Mouhamad Jida

553 total citations
28 papers, 426 citations indexed

About

Mouhamad Jida is a scholar working on Organic Chemistry, Molecular Biology and Oncology. According to data from OpenAlex, Mouhamad Jida has authored 28 papers receiving a total of 426 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Organic Chemistry, 15 papers in Molecular Biology and 4 papers in Oncology. Recurrent topics in Mouhamad Jida's work include Chemical Synthesis and Analysis (14 papers), Multicomponent Synthesis of Heterocycles (11 papers) and Synthetic Organic Chemistry Methods (8 papers). Mouhamad Jida is often cited by papers focused on Chemical Synthesis and Analysis (14 papers), Multicomponent Synthesis of Heterocycles (11 papers) and Synthetic Organic Chemistry Methods (8 papers). Mouhamad Jida collaborates with scholars based in France, Belgium and Poland. Mouhamad Jida's co-authors include Benoît Déprez, Steven Ballet, Rebecca Deprez‐Poulain, Guillaume Laconde, Dirk Tourwé, Mohamad Soueidan, Francine Agbossou‐Niedercorn, Jean Ollivier, Lydie Pélinski and Thomas Barlow and has published in prestigious journals such as Chemical Communications, Green Chemistry and Molecules.

In The Last Decade

Mouhamad Jida

28 papers receiving 410 citations

Peers

Mouhamad Jida
Sudharshan Madapa India
Silvia E. Ası́s Argentina
Shahnawaz Khan India
Garima Verma India
Woongki Kim United States
Gitte Van Baelen Belgium
Fatma E. Goda Egypt
Sharba Tasneem India
Rubén M. Carballo Mexico
Stanley N. S. Vasconcelos Brazil
Sudharshan Madapa India
Mouhamad Jida
Citations per year, relative to Mouhamad Jida Mouhamad Jida (= 1×) peers Sudharshan Madapa

Countries citing papers authored by Mouhamad Jida

Since Specialization
Citations

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

Fields of papers citing papers by Mouhamad Jida

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mouhamad Jida

This figure shows the co-authorship network connecting the top 25 collaborators of Mouhamad Jida. A scholar is included among the top collaborators of Mouhamad Jida 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 Mouhamad Jida. Mouhamad Jida 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.
Jida, Mouhamad & Steven Ballet. (2018). An Efficient One‐Pot Synthesis of Chiral N‐Protected 3‐Substituted (Diketo)piperazines via Ugi‐4CR/De‐Boc/Cyclization Process. ChemistrySelect. 3(4). 1027–1031. 8 indexed citations
2.
Maes, Bert U. W., et al.. (2018). Rapid construction of substituted 3-amino-1,5-benzothiazepin-4(5H)-one dipeptide scaffolds through an Ugi-4CR – Ullmann cross-coupling sequence. Organic & Biomolecular Chemistry. 16(8). 1242–1246. 6 indexed citations
3.
Jida, Mouhamad, Tobias Müller, Michael Lanzer, et al.. (2017). Pharmacomodulation of the Antimalarial Plasmodione: Synthesis of Biaryl- and N-Arylalkylamine Analogues, Antimalarial Activities and Physicochemical Properties. Molecules. 22(1). 161–161. 9 indexed citations
4.
Barlow, Thomas, Mouhamad Jida, Karel Guillemyn, et al.. (2016). Efficient one-pot synthesis of amino-benzotriazolodiazocinone scaffolds via catalyst-free tandem Ugi–Huisgen reactions. Organic & Biomolecular Chemistry. 14(20). 4669–4677. 13 indexed citations
5.
Jida, Mouhamad, et al.. (2016). A Redox-Active Fluorescent pH Indicator for Detecting Plasmodium falciparum Strains with Reduced Responsiveness to Quinoline Antimalarial Drugs. ACS Infectious Diseases. 3(2). 119–131. 7 indexed citations
6.
Jida, Mouhamad, et al.. (2016). A Platform of Regioselective Methodologies to Access Polysubstituted 2‐Methyl‐1,4‐naphthoquinone Derivatives: Scope and Limitations. European Journal of Organic Chemistry. 2016(11). 1982–1993. 21 indexed citations
7.
8.
Jida, Mouhamad, Dirk Tourwé, & Steven Ballet. (2014). Highly stereoselective one-pot construction of trisubstituted tetrahydro-β-carboline-fused diketopiperazines: a synthetic route towards cialis analogues. RSC Advances. 4(72). 38159–38163. 20 indexed citations
9.
Barlow, Thomas, Mouhamad Jida, Dirk Tourwé, & Steven Ballet. (2014). Efficient synthesis of conformationally constrained, amino-triazoloazepinone-containing di- and tripeptides via a one-pot Ugi–Huisgen tandem reaction. Organic & Biomolecular Chemistry. 12(36). 6986–6989. 23 indexed citations
10.
Jida, Mouhamad, Cecilia Betti, Peter W. Schiller, Dirk Tourwé, & Steven Ballet. (2014). One-Pot Isomerization–Cross Metathesis–Reduction (ICMR) Synthesis of Lipophilic Tetrapeptides. ACS Combinatorial Science. 16(7). 342–351. 8 indexed citations
11.
Jida, Mouhamad, Cecilia Betti, Z. Urbańczyk-Lipkowska, Dirk Tourwé, & Steven Ballet. (2013). Highly Diastereoselective Synthesis of 1-Carbamoyl-4-aminoindoloazepinone Derivatives via the Ugi Reaction. Organic Letters. 15(22). 5866–5869. 22 indexed citations
12.
Jida, Mouhamad, Guillaume Laconde, Mohamad Soueidan, et al.. (2012). Stereoselective synthesis of enantiopure N-protected-3-arylpiperazines from keto-esters. Tetrahedron Letters. 53(39). 5215–5218. 6 indexed citations
13.
Jida, Mouhamad & Benoît Déprez. (2012). Friedländer synthesis of polysubstituted quinolines and naphthyridines promoted by propylphosphonic anhydride (T3P®) under mild conditions. New Journal of Chemistry. 36(4). 869–869. 28 indexed citations
14.
Jida, Mouhamad, Mohamad Soueidan, Benoît Déprez, Guillaume Laconde, & Rebecca Deprez‐Poulain. (2012). Racemic and diastereoselective construction of indole alkaloids under solvent- and catalyst-free microwave-assisted Pictet–Spengler condensation. Green Chemistry. 14(4). 909–909. 28 indexed citations
15.
Soueidan, Mohamad, Mouhamad Jida, Till Bousquet, Francine Agbossou‐Niedercorn, & Lydie Pélinski. (2011). Efficient access to new chiral ferrocenyl γ-lactams from amino alcohols. New Journal of Chemistry. 35(5). 991–991. 1 indexed citations
16.
Ollivier, Jean, et al.. (2010). Titanium-Mediated Cyclopropanation on Diesters: Mechanistic Study on the Dramatic Effects of Selected Parameters. Synlett. 2010(11). 1627–1630. 1 indexed citations
17.
Jida, Mouhamad, Rebecca Deprez‐Poulain, Pascal Roussel, et al.. (2010). Solvent-free microwave-assisted Meyers’ lactamization. Green Chemistry. 12(6). 961–961. 28 indexed citations
18.
Jida, Mouhamad, et al.. (2010). Synthesis of five- and six-membered lactams via solvent-free microwave Ugi reaction. Tetrahedron Letters. 51(39). 5109–5111. 26 indexed citations
19.
Jida, Mouhamad, et al.. (2010). Ugi reaction for the synthesis of 4-aminopiperidine-4-carboxylic acid derivatives. Application to the synthesis of carfentanil and remifentanil. Tetrahedron Letters. 51(22). 2983–2985. 39 indexed citations
20.

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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