Françoise Khuong‐Huu

978 total citations
57 papers, 740 citations indexed

About

Françoise Khuong‐Huu is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, Françoise Khuong‐Huu has authored 57 papers receiving a total of 740 indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Organic Chemistry, 26 papers in Molecular Biology and 8 papers in Pharmacology. Recurrent topics in Françoise Khuong‐Huu's work include Synthetic Organic Chemistry Methods (12 papers), Oxidative Organic Chemistry Reactions (10 papers) and Natural product bioactivities and synthesis (8 papers). Françoise Khuong‐Huu is often cited by papers focused on Synthetic Organic Chemistry Methods (12 papers), Oxidative Organic Chemistry Reactions (10 papers) and Natural product bioactivities and synthesis (8 papers). Françoise Khuong‐Huu collaborates with scholars based in France, United States and Republic of the Congo. Françoise Khuong‐Huu's co-authors include Denyse Herlem, R Goutarel, C. Riche, A. Chiaroni, G. LUKACS, Troels Skrydstrup, Angelina Flores‐Parra, Qui Khuong‐Huu, Jean Guilhem and Andrew S. Kende and has published in prestigious journals such as The Journal of Organic Chemistry, Tetrahedron and Phytochemistry.

In The Last Decade

Françoise Khuong‐Huu

54 papers receiving 696 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Françoise Khuong‐Huu France 18 407 267 115 111 82 57 740
Ferdinand Näf Switzerland 17 489 1.2× 282 1.1× 85 0.7× 50 0.5× 60 0.7× 28 812
Yukimasa Terada Japan 18 318 0.8× 381 1.4× 135 1.2× 83 0.7× 169 2.1× 69 845
RC Cambie New Zealand 16 469 1.2× 404 1.5× 170 1.5× 51 0.5× 107 1.3× 130 950
Mabry Benson United States 16 230 0.6× 537 2.0× 202 1.8× 78 0.7× 84 1.0× 44 890
Isao Horibe Japan 16 258 0.6× 382 1.4× 185 1.6× 62 0.6× 141 1.7× 57 806
Hirosuke Yoshioka Japan 19 610 1.5× 324 1.2× 274 2.4× 101 0.9× 54 0.7× 93 1.2k
Koppaka V. Rao United States 16 264 0.6× 424 1.6× 174 1.5× 62 0.6× 189 2.3× 50 880
Lydia Rodríguez‐Hahn Mexico 19 334 0.8× 612 2.3× 310 2.7× 74 0.7× 91 1.1× 68 1.0k
K. H. Overton United Kingdom 17 346 0.9× 619 2.3× 218 1.9× 85 0.8× 100 1.2× 98 1.1k
N. S. Narasimhan India 20 678 1.7× 269 1.0× 165 1.4× 48 0.4× 149 1.8× 60 1.0k

Countries citing papers authored by Françoise Khuong‐Huu

Since Specialization
Citations

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

Fields of papers citing papers by Françoise Khuong‐Huu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Françoise Khuong‐Huu. 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 Françoise Khuong‐Huu. The network helps show where Françoise Khuong‐Huu may publish in the future.

Co-authorship network of co-authors of Françoise Khuong‐Huu

This figure shows the co-authorship network connecting the top 25 collaborators of Françoise Khuong‐Huu. A scholar is included among the top collaborators of Françoise Khuong‐Huu 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 Françoise Khuong‐Huu. Françoise Khuong‐Huu 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.
Bignon, Jérôme, et al.. (2009). A novel iodomethylene-dimethyl-dihydropyranone induces G2/M arrest and apoptosis in human cancer cells.. PubMed. 29(6). 1963–9. 3 indexed citations
2.
Prangé, T., et al.. (2001). Stereoselective allylic transposition by means of allylic n-pentenyl ethers. Part 2: Synthesis of nitrogen heterocycles. Tetrahedron. 57(29). 6229–6238. 2 indexed citations
3.
Chiaroni, A., et al.. (2000). New limonoids fromHarrisonia perforata(Blanco) Merr.. Acta Crystallographica Section C Crystal Structure Communications. 56(6). 711–713. 7 indexed citations
4.
Chiaroni, A., Daniel Guénard, Françoise Guéritte-Voegelein, et al.. (1995). A Baccatin III Derivative. Acta Crystallographica Section C Crystal Structure Communications. 51(3). 465–468. 1 indexed citations
5.
Calatayud, Paul‐André, Yvan Rahbé, B. Delobel, et al.. (1994). Influence of secondary compounds in the phloem sap of cassava on expression of antibiosis towards the mealybug Phenacoccus manihoti. Entomologia Experimentalis et Applicata. 72(1). 47–57. 38 indexed citations
6.
Herlem, Denyse, J. Kervagoret, Dahai Yu, Françoise Khuong‐Huu, & Andrew S. Kende. (1993). Studies toward the total synthesis of polyoxygenated labdanes: preliminary approaches. Tetrahedron. 49(3). 607–618. 17 indexed citations
7.
Skrydstrup, Troels, et al.. (1993). Stereoselective allylic transposition by means of allylic n-pentenyl ethers. Tetrahedron Letters. 34(40). 6407–6410. 8 indexed citations
8.
Nguyen-Ngoc, Hieu, et al.. (1993). Study of cerleaside A, a glycoside from Cerbera odollam. Acta Crystallographica Section C Crystal Structure Communications. 49(11). 2020–2022.
9.
Herlem, Denyse, Françoise Khuong‐Huu, & Andrew S. Kende. (1993). Total synthesis of crotomachlin. Tetrahedron Letters. 34(35). 5587–5590. 5 indexed citations
10.
Delpech, Bernard, et al.. (1992). Total synthesis of maytansinoids. Approach to 4,6-bisdemethylmaytansine and 4-demethylmaytansine. Tetrahedron. 48(10). 1895–1910. 5 indexed citations
11.
Chiaroni, A., et al.. (1990). Crotocorylifuran and crotohaumanoxide, new diterpenes from Croton Haumanianus J. Leonard. Tetrahedron. 46(15). 5199–5202. 18 indexed citations
12.
Flores‐Parra, Angelina & Françoise Khuong‐Huu. (1986). Une approche de synthese de l'enterocine addition de carbanions α-soufres sur le quinide.. Tetrahedron. 42(21). 5925–5930. 15 indexed citations
13.
Khuong‐Huu, Françoise, et al.. (1982). Alcaloides imidazoliques—VI. Tetrahedron. 38(17). 2687–2695. 22 indexed citations
14.
Khuong‐Huu, Françoise, A. Chiaroni, & C. Riche. (1981). Structure of koumine, an alkaloid from benth. Tetrahedron Letters. 22(8). 733–734. 19 indexed citations
15.
Herlem, Denyse, et al.. (1977). Oxydation photochimique D'amines tertiaires et D'alcaloïdes—VIII. Tetrahedron. 33(18). 2389–2392. 29 indexed citations
17.
Khuong‐Huu, Françoise, et al.. (1973). Alcaloïdes steroidiques du Malouetia Brachyloba et du M. Heudelotii. Phytochemistry. 12(7). 1813–1816. 6 indexed citations
19.
Khuong‐Huu, Françoise, et al.. (1970). [Steroidal alkaloids XCVI. Buxaceae family (13th communication). Alkaloids of Buxus malayana Ridl.: cycloprotobuxine C, cyclovirobuxine C, N-formyl cyclovirobuxine B, O-vanillyl cyclovirobuxine B, cyclobuxophylline M].. PubMed. 28(3). 211–22. 4 indexed citations
20.
Khuong‐Huu, Françoise, et al.. (1969). [Steroid alkaloids. LXXXI. The Buxacae family (12th communication). Study of the Wolff-Kishner reduction of the 9 beta, 19 cyclo 11-keto system, and of N-3-isobutyryl cycloxobuxine-F, and of N-3-isobutyryl cycloxobuxidine-F].. PubMed. 1. 258–62. 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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