Amparo Sanz‐Marco

1.1k total citations
47 papers, 957 citations indexed

About

Amparo Sanz‐Marco is a scholar working on Organic Chemistry, Pharmaceutical Science and Inorganic Chemistry. According to data from OpenAlex, Amparo Sanz‐Marco has authored 47 papers receiving a total of 957 indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Organic Chemistry, 14 papers in Pharmaceutical Science and 10 papers in Inorganic Chemistry. Recurrent topics in Amparo Sanz‐Marco's work include Asymmetric Synthesis and Catalysis (21 papers), Catalytic C–H Functionalization Methods (14 papers) and Cyclopropane Reaction Mechanisms (14 papers). Amparo Sanz‐Marco is often cited by papers focused on Asymmetric Synthesis and Catalysis (21 papers), Catalytic C–H Functionalization Methods (14 papers) and Cyclopropane Reaction Mechanisms (14 papers). Amparo Sanz‐Marco collaborates with scholars based in Spain, Sweden and Portugal. Amparo Sanz‐Marco's co-authors include Gonzalo Blay, José R. Pedro, Belén Martı́n-Matute, Carlos Vila, M. Carmen Muñoz, Sergio Carrasco, James P. Morken, Liang Zhang, Ana Vázquez‐Romero and Andrea García‐Ortiz and has published in prestigious journals such as Journal of the American Chemical Society, Nature Communications and Chemical Communications.

In The Last Decade

Amparo Sanz‐Marco

46 papers receiving 947 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Amparo Sanz‐Marco Spain 19 836 296 180 136 52 47 957
Yingguang Zhu China 20 1.7k 2.0× 311 1.1× 143 0.8× 125 0.9× 123 2.4× 57 1.8k
Li‐Jie Cheng China 16 962 1.2× 273 0.9× 95 0.5× 78 0.6× 38 0.7× 28 1.0k
Dayun Huang China 22 1.3k 1.5× 125 0.4× 115 0.6× 160 1.2× 38 0.7× 49 1.4k
Christopher J. Teskey Germany 18 1.1k 1.4× 315 1.1× 133 0.7× 150 1.1× 45 0.9× 39 1.2k
Muliang Zhang China 24 1.5k 1.8× 234 0.8× 397 2.2× 140 1.0× 65 1.3× 34 1.6k
Boris Gášpár Switzerland 8 941 1.1× 226 0.8× 73 0.4× 134 1.0× 39 0.8× 12 1.0k
Luqing Lin China 17 1.2k 1.4× 391 1.3× 55 0.3× 87 0.6× 39 0.8× 32 1.2k
Jian Lei China 15 678 0.8× 117 0.4× 69 0.4× 92 0.7× 41 0.8× 33 763
Guangying Tan China 20 1.1k 1.3× 159 0.5× 81 0.5× 61 0.4× 92 1.8× 29 1.2k

Countries citing papers authored by Amparo Sanz‐Marco

Since Specialization
Citations

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

Fields of papers citing papers by Amparo Sanz‐Marco

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Amparo Sanz‐Marco. 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 Amparo Sanz‐Marco. The network helps show where Amparo Sanz‐Marco may publish in the future.

Co-authorship network of co-authors of Amparo Sanz‐Marco

This figure shows the co-authorship network connecting the top 25 collaborators of Amparo Sanz‐Marco. A scholar is included among the top collaborators of Amparo Sanz‐Marco 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 Amparo Sanz‐Marco. Amparo Sanz‐Marco 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.
Blay, Gonzalo, Alicia Monleón, Marc Montesinos‐Magraner, Amparo Sanz‐Marco, & Carlos Vila. (2024). Asymmetric electrophilic functionalization of amino-substituted heteroaromatic compounds: a convenient tool for the enantioselective synthesis of nitrogen heterocycles. Chemical Communications. 60(85). 12270–12286. 4 indexed citations
2.
Sanz‐Marco, Amparo, et al.. (2024). Organocatalytic Diastereo‐ and Enantioselective Michael Addition of α‐Aryl Isocyanoacetates to Aurone‐Derived Azadienes. European Journal of Organic Chemistry. 27(31). 2 indexed citations
3.
4.
Carrasco, Sergio, et al.. (2023). One-step microwave-assisted synthesis of amino-functionalized chromium(III) terephthalate MIL-101-NH2. Materials Today Chemistry. 31. 101618–101618. 13 indexed citations
5.
Portillo, Eduardo, et al.. (2023). Enantioselective construction of quaternary stereocenters via organocatalytic arylation of isoxazolin-5-ones with o-quinone diimides. Organic Chemistry Frontiers. 10(24). 6081–6086. 8 indexed citations
6.
Sanz‐Marco, Amparo, et al.. (2022). Organocatalytic enantioselective Mannich reaction of isoxazol-5(4H)-ones to isatin-derived ketimines. Organic & Biomolecular Chemistry. 20(43). 8395–8399. 6 indexed citations
7.
Carrasco, Sergio, et al.. (2021). Selective Synthesis of Imines by Photo-Oxidative Amine Cross-Condensation Catalyzed by PCN-222(Pd). ACS Sustainable Chemistry & Engineering. 9(43). 14405–14415. 22 indexed citations
8.
Sheikhi, Ehsan, Amparo Sanz‐Marco, Carlos Vila, et al.. (2021). Enantioselective Addition of Sodium Bisulfite to Nitroalkenes. A Convenient Approach to Chiral Sulfonic Acids. European Journal of Organic Chemistry. 2021(37). 5284–5287. 4 indexed citations
9.
Sanz‐Marco, Amparo, et al.. (2021). Asymmetric Organocatalytic Synthesis of aza‐Spirocyclic Compounds from Isothiocyanates and Isocyanides. European Journal of Organic Chemistry. 2021(16). 2268–2284. 18 indexed citations
10.
Li, Man, Amparo Sanz‐Marco, Binh Khanh, et al.. (2020). Unraveling the Mechanism of the IrIII‐Catalyzed Regiospecific Synthesis of α‐Chlorocarbonyl Compounds from Allylic Alcohols. Chemistry - A European Journal. 26(65). 14978–14986. 10 indexed citations
11.
Sanz‐Marco, Amparo, et al.. (2020). Stereospecific Isomerization of Allylic Halides via Ion Pairs with Induced Noncovalent Chirality. Organic Letters. 22(11). 4123–4128. 18 indexed citations
12.
Blay, Gonzalo, et al.. (2020). Enantioselective zinc-mediated conjugate alkynylation of saccharin-derived 1-aza-butadienes. Chemical Communications. 56(66). 9461–9464. 3 indexed citations
13.
Carrasco, Sergio, et al.. (2019). Aerobic Homocoupling of Arylboronic Acids Catalyzed by Regenerable Pd(II)@MIL‐88B‐NH2(Cr). ChemCatChem. 11(16). 3933–3940. 12 indexed citations
14.
Molleti, Nagaraju, et al.. (2019). Base-Catalyzed [1,n]-Proton Shifts in Conjugated Polyenyl Alcohols and Ethers. ACS Catalysis. 9(10). 9134–9139. 20 indexed citations
15.
Sanz‐Marco, Amparo, et al.. (2019). An umpolung strategy to react catalytic enols with nucleophiles. Nature Communications. 10(1). 5244–5244. 26 indexed citations
16.
Blay, Gonzalo, et al.. (2019). Catalytic Diastereo- and Enantioselective Synthesis of 2-Imidazolinones. Organic Letters. 21(11). 4063–4066. 19 indexed citations
17.
Sanz‐Marco, Amparo, et al.. (2018). Selective Synthesis of Unsymmetrical Aliphatic Acyloins through Oxidation of Iridium Enolates. Chemistry - A European Journal. 24(45). 11564–11567. 10 indexed citations
18.
Blay, Gonzalo, et al.. (2018). Enantioselective synthesis of chiral oxazolines from unactivated ketones and isocyanoacetate esters by synergistic silver/organocatalysis. Chemical Communications. 54(23). 2862–2865. 28 indexed citations
19.
Sanz‐Marco, Amparo, et al.. (2017). Base- and Additive-Free Ir-Catalyzed ortho-Iodination of Benzoic Acids: Scope and Mechanistic Investigations. ACS Catalysis. 8(2). 920–925. 47 indexed citations
20.
Sanz‐Marco, Amparo, Gonzalo Blay, M. Carmen Muñoz, & José R. Pedro. (2016). Catalytic Enantioselective Conjugate Alkynylation of α,β‐Unsaturated 1,1,1‐Trifluoromethyl Ketones with Terminal Alkynes. Chemistry - A European Journal. 22(29). 10057–10064. 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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