Ibrahim Ibnusaud

559 total citations
20 papers, 474 citations indexed

About

Ibrahim Ibnusaud is a scholar working on Organic Chemistry, Spectroscopy and Atomic and Molecular Physics, and Optics. According to data from OpenAlex, Ibrahim Ibnusaud has authored 20 papers receiving a total of 474 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Organic Chemistry, 6 papers in Spectroscopy and 4 papers in Atomic and Molecular Physics, and Optics. Recurrent topics in Ibrahim Ibnusaud's work include Asymmetric Synthesis and Catalysis (7 papers), Molecular spectroscopy and chirality (6 papers) and Chemical synthesis and alkaloids (5 papers). Ibrahim Ibnusaud is often cited by papers focused on Asymmetric Synthesis and Catalysis (7 papers), Molecular spectroscopy and chirality (6 papers) and Chemical synthesis and alkaloids (5 papers). Ibrahim Ibnusaud collaborates with scholars based in India, United States and Oman. Ibrahim Ibnusaud's co-authors include Thomas J. Colacot, Carin C. C. Johansson Seechurn, Prasad L. Polavarapu, Divya S. Nair, Giovanni Scalmani, Ganesh Shanmugam, Carmelo J. Rizzo, Jevgenij A. Raskatov, Bakthan Singaram and N. Sundaram and has published in prestigious journals such as The Journal of Organic Chemistry, Tetrahedron and The Journal of Physical Chemistry A.

In The Last Decade

Ibrahim Ibnusaud

20 papers receiving 467 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ibrahim Ibnusaud India 15 340 131 94 60 42 20 474
Ryan P. Pemberton United States 15 404 1.2× 54 0.4× 169 1.8× 77 1.3× 35 0.8× 25 618
Agata Suszczyńska Poland 8 140 0.4× 98 0.7× 143 1.5× 33 0.6× 47 1.1× 12 362
Markus Heubes Germany 10 313 0.9× 104 0.8× 64 0.7× 50 0.8× 18 0.4× 20 472
James Kallmerten United States 18 535 1.6× 79 0.6× 147 1.6× 33 0.6× 26 0.6× 43 673
József Tamás Hungary 13 291 0.9× 83 0.6× 134 1.4× 29 0.5× 28 0.7× 66 451
Juán Zinczuk Argentina 14 378 1.1× 112 0.9× 126 1.3× 57 0.9× 25 0.6× 56 601
Olga A. Мukhina United States 15 581 1.7× 156 1.2× 152 1.6× 14 0.2× 25 0.6× 36 744
Rubén Sánchez‐Obregón Mexico 14 326 1.0× 56 0.4× 112 1.2× 19 0.3× 14 0.3× 50 432
Takahisa Machiguchi Japan 16 548 1.6× 59 0.5× 167 1.8× 65 1.1× 73 1.7× 61 819
Osamu Kamo Japan 9 182 0.5× 94 0.7× 127 1.4× 22 0.4× 20 0.5× 14 354

Countries citing papers authored by Ibrahim Ibnusaud

Since Specialization
Citations

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

Fields of papers citing papers by Ibrahim Ibnusaud

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ibrahim Ibnusaud

This figure shows the co-authorship network connecting the top 25 collaborators of Ibrahim Ibnusaud. A scholar is included among the top collaborators of Ibrahim Ibnusaud 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 Ibrahim Ibnusaud. Ibrahim Ibnusaud 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.
Ibnusaud, Ibrahim, et al.. (2021). Cover Feature: Synthesis of Pyrrolo[2,1‐a]isoquinoline Class of Natural Product Crispine A (Eur. J. Org. Chem. 35/2021). European Journal of Organic Chemistry. 2021(35). 4896–4896. 2 indexed citations
2.
Ibnusaud, Ibrahim, et al.. (2021). Synthesis of Pyrrolo[2,1‐a]isoquinoline Class of Natural Product Crispine A. European Journal of Organic Chemistry. 2021(35). 4911–4926. 26 indexed citations
3.
Polavarapu, Prasad L., et al.. (2020). How important are the intermolecular hydrogen bonding interactions in methanol solvent for interpreting the chiroptical properties?. Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy. 247. 119094–119094. 16 indexed citations
4.
Singh, Vijay P., Ibrahim Ibnusaud, Shridhar R. Gadre, & Milind M. Deshmukh. (2020). Fragmentation method reveals a wide spectrum of intramolecular hydrogen bond energies in antioxidant natural products. New Journal of Chemistry. 44(15). 5841–5849. 18 indexed citations
5.
Nair, Divya S., et al.. (2020). Natural Product-Derived Chiral Pyrrolidine-2,5-diones, Their Molecular Structures and Conversion to Pharmacologically Important Skeletons. Journal of Natural Products. 83(7). 2178–2190. 19 indexed citations
6.
7.
Nair, Divya S., et al.. (2018). Stabilization of NaBH4 in Methanol Using a Catalytic Amount of NaOMe. Reduction of Esters and Lactones at Room Temperature without Solvent-Induced Loss of Hydride. The Journal of Organic Chemistry. 83(3). 1431–1440. 40 indexed citations
8.
Joseph, David, et al.. (2017). Capillary zone electrophorsis for the analysis of naturally occurring 2‐hydroxycitric acids and their lactones. Journal of Separation Science. 40(16). 3351–3357. 3 indexed citations
9.
Ibnusaud, Ibrahim, et al.. (2014). Palladium‐Catalyzed α‐Arylation Reactions in Total Synthesis. European Journal of Organic Chemistry. 2015(1). 38–49. 96 indexed citations
10.
Nair, Divya S. & Ibrahim Ibnusaud. (2014). Synthesis of enantiopure furo[2,3-b]pyrroles. Tetrahedron Letters. 55(42). 5822–5824. 3 indexed citations
11.
Polavarapu, Prasad L., et al.. (2012). Chiroptical Spectroscopy of Natural Products: Avoiding the Aggregation Effects of Chiral Carboxylic Acids. Journal of Natural Products. 75(8). 1441–1450. 23 indexed citations
12.
Ibnusaud, Ibrahim, et al.. (2012). Enantiomerically pure compounds related to chiral hydroxy acids derived from renewable resources. RSC Advances. 2(25). 9257–9257. 16 indexed citations
13.
Polavarapu, Prasad L., et al.. (2011). A Single Chiroptical Spectroscopic Method May Not Be Able To Establish the Absolute Configurations of Diastereomers: Dimethylesters of Hibiscus and Garcinia Acids. The Journal of Physical Chemistry A. 115(22). 5665–5673. 59 indexed citations
14.
Polavarapu, Prasad L., et al.. (2010). Importance of Solvation in Understanding the Chiroptical Spectra of Natural Products in Solution Phase: Garcinia Acid Dimethyl Ester. Journal of Natural Products. 74(3). 321–328. 23 indexed citations
15.
Ibnusaud, Ibrahim, et al.. (2007). Synthesis of enantiopure concave (+)-avenaciolide and (−)-canadensolide skeletons. Tetrahedron Letters. 48(46). 8209–8212. 9 indexed citations
16.
Nair, Mangalam S., et al.. (2006). Analogues of the Quararibea metabolite chiral enolic-γ-lactone from (2S,3S)- and (2S,3R)-tetrahydro-3-hydroxy-5-oxo-2,3-furandicarboxylic acids. Tetrahedron Letters. 47(45). 7957–7960. 3 indexed citations
17.
Ibnusaud, Ibrahim, et al.. (2003). Biologically interesting chiral 3,4-disubstituted pyrrolidines from optically active hydroxycitric acid lactones. Tetrahedron Letters. 44(6). 1247–1249. 31 indexed citations
18.
Ibnusaud, Ibrahim, et al.. (2002). Chiral γ-butyrolactones related to optically active 2-hydroxycitric acids. Tetrahedron. 58(24). 4887–4892. 27 indexed citations
19.
Ibnusaud, Ibrahim, E. J. Padma Malar, & N. Sundaram. (1990). Synthesis and Diels-Alder reaction of stable aryl free 1,3-diazabutadiene. Tetrahedron Letters. 31(50). 7357–7358. 15 indexed citations
20.
Ibnusaud, Ibrahim, et al.. (1986). Diels-alder cycloaddition reactions of 1,3-diazabutadienes with ketenes. Tetrahedron Letters. 27(48). 5875–5876. 30 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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