Isidro S. Marcos

810 total citations
56 papers, 631 citations indexed

About

Isidro S. Marcos is a scholar working on Organic Chemistry, Molecular Biology and Cancer Research. According to data from OpenAlex, Isidro S. Marcos has authored 56 papers receiving a total of 631 indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Organic Chemistry, 22 papers in Molecular Biology and 15 papers in Cancer Research. Recurrent topics in Isidro S. Marcos's work include Asymmetric Synthesis and Catalysis (24 papers), Synthetic Organic Chemistry Methods (14 papers) and Sesquiterpenes and Asteraceae Studies (13 papers). Isidro S. Marcos is often cited by papers focused on Asymmetric Synthesis and Catalysis (24 papers), Synthetic Organic Chemistry Methods (14 papers) and Sesquiterpenes and Asteraceae Studies (13 papers). Isidro S. Marcos collaborates with scholars based in Spain, United Kingdom and Portugal. Isidro S. Marcos's co-authors include Julio G. Urones, P. Basabe, Narciso M. Garrido, David Dı́ez, Rosalina F. Moro, Pilar Garcı́a Garcı́a, Anna M. Lithgow, Howard B. Broughton, María José Gil Quílez and Francisca Sanz and has published in prestigious journals such as The Journal of Organic Chemistry, Tetrahedron and Molecules.

In The Last Decade

Isidro S. Marcos

53 papers receiving 611 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Isidro S. Marcos Spain 15 451 219 78 74 67 56 631
Alice Kanazawa France 19 684 1.5× 251 1.1× 62 0.8× 71 1.0× 45 0.7× 37 822
Michiharu Kato Japan 16 608 1.3× 212 1.0× 46 0.6× 59 0.8× 67 1.0× 71 799
Helena M. C. Ferraz Brazil 19 858 1.9× 173 0.8× 64 0.8× 83 1.1× 89 1.3× 72 1.0k
F. Javier Moreno‐Dorado Spain 15 420 0.9× 186 0.8× 84 1.1× 69 0.9× 84 1.3× 36 627
Hassen Amri France 19 895 2.0× 258 1.2× 57 0.7× 84 1.1× 44 0.7× 84 996
P. F. SCHUDA United States 16 641 1.4× 244 1.1× 59 0.8× 56 0.8× 99 1.5× 27 815
Tatsuzo Ukita Japan 15 613 1.4× 281 1.3× 37 0.5× 64 0.9× 30 0.4× 31 787
Yoko Yuasa Japan 14 567 1.3× 198 0.9× 56 0.7× 74 1.0× 27 0.4× 76 661
Paolo Ceccherelli Italy 17 465 1.0× 273 1.2× 61 0.8× 82 1.1× 51 0.8× 71 796
Jean‐Louis Gras France 14 548 1.2× 224 1.0× 32 0.4× 44 0.6× 53 0.8× 40 669

Countries citing papers authored by Isidro S. Marcos

Since Specialization
Citations

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

Fields of papers citing papers by Isidro S. Marcos

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Isidro S. Marcos

This figure shows the co-authorship network connecting the top 25 collaborators of Isidro S. Marcos. A scholar is included among the top collaborators of Isidro S. Marcos 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 Isidro S. Marcos. Isidro S. Marcos 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.
Marcos, Isidro S., et al.. (2016). Crystal structure of (2R*,3aR*)-2-phenylsulfonyl-2,3,3a,4,5,6-hexahydropyrrolo[1,2-b]isoxazole. Acta Crystallographica Section E Crystallographic Communications. 73(1). 85–87.
2.
Garcı́a, Pilar Garcı́a, et al.. (2013). Domino Elimination/Nucleophilic Addition in the Synthesis of Chiral Pyrrolidines. The Journal of Organic Chemistry. 78(14). 7068–7075. 11 indexed citations
3.
Garcı́a, Pilar Garcı́a, et al.. (2012). From isoxazolidines to tetrahydro-1,3-oxazines for the synthesis of chiral pyrrolidines. RSC Advances. 2(29). 11040–11040. 4 indexed citations
4.
Garcı́a, Pilar Garcı́a, Narciso M. Garrido, P. Basabe, et al.. (2012). 1,3-Dipolar cycloaddition of nitrones with phenylvinyl sulfone. An experimental and theoretical study. Tetrahedron Asymmetry. 23(1). 76–85. 10 indexed citations
5.
Moro, Rosalina F., et al.. (2011). Tandem catalysis for the synthesis of 2-alkylidene cyclohexenones. Tetrahedron. 67(43). 8331–8337. 15 indexed citations
6.
Núñez, Marta G., Rosalina F. Moro, Narciso M. Garrido, et al.. (2010). Synthesis of a New Chiral Pyrrolidine. Molecules. 15(3). 1501–1512. 6 indexed citations
7.
Dı́ez, David, Pilar Garcı́a Garcı́a, Rosalina F. Moro, et al.. (2008). Asymmetric Epoxidation of Electron-Deficient Olefins. Current Organic Synthesis. 5(3). 186–216. 82 indexed citations
8.
Garcı́a, Pilar Garcı́a, David Dı́ez, Narciso M. Garrido, et al.. (2007). Stereoselective Synthesis of Cyclopropanols. ChemInform. 38(36).
9.
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
10.
Dı́ez, David, María José Gil Quílez, Rosalina F. Moro, et al.. (2005). Chemistry of sulfones: synthesis of a new chiral nucleophilic catalyst. Tetrahedron Asymmetry. 16(17). 2980–2985. 20 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.
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
13.
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
15.
Dı́ez, David, Pilar Garcı́a Garcı́a, Isidro S. Marcos, et al.. (2002). Diastereoselective Synthesis of Enantiomerically Pure 1,2-Disubstituted Cyclopropanols from Allylic Sulfones. Synlett. 2002(2). 355–357. 5 indexed citations
16.
Dı́ez, David, et al.. (2001). Enantioselective Synthesis of a 2,3,4-Trisubstituted Pyrrolidine from 1-Hydroxymethyl-4-phenylsulfonylbutadiene. Synlett. 2001(5). 655–657. 10 indexed citations
17.
Urones, Julio G., Isidro S. Marcos, P. Basabe, et al.. (1993). Synthesis of Fregenedadiol Dimethyl Ether. Natural product letters. 3(3). 173–176. 5 indexed citations
18.
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
19.
Urones, Julio G., et al.. (1990). Terpenoid compounds from Parentucellia latifolia. Phytochemistry. 29(7). 2223–2228. 10 indexed citations
20.
Urones, Julio G., et al.. (1986). Diterpenoid and other components of Cistus laurifolius. Phytochemistry. 25(5). 1185–1187. 19 indexed citations

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