Egle M. Beccalli

4.4k total citations · 1 hit paper
133 papers, 3.8k citations indexed

About

Egle M. Beccalli is a scholar working on Organic Chemistry, Molecular Biology and Pharmaceutical Science. According to data from OpenAlex, Egle M. Beccalli has authored 133 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 129 papers in Organic Chemistry, 19 papers in Molecular Biology and 13 papers in Pharmaceutical Science. Recurrent topics in Egle M. Beccalli's work include Catalytic C–H Functionalization Methods (54 papers), Synthesis and Biological Evaluation (28 papers) and Synthesis and Reactions of Organic Compounds (28 papers). Egle M. Beccalli is often cited by papers focused on Catalytic C–H Functionalization Methods (54 papers), Synthesis and Biological Evaluation (28 papers) and Synthesis and Reactions of Organic Compounds (28 papers). Egle M. Beccalli collaborates with scholars based in Italy, France and Germany. Egle M. Beccalli's co-authors include Gianluigi Broggini, Michela Martinelli, Silvia Sottocornola, A. MARCHESINI, Elena Borsini, Tullio Pilati, Maria Luisa Gelmi, Giorgio Abbiati, Silvia Gazzola and Francesca Clerici and has published in prestigious journals such as Chemical Reviews, Angewandte Chemie International Edition and Inorganic Chemistry.

In The Last Decade

Egle M. Beccalli

131 papers receiving 3.7k citations

Hit Papers

1 papers align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

C−C, C−O, C−N Bond Formation on sp² Carbon by Pd(II)-Catalyzed Reactions Involving Oxidant Agents

2007 1.1k citations Egle M. Beccalli, Gianluigi Broggini et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Egle M. Beccalli Italy	30	3.6k	489	457	116	110	133	3.8k
Gianluigi Broggini Italy	32	3.8k 1.1×	498 1.0×	516 1.1×	126 1.1×	93 0.8×	153	4.0k
Carlos Saá Spain	37	3.7k 1.0×	450 0.9×	388 0.8×	111 1.0×	81 0.7×	116	3.8k
Yongwen Jiang China	26	3.4k 1.0×	459 0.9×	471 1.0×	127 1.1×	241 2.2×	63	3.7k
Raúl SanMartı́n Spain	40	3.6k 1.0×	382 0.8×	353 0.8×	96 0.8×	214 1.9×	112	3.8k
Hirokazu Urabe Japan	34	3.4k 0.9×	583 1.2×	378 0.8×	152 1.3×	96 0.9×	126	3.5k
Fabio Marinelli Italy	41	4.6k 1.3×	503 1.0×	553 1.2×	110 0.9×	139 1.3×	145	4.8k
Krishna Nand Singh India	31	3.3k 0.9×	292 0.6×	545 1.2×	110 0.9×	118 1.1×	172	3.5k
James P. Stambuli United States	25	3.6k 1.0×	747 1.5×	391 0.9×	125 1.1×	156 1.4×	39	3.8k
Georg Manolikakes Germany	36	3.5k 1.0×	341 0.7×	422 0.9×	162 1.4×	103 0.9×	95	3.8k
Itaru Nakamura Japan	39	5.9k 1.7×	592 1.2×	330 0.7×	160 1.4×	119 1.1×	126	6.1k

Countries citing papers authored by Egle M. Beccalli

Since Specialization

Citations

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

Fields of papers citing papers by Egle M. Beccalli

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Egle M. Beccalli. 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 Egle M. Beccalli. The network helps show where Egle M. Beccalli may publish in the future.

Co-authorship network of co-authors of Egle M. Beccalli

This figure shows the co-authorship network connecting the top 25 collaborators of Egle M. Beccalli. A scholar is included among the top collaborators of Egle M. Beccalli 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 Egle M. Beccalli. Egle M. Beccalli is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Foschi, Francesca, et al.. (2023). Copper-Catalyzed/Hypervalent Iodine-Mediated Functionalization of Unactivated Compounds. Catalysts. 13(9). 1243–1243. 6 indexed citations

Molteni, L., et al.. (2023). Methanol as a C1 Source for the Synthesis of 1,3‐Polyheterocyclic Systems. European Journal of Organic Chemistry. 26(48). 5 indexed citations

Molteni, L., et al.. (2022). Non-Decarboxylative Ruthenium-Catalyzed Rearrangement of 4-Alkylidene-isoxazol-5-ones to Pyrazole- and Isoxazole-4-carboxylic Acids. Organic Letters. 24(16). 3092–3096. 11 indexed citations

Molteni, L., Egle M. Beccalli, Donatella Nava, et al.. (2022). Direct Synthesis of Fluorescent Oxazolo-phenoxazines by Copper-Catalyzed/Hypervalent Iodine(III)-Mediated Dimerization/Cyclization of 2-Benzylamino-phenols. The Journal of Organic Chemistry. 87(2). 1032–1042. 12 indexed citations

Oble, Julie, Francesca Foschi, Egle M. Beccalli, et al.. (2022). Acid-mediated decarboxylative C–H coupling between arenes and O-allyl carbamates. Organic Chemistry Frontiers. 9(6). 1711–1718. 10 indexed citations

Molteni, L., et al.. (2022). Ruthenium‐Catalyzed Decarboxylative Rearrangement of 4‐Alkenyl‐isoxazol‐5‐ones to Pyrrole Derivatives. European Journal of Organic Chemistry. 2022(25). 10 indexed citations

Giofrè, Sabrina, Manfred Keller, Leonardo Lo Presti, Egle M. Beccalli, & L. Molteni. (2021). Switchable Oxidative Reactions of N-allyl-2-Aminophenols: Palladium-Catalyzed Alkoxyacyloxylation vs an Intramolecular Diels–Alder Reaction. Organic Letters. 23(20). 7698–7702. 9 indexed citations

Foschi, Francesca, Julie Oble, Leonardo Lo Presti, et al.. (2020). Intramolecular Aminoazidation of Unactivated Terminal Alkenes by Palladium-Catalyzed Reactions with Hydrogen Peroxide as the Oxidant. Organic Letters. 22(4). 1402–1406. 35 indexed citations

Bucci, Raffaella, Alessandro Contini, Francesca Clerici, et al.. (2019). Fluoro-Aryl Substituted α,β2,3-Peptides in the Development of Foldameric Antiparallel β-Sheets: A Conformational Study. Frontiers in Chemistry. 7. 192–192. 18 indexed citations

10.

Christodoulou, Michael S., Ferdinando Nicoletti, Katia Mangano, et al.. (2019). Novel 3,3-disubstituted oxindole derivatives. Synthesis and evaluation of the anti-proliferative activity. Bioorganic & Medicinal Chemistry Letters. 30(2). 126845–126845. 22 indexed citations

11.

Gazzola, Silvia, et al.. (2016). Palladium‐Catalysed Carbo‐ and Hydroamination of Allenyl Ethers and Aminoallenes: Available Entry to Nitrogen‐Containing Benzo‐Fused Rings. European Journal of Organic Chemistry. 2016(26). 4534–4544. 12 indexed citations

12.

Broggini, Gianluigi, et al.. (2015). Ruthenium‐Catalyzed Hydroamination of Aminoallenes: an Approach to Vinyl Substituted Heterocycles. Advanced Synthesis & Catalysis. 357(4). 677–682. 16 indexed citations

13.

Beccalli, Egle M., Elena Borsini, Stefano Brenna, et al.. (2009). σ‐Alkylpalladium Intermediates in Intramolecular Heck Reactions:Isolation and Catalytic Activity. Chemistry - A European Journal. 16(5). 1670–1678. 37 indexed citations

14.

Beccalli, Egle M., Gianluigi Broggini, Michela Martinelli, & Giuseppe Paladino. (2004). Pd-catalyzed intramolecular cyclization of pyrrolo-2-carboxamides: regiodivergent routes to pyrrolo-pyrazines and pyrrolo-pyridines. Tetrahedron. 61(5). 1077–1082. 38 indexed citations

15.

Beccalli, Egle M., et al.. (2002). A Valuable Approach to Enantiopure Partially Saturated Pyrrolo- and Indolo[1,2-a]indoles by Intramolecular Nitrone Cycloadditions to the Cyclohexene Ring. European Journal of Organic Chemistry. 2002(13). 2080–2080. 16 indexed citations

16.

Beccalli, Egle M., Francesca Clerici, & Maria Luisa Gelmi. (1999). 5(4H)-oxazolones. Part XIII. A new synthesis of 4-ylidene-5(4H)-oxazolones by the Stille reaction. Tetrahedron. 55(3). 781–786. 17 indexed citations

17.

Beccalli, Egle M., A. MARCHESINI, & Tullio Pilati. (1996). Diels-Alder reactions of (Z)-ethyl 3-[(1-ethoxycarbonyloxy-2-methoxy)ethenyl]-2-(ethoxycarbonyloxy)indole-1-carboxylate. Synthesis of the carbazole alkaloid Carbazomycin B. Tetrahedron. 52(8). 3029–3036. 28 indexed citations

18.

Beccalli, Egle M. & A. MARCHESINI. (1995). SYNTHESIS OF 3-VINYLINDOLES FROM 3-ALKYLIDENEINDOL-2(3H)-ONES. Organic Preparations and Procedures International. 27(1). 113–117. 2 indexed citations

19.

Ardizzoia, G. Attilio, et al.. (1992). Co-ordinative versatility of the dmcpz ligand (Hdmcpz = 3,5-dimethoxycarbonylpyrazole) in copper compounds. Synthesis, characterization and crystal structures of [Cu(dmcpz)2(py)2] and [Cu3(dmcpz)6](py = pyridine). Journal of the Chemical Society Dalton Transactions. 2715–2715. 11 indexed citations

20.

Beccalli, Egle M., A. MARCHESINI, & F. Sannicolò. (1984). Reaction path of aqueous sodium hydroxide induced ring opening of 4-bromo-3,4-diphenyl-2-isoxazolin-2-one. The Journal of Organic Chemistry. 49(11). 2071–2073. 1 indexed citations

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