Lucía S. Andrés

757 total citations
38 papers, 654 citations indexed

About

Lucía S. Andrés is a scholar working on Molecular Biology, Complementary and alternative medicine and Plant Science. According to data from OpenAlex, Lucía S. Andrés has authored 38 papers receiving a total of 654 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 17 papers in Complementary and alternative medicine and 14 papers in Plant Science. Recurrent topics in Lucía S. Andrés's work include Natural product bioactivities and synthesis (18 papers), Traditional Chinese Medicine Analysis (17 papers) and Phytochemistry and Biological Activities (11 papers). Lucía S. Andrés is often cited by papers focused on Natural product bioactivities and synthesis (18 papers), Traditional Chinese Medicine Analysis (17 papers) and Phytochemistry and Biological Activities (11 papers). Lucía S. Andrés collaborates with scholars based in Spain, Mexico and Colombia. Lucía S. Andrés's co-authors include Javier G. Luis, Laila Moujir, Joaquín G. Marrero, A.M. Gutiérrez‐Navarro, Antonio G. González, Ángel G. Ravelo, José M. Padrón, Antonio González, Leticia G. León and Antonio G. González and has published in prestigious journals such as Tetrahedron, Phytochemistry and Tetrahedron Letters.

In The Last Decade

Lucía S. Andrés

36 papers receiving 622 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lucía S. Andrés Spain 17 455 239 190 146 87 38 654
Laxmi N. Misra India 17 291 0.6× 280 1.2× 144 0.8× 197 1.3× 58 0.7× 31 610
Özgen Alankuş‐Çalışkan Türkiye 18 575 1.3× 329 1.4× 245 1.3× 91 0.6× 62 0.7× 49 744
Masayuki YOSHIKAWA Japan 9 319 0.7× 178 0.7× 78 0.4× 105 0.7× 55 0.6× 10 548
Jian-Qiao Gu United States 8 301 0.7× 168 0.7× 96 0.5× 75 0.5× 83 1.0× 8 542
M. Lahloub Egypt 17 504 1.1× 477 2.0× 79 0.4× 139 1.0× 41 0.5× 40 731
Emma Maldonado Mexico 16 453 1.0× 322 1.3× 359 1.9× 181 1.2× 78 0.9× 87 860
Li‐Ming Yang Kuo Taiwan 16 487 1.1× 210 0.9× 157 0.8× 43 0.3× 93 1.1× 23 683
Armin Presser Austria 13 252 0.6× 228 1.0× 52 0.3× 89 0.6× 117 1.3× 38 593
Angela Perrone Italy 20 605 1.3× 333 1.4× 170 0.9× 186 1.3× 67 0.8× 33 923
S. Zschocke Germany 11 228 0.5× 359 1.5× 147 0.8× 128 0.9× 69 0.8× 14 610

Countries citing papers authored by Lucía S. Andrés

Since Specialization
Citations

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

Fields of papers citing papers by Lucía S. Andrés

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lucía S. Andrés. 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 Lucía S. Andrés. The network helps show where Lucía S. Andrés may publish in the future.

Co-authorship network of co-authors of Lucía S. Andrés

This figure shows the co-authorship network connecting the top 25 collaborators of Lucía S. Andrés. A scholar is included among the top collaborators of Lucía S. Andrés 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 Lucía S. Andrés. Lucía S. Andrés 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.
Andrés, Lucía S., et al.. (2013). Rosmanol controls explants browing of Hypericum canariensis L. during the in vitro estabilishment of shoots. Acta Societatis Botanicorum Poloniae. 66(3-4). 347–349.
2.
Marrero, Joaquín G., Lucía S. Andrés, & Javier G. Luis. (2013). Synthesis of Diterpenoid Rosmic Acid Derivatives. Journal of Chemical Research. 37(4). 193–196. 2 indexed citations
3.
Marrero, Joaquín G., et al.. (2009). Semisynthesis and Biological Evaluation of Abietane-Type Diterpenes. Revision of the Structure of Rosmaquinone. Journal of Natural Products. 72(8). 1385–1389. 21 indexed citations
4.
Córdova, I., et al.. (2007). Synthesis and Antiproliferative Activity of Novel Sugiol β‐Amino Alcohol Analogues.. ChemInform. 38(12). 1 indexed citations
5.
Córdova, I., et al.. (2006). Synthesis and antiproliferative activity of novel sugiol β-amino alcohol analogs. European Journal of Medicinal Chemistry. 41(11). 1327–1332. 25 indexed citations
6.
Andrés, Lucía S., Leticia G. León, Rubén P. Machín, et al.. (2006). Abietane Diterpenoids from Salvia pachyphylla and S. clevelandii with Cytotoxic Activity against Human Cancer Cell Lines. Journal of Natural Products. 69(12). 1803–1805. 55 indexed citations
7.
Moujir, Laila, Jesús Burillo, Mónica González, et al.. (2005). Chemical composition and biological activities of the essential oils ofSalvia canariensis. Flavour and Fragrance Journal. 21(1). 72–76. 19 indexed citations
8.
Marrero, Joaquín G., Lucía S. Andrés, & Javier G. Luis. (2005). Quinone Derivatives by Chemical Transformations of 16-Hydroxycarnosol from Salvia Species. Chemical and Pharmaceutical Bulletin. 53(12). 1524–1529. 15 indexed citations
9.
Moujir, Laila, Jesús Burillo, Mónica González, et al.. (2005). Chemical composition and biological activities of the essential oils ofSalvia canariensis. Flavour and Fragrance Journal. 21(2). 277–281. 11 indexed citations
10.
Luis, Javier G., et al.. (1999). 4′-Dehydroxy-Irenolone. A New Phytoanticipin from the Resistant Musa Selected Hybrid SH-3481. Natural product letters. 14(2). 147–152. 4 indexed citations
11.
Luis, Javier G., et al.. (1997). Phenylphenalenonic phytoanticipins. New acenaphtylene and dimeric phenylphenalenones from the resistant Musa selected hybrid SH-3481. Tetrahedron. 53(24). 8249–8256. 20 indexed citations
12.
Moujir, Laila, et al.. (1996). Bioactive Diterpenoids Isolated from Salvia mellifera. Phytotherapy Research. 10(2). 172–174. 4 indexed citations
13.
Moujir, Laila, A.M. Gutiérrez‐Navarro, Lucía S. Andrés, & Javier G. Luis. (1993). Structure—antimicrobial activity relationships of abietane diterpenes from Salvia species. Phytochemistry. 34(6). 1493–1495. 49 indexed citations
14.
Luis, Javier G., Lucía S. Andrés, & Áurea Perales. (1993). C-16 hydroxylated abietane diterpenes from salvia mellifera. Absolute configuration and biogenetic implications.. Tetrahedron. 49(22). 4993–5000. 14 indexed citations
15.
Luis, Javier G., et al.. (1992). Diterpenes from in vitro-grown Salvia canariensis. Phytochemistry. 31(9). 3272–3273. 15 indexed citations
16.
González, Antonio, et al.. (1991). A New Friedooleane Triterpenic Acid from Schaefferia cuneifolia. Journal of Natural Products. 54(2). 585–587. 2 indexed citations
17.
González, Antonio, Lucía S. Andrés, Ángel G. Ravelo, et al.. (1990). Terpenoids from Salvia mellifera. Phytochemistry. 29(5). 1691–1693. 19 indexed citations
18.
González, Antonio G., et al.. (1989). Abietane diterpenes with antibiotic activity from the flowers of Salviacanariensis. Reaction of galdosol with diazomethane. Canadian Journal of Chemistry. 67(2). 208–212. 32 indexed citations
19.
20.
González, Antonio, et al.. (1989). Minor Constituents from Orthosphenia mexicana. Journal of Natural Products. 52(6). 1338–1341. 14 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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