Manjula Alla

996 total citations
52 papers, 832 citations indexed

About

Manjula Alla is a scholar working on Organic Chemistry, Molecular Biology and Spectroscopy. According to data from OpenAlex, Manjula Alla has authored 52 papers receiving a total of 832 indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Organic Chemistry, 10 papers in Molecular Biology and 7 papers in Spectroscopy. Recurrent topics in Manjula Alla's work include Synthesis and biological activity (15 papers), Synthesis and Biological Evaluation (11 papers) and Multicomponent Synthesis of Heterocycles (9 papers). Manjula Alla is often cited by papers focused on Synthesis and biological activity (15 papers), Synthesis and Biological Evaluation (11 papers) and Multicomponent Synthesis of Heterocycles (9 papers). Manjula Alla collaborates with scholars based in India. Manjula Alla's co-authors include B. Vittal Rao, Vittal Rao Bommena, Balasubramanian Sridhar, Nishant Jain, A. Addlagatta, Sowjanya Polepalli, M. NAGARAJAN, M. Nagarajan, Jagadeesh Babu Nanubolu and M.S. Shailaja and has published in prestigious journals such as The Journal of Organic Chemistry, Tetrahedron and RSC Advances.

In The Last Decade

Manjula Alla

50 papers receiving 812 citations

Peers

Manjula Alla

PHARM

SPECT

Nikolay Yu. Gorobets Ukraine

I. Wolska Poland

Mahantesha Basanagouda India

И. В. Украинец Ukraine

Jarosław Sączewski Poland

Maralinganadoddi P. Sadashiva India

Koushik Das Sarma India

Timothy T. Curran United States

C. Kırılmış Türkiye

Kailash G. Bothara India

Nikolay Yu. Gorobets Ukraine

Manjula Alla

909 ×1.2

206 ×1.5

99 ×1.1

PHARM

33 ×0.5

SPECT

62 ×1.1

Citations per year, relative to Manjula Alla Manjula Alla (= 1×) peers Nikolay Yu. Gorobets

Countries citing papers authored by Manjula Alla

Since Specialization

Citations

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

Fields of papers citing papers by Manjula Alla

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manjula Alla

This figure shows the co-authorship network connecting the top 25 collaborators of Manjula Alla. A scholar is included among the top collaborators of Manjula Alla 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 Manjula Alla. Manjula Alla 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

Alla, Manjula, et al.. (2021). Exo-selective intermolecular Diels–Alder reaction by PyrI4 and AbnU on non-natural substrates. Communications Chemistry. 4(1). 113–113. 5 indexed citations

Alla, Manjula, et al.. (2020). CuI/I ₂ ‐Catalyzed Concise Synthesis of Substituted 6‐Aminoisoquinolinoquinazoline Carboxylates from Anthranilamide. ChemistrySelect. 5(37). 11685–11689. 3 indexed citations

Nanubolu, Jagadeesh Babu, et al.. (2018). Copper-Catalyzed Domino Addition, Hydroamination, and Cyclization: A Multicomponent Approach to Spiro Oxazolidinone Derivatives. The Journal of Organic Chemistry. 83(24). 15186–15194. 18 indexed citations

Kotapalli, Sudha Sravanti, et al.. (2017). Ring Functionalization and Molecular Hybridization of Quinolinyl Pyrazole: Design, Synthesis and Antimycobacterial Activity. ChemistrySelect. 2(22). 6529–6534. 7 indexed citations

Alla, Manjula, et al.. (2016). Synthesis of Tröger’s base bis(α-aminophosphonate) derivatives. ARKIVOC. 2016(4). 246–260. 2 indexed citations

Alla, Manjula, et al.. (2015). Synthesis and antiproliferative activity of imidazo[1,2-a]pyrimidine Mannich bases. European Journal of Medicinal Chemistry. 100. 18–23. 60 indexed citations

Alla, Manjula, et al.. (2015). Solvent-free one-pot synthesis of polysubstituted tetrahydropyrimidines and their antioxidant and antimicrobial properties. Research on Chemical Intermediates. 42(2). 923–937. 4 indexed citations

Alla, Manjula, et al.. (2015). Highly functionalized tetrahydropyridines are cytotoxic and selective inhibitors of human puromycin sensitive aminopeptidase. European Journal of Medicinal Chemistry. 106. 26–33. 12 indexed citations

Alla, Manjula, et al.. (2014). “One-pot” access to dihydrofurans via tandem oxidative difunctionalization and ring contraction of aminopyrans. Organic & Biomolecular Chemistry. 12(25). 4412–4412. 5 indexed citations

10.

Alla, Manjula, et al.. (2014). Discovery of Tröger's base analogues as selective inhibitors against human breast cancer cell line: Design, synthesis and cytotoxic evaluation. European Journal of Medicinal Chemistry. 86. 39–47. 14 indexed citations

11.

Alla, Manjula, et al.. (2013). Design, diversity-oriented synthesis and structure activity relationship studies of quinolinyl heterocycles as antimycobacterial agents. European Journal of Medicinal Chemistry. 70. 536–547. 30 indexed citations

12.

Alla, Manjula, et al.. (2013). Synthesis and biological screening of 5-(alkyl(1H-indol-3-yl))-2-(substituted)-1,3,4-oxadiazoles as antiproliferative and anti-inflammatory agents. European Journal of Medicinal Chemistry. 66. 91–100. 40 indexed citations

13.

Alla, Manjula, et al.. (2012). Eco-friendly synthesis and biological evaluation of substituted pyrano[2,3-c]pyrazoles. Bioorganic & Medicinal Chemistry Letters. 22(16). 5272–5278. 172 indexed citations

14.

Alla, Manjula, et al.. (2011). ChemInform Abstract: Synthesis of Novel 3,5‐Disubstituted‐4,5‐dihydroisoxazoles and 3,4,5‐Trisubstituted Isoxazoles and Their Biological Activity.. ChemInform. 42(22). 1 indexed citations

15.

Alla, Manjula, et al.. (2011). Regioselective Synthesis of Dimethylamino‐ or Arylalkylamino‐‘‘Crowned” Tröger's Base Analogues Under Vilsmeier–Haack Conditions. European Journal of Organic Chemistry. 2012(2). 312–319. 8 indexed citations

16.

Shailaja, M.S., et al.. (2010). Synthesis and biological activity of novel 2,5-disubstituted-1,3,4-oxadiazoles. Indian Journal of Chemistry Section B-organic Chemistry Including Medicinal Chemistry. 49(8). 1088–1097. 12 indexed citations

17.

Alla, Manjula, et al.. (2010). Three component one pot synthesis of β-amino ketones mediated by . (bromodimethyl)sulfonium bromide. Indian Journal of Chemistry Section B-organic Chemistry Including Medicinal Chemistry. 49(4). 482–488. 2 indexed citations

18.

Alla, Manjula, et al.. (2010). Structure activity relationship studies of imidazo[1,2-a]pyrazine derivatives against cancer cell lines. European Journal of Medicinal Chemistry. 45(11). 5208–5216. 53 indexed citations

19.

Alla, Manjula, et al.. (2007). (Bromodimethyl)sulfonium bromide mediated Michael addition of thiols to α, β-unsaturated ketones. Journal of Sulfur Chemistry. 28(1). 31–38. 5 indexed citations

20.

Alla, Manjula, et al.. (2003). Oxidative Deoximation with Catalytic Sodium Tungstate. Synthetic Communications. 33(19). 3455–3459. 4 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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