Alfonso Pérez‐Encabo

677 total citations
35 papers, 540 citations indexed

About

Alfonso Pérez‐Encabo is a scholar working on Organic Chemistry, Molecular Biology and Spectroscopy. According to data from OpenAlex, Alfonso Pérez‐Encabo has authored 35 papers receiving a total of 540 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Organic Chemistry, 12 papers in Molecular Biology and 6 papers in Spectroscopy. Recurrent topics in Alfonso Pérez‐Encabo's work include Asymmetric Synthesis and Catalysis (17 papers), Synthetic Organic Chemistry Methods (11 papers) and Chemical Synthesis and Analysis (10 papers). Alfonso Pérez‐Encabo is often cited by papers focused on Asymmetric Synthesis and Catalysis (17 papers), Synthetic Organic Chemistry Methods (11 papers) and Chemical Synthesis and Analysis (10 papers). Alfonso Pérez‐Encabo collaborates with scholars based in Spain and Vietnam. Alfonso Pérez‐Encabo's co-authors include Rafaël Pedrosa, José M. Andrés, M. Alejandra Martínez, Celia Andrés, Yolanda Castro, Alma M. Astudillo, Jesús Balsinde, Marı́a A. Balboa, Clara Meana and Alicia Maestro and has published in prestigious journals such as Journal of the American Chemical Society, Inorganic Chemistry and The Journal of Organic Chemistry.

In The Last Decade

Alfonso Pérez‐Encabo

34 papers receiving 526 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alfonso Pérez‐Encabo Spain 15 468 167 83 49 42 35 540
M. Serajul Haque United States 12 479 1.0× 175 1.0× 75 0.9× 32 0.7× 35 0.8× 17 575
Yoshitsugu Arai Japan 15 597 1.3× 130 0.8× 67 0.8× 54 1.1× 26 0.6× 43 651
Jacqueline H. Smitrovich United States 16 760 1.6× 132 0.8× 148 1.8× 46 0.9× 24 0.6× 23 829
Yoshitaka Araki Japan 14 432 0.9× 127 0.8× 125 1.5× 41 0.8× 26 0.6× 28 559
Timothy T. Curran United States 16 617 1.3× 225 1.3× 90 1.1× 52 1.1× 57 1.4× 40 772
Fausta Ulgheri Italy 11 358 0.8× 128 0.8× 60 0.7× 29 0.6× 23 0.5× 24 408
Ulrich Zutter Switzerland 9 472 1.0× 238 1.4× 211 2.5× 44 0.9× 25 0.6× 10 599
Genji Iwasaki Japan 14 279 0.6× 210 1.3× 44 0.5× 32 0.7× 23 0.5× 36 481
Wolfgang Bettray Germany 12 584 1.2× 207 1.2× 138 1.7× 47 1.0× 50 1.2× 15 655
Pietro Spanu Italy 13 392 0.8× 205 1.2× 26 0.3× 34 0.7× 28 0.7× 26 443

Countries citing papers authored by Alfonso Pérez‐Encabo

Since Specialization
Citations

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

Fields of papers citing papers by Alfonso Pérez‐Encabo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alfonso Pérez‐Encabo. 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 Alfonso Pérez‐Encabo. The network helps show where Alfonso Pérez‐Encabo may publish in the future.

Co-authorship network of co-authors of Alfonso Pérez‐Encabo

This figure shows the co-authorship network connecting the top 25 collaborators of Alfonso Pérez‐Encabo. A scholar is included among the top collaborators of Alfonso Pérez‐Encabo 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 Alfonso Pérez‐Encabo. Alfonso Pérez‐Encabo 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.
Meana, Clara, et al.. (2025). Phosphatidylcholine-bound palmitoleic acid: A bioactive key to unlocking macrophage anti-inflammatory functions. Biomedicine & Pharmacotherapy. 192. 118652–118652.
2.
López, Juan C., et al.. (2021). Decoding the Structure of Non-Proteinogenic Amino Acids: The Rotational Spectrum of Jet-Cooled Laser-Ablated Thioproline. Molecules. 26(24). 7585–7585. 4 indexed citations
3.
Astudillo, Alma M., et al.. (2020). Release of Anti-Inflammatory Palmitoleic Acid and Its Positional Isomers by Mouse Peritoneal Macrophages. Biomedicines. 8(11). 480–480. 35 indexed citations
4.
Barbero, Héctor, J.M. Martin-Alvarez, Alfonso Pérez‐Encabo, et al.. (2017). Copper Complexes in the Promotion of Aldol Addition to Pyridine-2-carboxaldehyde: Synthesis of Homo- and Heteroleptic Complexes and Stereoselective Double Aldol Addition. Inorganic Chemistry. 57(1). 264–276. 6 indexed citations
5.
6.
Maestro, Alicia, et al.. (2011). Studies on the Diastereoselective Intramolecular Pauson–Khand Reaction on Regioisomeric Chiral Perhydrobenzoxazines Derived from (–)‐8‐Aminomenthol. European Journal of Organic Chemistry. 2012(6). 1202–1208. 2 indexed citations
7.
Andrés, José M., Rafaël Pedrosa, & Alfonso Pérez‐Encabo. (2006). Diastereoselective syntheses of 2-amino propargyl alcohols. Chiral building blocks for enantiopure amino γ-lactones and 5-hydroxy-piperidinone derivatives. Tetrahedron Letters. 47(30). 5317–5320. 17 indexed citations
8.
Andrés, José M., Rafaël Pedrosa, Alfonso Pérez‐Encabo, & Marı́a Jesús Ramı́rez-Expósito. (2006). Diastereoselective synthesis of enantioenriched homopropargyl amino alcohols from α-dibenzylamino aldehydes and their use as chiral synthons. Tetrahedron. 62(33). 7783–7792. 3 indexed citations
9.
Pérez‐Encabo, Alfonso, et al.. (2001). Tautomerization tendencies of 2-acetylcycloalkanones, 2-acetyl-1,3-cycloalkanediones, and cyclic β-keto esters of five- and six-membered rings. Canadian Journal of Chemistry. 79(4). 448–454. 1 indexed citations
10.
11.
Andrés, José M., et al.. (2001). Diastereoselective synthesis of enantiopure γ-amino-β-hydroxy acids by Reformatsky reaction of chiral α-dibenzylamino aldehydes. Tetrahedron. 57(40). 8521–8530. 26 indexed citations
12.
Andrés, José M., et al.. (2000). A Simple Stereoselective Synthesis of Enantiopure 2-Substituted Pyrrolidines and Piperidines from Chiral (R)-Phenylglycinol-Derived Bicyclic 1,3-Oxazolidines. European Journal of Organic Chemistry. 2000(9). 1719–1726. 27 indexed citations
13.
Andrés, José M., Rafaël Pedrosa, & Alfonso Pérez‐Encabo. (2000). Synthesis of Chiral, Non-racemic Aldols from Chiral β-Hydroxy-Weinreb Amides Prepared by Enantioselective Reformatsky-like Reaction Induced by Chiral β-Aminoalcohols. Tetrahedron. 56(9). 1217–1223. 24 indexed citations
14.
15.
Andrés, José M., Yolanda Castro, Rafaël Pedrosa, & Alfonso Pérez‐Encabo. (1997). Enantioselective reformatsky reaction induced by chiral β-amino alcohols. Tetrahedron. 53(10). 3787–3794. 34 indexed citations
16.
Andrés, José M., M. Alejandra Martínez, Rafaël Pedrosa, & Alfonso Pérez‐Encabo. (1996). Synthesis of Chiral α,α-Difluoro-β-hydroxy Esters by Enantioselective Reformatsky Reaction. Synthesis. 1996(9). 1070–1072. 29 indexed citations
17.
Pérez‐Encabo, Alfonso, et al.. (1994). Oxidation of alkylthio substituted tricarbonyl(η6-arene)chromium(0) complexes to alkylsulfinyl substituted tricarbonyl(η6-arene)chromium(0) complexes. Journal of the Chemical Society Perkin Transactions 1. 629–642. 13 indexed citations
18.
Pérez‐Encabo, Alfonso, et al.. (1993). First synthesis of sulfinyl substituted tricarbonyl(η6-arene)chromium(0) complexes. Journal of the Chemical Society Chemical Communications. 1059–1062. 11 indexed citations
19.
Andrés, Celia, et al.. (1992). Stereoselective ring opening of chiral oxazolidines by reformatsky reagents: an enantioselective entry to β-amino esters.. Tetrahedron Letters. 33(20). 2895–2898. 26 indexed citations
20.

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