

Stoineva, Ivanka, et al.. (1998). Glycosylasparaginase-catalyzed Synthesis and Hydrolysis of β-Aspartyl Peptides. Journal of Biological Chemistry. 273(41). 26295–26297. 19 indexed citations

Stoineva, Ivanka, et al.. (1997). Recombinant human glycosylasparaginase catalyzes hydrolysis of l‐asparagine. FEBS Letters. 412(1). 149–152. 17 indexed citations

10.

Ivanov, Ivaylo P., et al.. (1996). Semispecific Ester Substrates of Trypsin as Acyl Donors in Kinetically Controlled Peptide Synthesis. Biocatalysis and Biotransformation. 14(3). 195–204. 2 indexed citations

11.

Mononen, Ilkka, et al.. (1996). Enzymatic Synthesis of the N-Glycosidic Bond by β-Aspartylation of Glycosylamines. Biochemical and Biophysical Research Communications. 218(2). 510–513. 4 indexed citations

12.

Dineva, Magda Anastassova, et al.. (1993). Complete template-directed enzymatic synthesis of a potential antisense DNA containing 42 methylphosphonodiester bonds. Bioorganic & Medicinal Chemistry. 1(6). 411–414. 16 indexed citations

13.

Todorov, Nikolay P., et al.. (1993). Thermodynamics of enzymic synthesis of solid-phase peptides. Tetrahedron. 49(11). 2307–2316. 2 indexed citations

14.

Stoineva, Ivanka, et al.. (1992). Enzymic synthesis design and enzymic synthesis of aspartame. Tetrahedron. 48(6). 1115–1122. 21 indexed citations

15.

Petkov, Dimiter D., et al.. (1987). Glycine flanked by hydrophobic bulky amino acid residues as minimal sequence for effective subtilisin catalysis. Biochemical Journal. 248(3). 957–960. 19 indexed citations

16.

Petkov, Dimiter D. & Ivanka Stoineva. (1984). Enzyme peptide synthesis by an iterative procedure in a nucleophile pool. Tetrahedron Letters. 25(34). 3751–3754. 20 indexed citations

17.

Petkov, Dimiter D., et al.. (1984). Nucleophile specificity in chymotrypsin peptide synthesis. Biochemical and Biophysical Research Communications. 118(1). 317–323. 41 indexed citations

18.

Petkov, Dimiter D. & Ivanka Stoineva. (1980). The steric effect of the leaving group in the α-chymotrypsin-catalyzed hydrolysis of acetyl-l-phenylalanine p-alkoxycarbonyl anilides. Bioorganic Chemistry. 9(3). 318–324. 6 indexed citations

19.

Petkov, Dimiter D.. (1978). Detection of a tetrahedral intermediate in the trypsin-catalysed hydrolysis of specific ring-activated anilides. Biochimica et Biophysica Acta (BBA) - Enzymology. 523(2). 538–541. 11 indexed citations

20.

Petkov, Dimiter D., et al.. (1973). Amidase activity of urokinase. I. Hydrolysis of alpha-N-acetyl-L-lysine p-nitroanilide.. PubMed. 29(2). 276–85. 4 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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