J.L. Kraus

628 total citations
33 papers, 459 citations indexed

About

J.L. Kraus is a scholar working on Organic Chemistry, Infectious Diseases and Virology. According to data from OpenAlex, J.L. Kraus has authored 33 papers receiving a total of 459 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Organic Chemistry, 12 papers in Infectious Diseases and 9 papers in Virology. Recurrent topics in J.L. Kraus's work include HIV/AIDS drug development and treatment (12 papers), HIV Research and Treatment (9 papers) and Click Chemistry and Applications (6 papers). J.L. Kraus is often cited by papers focused on HIV/AIDS drug development and treatment (12 papers), HIV Research and Treatment (9 papers) and Click Chemistry and Applications (6 papers). J.L. Kraus collaborates with scholars based in France, Canada and Germany. J.L. Kraus's co-authors include B. Belleau, Xiaojian Yao, Qing Gao, Nghe Nguyen‐Ba, Bonnie Spira, Mark A. Wainberg, Hugo Soudeyns, Michel Camplo, J. Linek and Gerhard Franz and has published in prestigious journals such as Antimicrobial Agents and Chemotherapy, Molecular Pharmacology and European Journal of Cancer.

In The Last Decade

J.L. Kraus

32 papers receiving 437 citations

Peers

Countries citing papers authored by J.L. Kraus

Since Specialization

Citations

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

Fields of papers citing papers by J.L. Kraus

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J.L. Kraus. 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 J.L. Kraus. The network helps show where J.L. Kraus may publish in the future.

Co-authorship network of co-authors of J.L. Kraus

This figure shows the co-authorship network connecting the top 25 collaborators of J.L. Kraus. A scholar is included among the top collaborators of J.L. Kraus 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 J.L. Kraus. J.L. Kraus 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

#	Work	Indexed citations
1	Synthesis and biological activity of phosphonate analogues and geometric isomers of the highly potent phosphoantigen (E)-1-hydroxy-2-methylbut-2-enyl 4-diphosphate 2008 ·HAL (Le Centre pour la Communication Scientifique Directe) ·(unknown), Hélène Sicard, (unknown), (unknown), Sophie Ingoure, (unknown), Christian Belmant, J.L. Kraus	2
2	New anti-HIV derivatives: synthesis and antiviral evaluation 2000 ·Bioorganic & Medicinal Chemistry ·(unknown), (unknown), (unknown), Jean‐Claude Chermann, J.L. Kraus	5
3	Synthesis and chemical reactivity of thiophenoxyphenylalanine bioisosteres, suitable synthons for the design of HIV protease inhibitors 2000 ·Journal of the Chemical Society Perkin Transactions 1 ·(unknown), (unknown), (unknown), Jérôme Courcambeck, J.L. Kraus	5
4	Synthesis and Biological Evaluation of Polyaminated 2′,3′-Dideoxy-3′-thiacytidine Prodrugs 1999 ·Nucleosides and Nucleotides ·Michel Camplo, (unknown), Chermann Jc, J.L. Kraus	2
5	Syntheses of new modified Phe-Pro peptides. Use of proline replacements in potential HIV inhibitors 1998 ·Bioorganic & Medicinal Chemistry Letters ·(unknown), (unknown), (unknown), Jean‐Claude Chermann, Michel Camplo, J.L. Kraus	5
6	Tri-N-Boc-Tetraazamacrocycle-Nucleoside Conjugates: Synthesis and anti-HIV activities 1998 ·Nucleosides and Nucleotides ·Jean Dessolin, Patrick Vlieghe, (unknown), (unknown), (unknown), Michel Camplo, Chermann Jc, J.L. Kraus	6
7	Syntheses of new unsymmetrical bispolyazamacrocycles 1998 ·Tetrahedron Letters ·Jean Dessolin, (unknown), Michel Camplo, J.L. Kraus	4
8	A model allowing the design of modified nucleosides as HIV-RT inhibitors 1996 ·European Journal of Medicinal Chemistry ·(unknown), (unknown), (unknown), (unknown), Chermann Jc, J.L. Kraus	5
9	Modelisation, synthesis and antiviral evaluation of new 2,3-disubstituted thiazolidinone nucleoside analogues 1996 ·Bioorganic & Medicinal Chemistry Letters ·(unknown), (unknown), (unknown), (unknown), Jean Dessolin, (unknown), (unknown), Fabien Zoulim, Christelle Borel, O. Hantz, Michel Camplo, Chermann Jc, J.L. Kraus	6
10	Synthesis and antiviral activity of N-4′-dihydropyridinyl and dihydroquinolinylcarbonyl-2-hydroxymethyl-5-[cytosin-1′-yl]-1,3-oxathiolane derivatives against human immunodeficiency virus and duck hepatitis B virus 1996 ·European Journal of Medicinal Chemistry ·Michel Camplo, (unknown), Christelle Borel, (unknown), O. Hantz, (unknown), (unknown), (unknown), (unknown), Chermann Jc, J.L. Kraus	7
11	Synthesis and comparative anti-HIV activities of new acetylated 2′,3′-dideoxy-3′-thiacytidine analogues 1994 ·European Journal of Medicinal Chemistry ·Michel Camplo, (unknown), (unknown), (unknown), Chermann Jc, J.L. Kraus	9
12	Synthesis of laminarin sulfates with anticoagulant activity. 1992 ·PubMed ·Susanne Alban, J.L. Kraus, Gerhard Franz	24
13	Design and activity of a novel class of nucleoside analogs effective against hiv 1 1989 ·B. Belleau, (unknown), (unknown), J.L. Kraus	9
14	Isosterism and molecular modification in drug design : Tetrazole analogue of GABA : Effects on enzymes of the γ-aminobutyrate system 1983 ·Pharmacological Research Communications ·J.L. Kraus	20
15	Isoterism and molecular modification in drug design: New n-dipropylacetate analogs as inhibitors of succinic semi aldehyde dehydrogenase 1983 ·Pharmacological Research Communications ·J.L. Kraus	3
16	Synthese d'analogues tetrazoles de l'acide phosphonoacetique 1980 ·Tetrahedron Letters ·Jean‐Jacques Yaouanc, G. STURTZ, J.L. Kraus, (unknown), (unknown)	12
17	Inhibition of the cytochrome P-450 multifunctional oxidase by N-propargyl analogs of SKF-525A and acetylmethadol 1979 ·European Journal of Drug Metabolism and Pharmacokinetics ·J.L. Kraus, Jean‐Jacques Yaouanc	1
18	Inactivation of a Flavin-Linked Oxidase, N,N-Dimethylglycine Oxidase, in Vivo and in Vitro 1977 ·Molecular Pharmacology ·J.L. Kraus, Jean‐Jacques Yaouanc	5
19	Liquid-vapour equilibrium. XLVIII. The systems acetone-benzene, acetone-toluene, benzene-methyl ethyl ketone, methyl ethyl ketone-toluene and methyl ethyl ketone-ethylbenzene 1971 ·Collection of Czechoslovak Chemical Communications ·J.L. Kraus, J. Linek	21
20	Die energiereichen Phosphate in der M�useniere unter Einwirkung von Inulin und Harnstoff 1960 ·Pflügers Archiv - European Journal of Physiology ·(unknown), G. Hierholzer, J.L. Kraus, Joachim Frey	1

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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