Suresh Pindi

810 total citations
14 papers, 714 citations indexed

About

Suresh Pindi is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, Suresh Pindi has authored 14 papers receiving a total of 714 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Organic Chemistry, 6 papers in Molecular Biology and 6 papers in Inorganic Chemistry. Recurrent topics in Suresh Pindi's work include Asymmetric Synthesis and Catalysis (9 papers), Chemical Synthesis and Analysis (6 papers) and Asymmetric Hydrogenation and Catalysis (5 papers). Suresh Pindi is often cited by papers focused on Asymmetric Synthesis and Catalysis (9 papers), Chemical Synthesis and Analysis (6 papers) and Asymmetric Hydrogenation and Catalysis (5 papers). Suresh Pindi collaborates with scholars based in United States and China. Suresh Pindi's co-authors include Guigen Li, Parminder Kaur, Walter J. Wever, Min Shi, Bo Jiang, Shu‐Jiang Tu, Trideep Rajale, Yin Wei, Fangle Hu and F. Dean Toste and has published in prestigious journals such as Journal of the American Chemical Society, Chemical Communications and Green Chemistry.

In The Last Decade

Suresh Pindi

14 papers receiving 697 citations

Peers

Suresh Pindi
Suresh Pindi
Citations per year, relative to Suresh Pindi Suresh Pindi (= 1×) peers Liangliang Song

Countries citing papers authored by Suresh Pindi

Since Specialization
Citations

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

Fields of papers citing papers by Suresh Pindi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Suresh Pindi

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

All Works

14 of 14 papers shown
1.
Rorrer, Julie E., Suresh Pindi, F. Dean Toste, & Alexis T. Bell. (2018). Effect of Alcohol Structure on the Kinetics of Etherification and Dehydration over Tungstated Zirconia. ChemSusChem. 11(18). 3104–3111. 32 indexed citations
2.
Niemeyer, Zachary L., Suresh Pindi, Cynthia Hong, et al.. (2017). Parameterization of Acyclic Diaminocarbene Ligands Applied to a Gold(I)-Catalyzed Enantioselective Tandem Rearrangement/Cyclization. Journal of the American Chemical Society. 139(37). 12943–12946. 83 indexed citations
3.
Pindi, Suresh, et al.. (2015). Asymmetric synthesis of homoallylic amines via 1,2-addition of Grignard reagent to aliphatic N-phosphonyl hemiaminal. Tetrahedron Letters. 57(5). 619–622. 9 indexed citations
4.
Pindi, Suresh, et al.. (2014). Asymmetric Carbamoyl Anion Additions to Chiral N-Phosphonyl Imines via the GAP Chemistry Process and Stereoselectivity Enrichments. The Journal of Organic Chemistry. 80(1). 447–452. 23 indexed citations
5.
Hu, Fangle, Yin Wei, Min Shi, Suresh Pindi, & Guigen Li. (2013). Asymmetric catalytic aza-Morita–Baylis–Hillman reaction for the synthesis of 3-substituted-3-aminooxindoles with chiral quaternary carbon centers. Organic & Biomolecular Chemistry. 11(12). 1921–1921. 94 indexed citations
6.
Pindi, Suresh, et al.. (2013). Design, Synthesis, and Applications of Chiral N-2-Phenyl-2-propyl Sulfinyl Imines for Group-Assisted Purification (GAP) Asymmetric Synthesis. The Journal of Organic Chemistry. 78(8). 4006–4012. 33 indexed citations
7.
Jiang, Bo, et al.. (2012). Efficient Domino Approaches to Multifunctionalized Fused Pyrroles and Dibenzo[b,e][1,4]diazepin-1-ones. Organic Letters. 14(3). 700–703. 76 indexed citations
8.
9.
Kaur, Parminder, Walter J. Wever, Suresh Pindi, et al.. (2011). The GAP chemistry for chiral N-phosphonyl imine-based Strecker reaction. Green Chemistry. 13(5). 1288–1288. 50 indexed citations
10.
Kattamuri, Padmanabha V., Teng Ai, Suresh Pindi, et al.. (2011). Asymmetric Synthesis of α-Amino-1,3-dithianes via Chiral N-Phosphonyl Imine-Based Umpolung Reaction Without Using Chromatography and Recrystallization. The Journal of Organic Chemistry. 76(8). 2792–2797. 35 indexed citations
11.
Kaur, Parminder, Suresh Pindi, Walter J. Wever, Trideep Rajale, & Guigen Li. (2010). Asymmetric catalytic Strecker reaction of N-phosphonyl imines with Et2AlCN using amino alcohols and BINOLs as catalysts. Chemical Communications. 46(24). 4330–4330. 66 indexed citations
12.
Pindi, Suresh, et al.. (2010). N‐Phosphinyl Imine Chemistry (I): Design and Synthesis of Novel N‐Phosphinyl Imines and their Application to Asymmetric aza‐Henry Reaction. Chemical Biology & Drug Design. 77(1). 20–29. 40 indexed citations
13.
Ai, Teng, Suresh Pindi, Padmanabha V. Kattamuri, & Guigen Li. (2010). Chiral N-phosphonyl imine chemistry: asymmetric additions of glycine enolate to diphenyl diamine-based phosphonyl imines. Science China Chemistry. 53(1). 125–129. 14 indexed citations
14.
Kaur, Parminder, Suresh Pindi, Walter J. Wever, Trideep Rajale, & Guigen Li. (2010). Asymmetric Catalytic N-Phosphonyl Imine Chemistry: The Use of Primary Free Amino Acids and Et2AlCN for Asymmetric Catalytic Strecker Reaction. The Journal of Organic Chemistry. 75(15). 5144–5150. 60 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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