P. Basabe

2.4k total citations
134 papers, 2.0k citations indexed

About

P. Basabe is a scholar working on Organic Chemistry, Molecular Biology and Cancer Research. According to data from OpenAlex, P. Basabe has authored 134 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 80 papers in Organic Chemistry, 62 papers in Molecular Biology and 35 papers in Cancer Research. Recurrent topics in P. Basabe's work include Synthetic Organic Chemistry Methods (41 papers), Sesquiterpenes and Asteraceae Studies (33 papers) and Marine Sponges and Natural Products (32 papers). P. Basabe is often cited by papers focused on Synthetic Organic Chemistry Methods (41 papers), Sesquiterpenes and Asteraceae Studies (33 papers) and Marine Sponges and Natural Products (32 papers). P. Basabe collaborates with scholars based in Spain, United Kingdom and Portugal. P. Basabe's co-authors include Julio G. Urones, David Dı́ez, Isidro S. Marcos, Rosalina F. Moro, Isidro S. Marcos, Narciso M. Garrido, Anna M. Lithgow, Howard B. Broughton, Pilar Garcı́a Garcı́a and Faustino Mollinedo and has published in prestigious journals such as The Journal of Organic Chemistry, Tetrahedron and Molecules.

In The Last Decade

P. Basabe

132 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
P. Basabe Spain 23 1.1k 831 544 268 253 134 2.0k
Julio G. Urones Spain 25 1.3k 1.2× 1.2k 1.4× 560 1.0× 400 1.5× 261 1.0× 176 2.5k
David Dı́ez Spain 26 1.8k 1.6× 1.0k 1.3× 596 1.1× 221 0.8× 329 1.3× 206 2.8k
Masayoshi Ando Japan 25 1.0k 0.9× 771 0.9× 168 0.3× 252 0.9× 231 0.9× 93 2.0k
Isidro S. Marcos Spain 23 771 0.7× 854 1.0× 526 1.0× 280 1.0× 262 1.0× 112 1.8k
Haruaki Ishiyama Japan 26 1.1k 1.0× 406 0.5× 398 0.7× 120 0.4× 382 1.5× 57 1.6k
Shigefumi Kuwahara Japan 25 1.4k 1.2× 724 0.9× 286 0.5× 118 0.4× 561 2.2× 211 2.5k
Mark A. Rizzacasa Australia 24 1.3k 1.2× 805 1.0× 288 0.5× 97 0.4× 317 1.3× 105 2.1k
Enrique Álvarez‐Manzaneda Spain 24 827 0.7× 732 0.9× 399 0.7× 119 0.4× 282 1.1× 86 1.6k
Rosalina F. Moro Spain 20 711 0.6× 530 0.6× 260 0.5× 118 0.4× 157 0.6× 71 1.3k
Juan F. Sanz‐Cervera Spain 33 1.8k 1.6× 1.2k 1.5× 187 0.3× 278 1.0× 511 2.0× 90 2.8k

Countries citing papers authored by P. Basabe

Since Specialization
Citations

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

Fields of papers citing papers by P. Basabe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of P. Basabe

This figure shows the co-authorship network connecting the top 25 collaborators of P. Basabe. A scholar is included among the top collaborators of P. Basabe 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 P. Basabe. P. Basabe 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.
Martín, María Luisa, et al.. (2015). Biomimetic Synthesis of Two Salmahyrtisanes: Salmahyrtisol A and Hippospongide A. The Journal of Organic Chemistry. 80(9). 4566–4572. 10 indexed citations
2.
Marcos, Isidro S., Rosalina F. Moro, P. Basabe, et al.. (2014). Synthesis and biological activity of polyalthenol and pentacyclindole analogues. European Journal of Medicinal Chemistry. 73. 265–279. 11 indexed citations
3.
Marcos, Isidro S., et al.. (2013). Sesquiterpenyl indoles. Natural Product Reports. 30(12). 1509–1509. 90 indexed citations
4.
Moro, Rosalina F., et al.. (2012). Solvent free l-proline-catalysed domino Knoevenagel/6π-electrocyclization for the synthesis of highly functionalised 2H-pyrans. RSC Advances. 2(21). 8041–8041. 10 indexed citations
5.
Basabe, P., et al.. (2010). Prenylflavonoids and prenyl/alkyl-phloroacetophenones: Synthesis and antitumour biological evaluation☆. European Journal of Medicinal Chemistry. 45(9). 4258–4269. 36 indexed citations
6.
Marcos, Isidro S., et al.. (2008). Synthetic studies to highly functionalised B ring labdanes. Tetrahedron. 64(37). 8815–8829. 11 indexed citations
7.
Marcos, Isidro S., Rosalina F. Moro, P. Basabe, et al.. (2007). Synthesis of novel antitumoural analogues of dysidiolide from ent-halimic acid. Bioorganic & Medicinal Chemistry. 15(17). 5719–5737. 32 indexed citations
8.
Garcı́a, Pilar Garcı́a, David Dı́ez, Narciso M. Garrido, et al.. (2007). Stereoselective Synthesis of Cyclopropanols. ChemInform. 38(36).
9.
Basabe, P., et al.. (2007). Synthesis of (+)-lagerstronolide from (+)-sclareol. Tetrahedron. 63(48). 11838–11843. 21 indexed citations
10.
Dı́ez, David, María José Gil Quílez, Rosalina F. Moro, et al.. (2006). A new class of chiral pyrrolidine for asymmetric Michael addition reactions. New mechanism via simple 4+2 type attack of the enamine on the trans-nitrostyrene. Tetrahedron. 63(3). 740–747. 32 indexed citations
11.
Dı́ez, David, Pilar Garcı́a Garcı́a, Isidro S. Marcos, et al.. (2005). Vinylsulfones versus alkylsulfones in the addition to chiral imines. Synthesis of N-(tert-butoxycarbonyl)-l-homophenylalanine. Tetrahedron. 61(49). 11641–11648. 4 indexed citations
12.
Dı́ez, David, Pilar Garcı́a Garcı́a, Isidro S. Marcos, et al.. (2003). Stereocontrolled Synthesis of Cyclopropanol Amino Acids from Allylic Sulfones:  Conformationally Restricted Building Blocks. Organic Letters. 5(20). 3687–3690. 20 indexed citations
13.
Marcos, Isidro S., Rosalina F. Moro, David Dı́ez, et al.. (2003). Synthesis of (+)-totarol. Tetrahedron Letters. 44(49). 8831–8835. 11 indexed citations
14.
Basabe, P., et al.. (2003). Short and efficient synthesis of (+)-subersic acids. Tetrahedron. 59(46). 9173–9177. 23 indexed citations
15.
Marcos, Isidro S., David Dı́ez, P. Basabe, et al.. (2003). Synthesis and absolute configuration of (−)-chrysolic acid and (+)-isofregenedol. Tetrahedron Letters. 44(29). 5419–5422. 16 indexed citations
16.
Marcos, Isidro S., J. L. González, David Dı́ez, et al.. (2000). Diterpenic α- and β-hydroxybutanolides with antifeedant activity: semisynthesis and absolute configuration. Tetrahedron Letters. 41(15). 2553–2557. 17 indexed citations
17.
Basabe, P., Antonio Bermejo Gómez, Isidro S. Marcos, et al.. (1999). Towards the synthesis of 9,11-secospongianes. Tetrahedron Letters. 40(37). 6857–6860. 4 indexed citations
18.
Urones, Julio G., et al.. (1995). 2α,3β-dihydroxy-4(18)-neo-cleroden-15-oic acid from cistus populifolius. Phytochemistry. 38(2). 443–445. 4 indexed citations
19.
Urones, Julio G., et al.. (1992). Chemistry of labdanediol from Cistus ladaniferus, L. synthesis of 12-Nor-ambreinolide and α and β-levantenolides. Tetrahedron. 48(47). 10389–10398. 22 indexed citations
20.
Urones, Julio G., et al.. (1990). ent-Halimane diterpenes from Halimium viscosum. Phytochemistry. 29(4). 1247–1251. 17 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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