Christopher C. Nawrat

1.7k total citations
26 papers, 821 citations indexed

About

Christopher C. Nawrat is a scholar working on Organic Chemistry, Molecular Biology and Toxicology. According to data from OpenAlex, Christopher C. Nawrat has authored 26 papers receiving a total of 821 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Organic Chemistry, 6 papers in Molecular Biology and 4 papers in Toxicology. Recurrent topics in Christopher C. Nawrat's work include Bioactive Compounds and Antitumor Agents (4 papers), Chemical synthesis and alkaloids (4 papers) and Carbohydrate Chemistry and Synthesis (3 papers). Christopher C. Nawrat is often cited by papers focused on Bioactive Compounds and Antitumor Agents (4 papers), Chemical synthesis and alkaloids (4 papers) and Carbohydrate Chemistry and Synthesis (3 papers). Christopher C. Nawrat collaborates with scholars based in United Kingdom, United States and Spain. Christopher C. Nawrat's co-authors include Christopher J. Moody, Christopher R. Jamison, Yuriy Slutskyy, David W. C. MacMillan, Larry E. Overman, William Lewis, Russell R. A. Kitson, Yi Li, Johan M. Winne and Gerald Pattenden and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and The Journal of Organic Chemistry.

In The Last Decade

Christopher C. Nawrat

22 papers receiving 811 citations

Peers

Christopher C. Nawrat

PHARM

TOXIC

BIOTE

Yoshio Ando Japan

Enrique L. Larghi Argentina

Sabita Nayak India

Seetaram Mohapatra India

Alice Kanazawa France

Kei Kitamura Japan

M. HOSHINO Japan

Baochao Yang China

Gilles Dujardin France

Cristiano Raminelli Brazil

Yoshio Ando Japan

Christopher C. Nawrat

539 ×0.8

136 ×0.8

107 ×1.4

PHARM

110 ×1.5

TOXIC

77 ×1.2

BIOTE

Citations per year, relative to Christopher C. Nawrat Christopher C. Nawrat (= 1×) peers Yoshio Ando

Countries citing papers authored by Christopher C. Nawrat

Since Specialization

Citations

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

Fields of papers citing papers by Christopher C. Nawrat

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christopher C. Nawrat. 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 Christopher C. Nawrat. The network helps show where Christopher C. Nawrat may publish in the future.

Co-authorship network of co-authors of Christopher C. Nawrat

This figure shows the co-authorship network connecting the top 25 collaborators of Christopher C. Nawrat. A scholar is included among the top collaborators of Christopher C. Nawrat 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 Christopher C. Nawrat. Christopher C. Nawrat 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

Steven, Alan, Carlos Mateos, Christopher C. Nawrat, et al.. (2023). Some Items of Interest to Process R&D Chemists and Engineers. Organic Process Research & Development. 27(5). 811–821. 1 indexed citations

Steven, Alan, Robert B. Kargbo, Carlos Mateos, et al.. (2023). Some Items of Interest to Process R&D Chemists and Engineers. Organic Process Research & Development. 27(1). 1–9.

Richardson, Paul, Alan Steven, Robert B. Kargbo, et al.. (2022). Some Items of Interest to Process R&D Chemists and Engineers. Organic Process Research & Development. 26(1). 1–9. 2 indexed citations

Richardson, Paul, Alan Steven, Robert B. Kargbo, et al.. (2020). Some Items of Interest to Process R&D Chemists and Engineers. Organic Process Research & Development. 24(9). 1549–1557.

Ren, Sumei, Mark A. Huffman, Aaron M. Whittaker, et al.. (2020). Synthesis of Isotopically Labeled Anti-HIV Nucleoside Islatravir through a One-Pot Biocatalytic Cascade Reaction. Organic Process Research & Development. 25(3). 516–521. 7 indexed citations

Patel, Niki R., Christopher C. Nawrat, Mark McLaughlin, et al.. (2020). Synthesis of Islatravir Enabled by a Catalytic, Enantioselective Alkynylation of a Ketone. Organic Letters. 22(12). 4659–4664. 18 indexed citations

Nawrat, Christopher C., Aaron M. Whittaker, Mark A. Huffman, et al.. (2020). Nine-Step Stereoselective Synthesis of Islatravir from Deoxyribose. Organic Letters. 22(6). 2167–2172. 18 indexed citations

Richardson, Paul, Alan Steven, Robert B. Kargbo, et al.. (2018). Some Items of Interest to Process R&D Chemists and Engineers. Organic Process Research & Development. 22(3). 257–266.

Joyce, Leo A., Christopher C. Nawrat, Edward C. Sherer, et al.. (2017). Beyond optical rotation: what's left is not always right in total synthesis. Chemical Science. 9(2). 415–424. 23 indexed citations

10.

Richardson, Paul, Alan Steven, David P. Day, et al.. (2017). Some Items of Interest to Process R&D Chemists and Engineers. Organic Process Research & Development. 21(5). 675–688. 1 indexed citations

11.

Moody, Christopher J., et al.. (2015). Oxidative Routes to the Heterocyclic Cores of Benzothiazole Natural Products. Synlett. 27(1). 37–40. 11 indexed citations

12.

Nawrat, Christopher C. & Christopher J. Moody. (2014). Quinones as Dienophiles in the Diels–Alder Reaction: History and Applications in Total Synthesis. Angewandte Chemie International Edition. 53(8). 2056–2077. 124 indexed citations

13.

Lewis, William, et al.. (2014). Synthesis of toxyloxanthone B. Tetrahedron. 70(6). 1283–1288. 15 indexed citations

14.

Nawrat, Christopher C., Russell R. A. Kitson, & Christopher J. Moody. (2014). Toward the Total Synthesis of Hygrocin B and Divergolide C: Construction of the Naphthoquinone–Azepinone Core. Organic Letters. 16(7). 1896–1899. 21 indexed citations

15.

Nawrat, Christopher C., Leoni I. Palmer, Alexander J. Blake, & Christopher J. Moody. (2013). Two Approaches to the Aromatic Core of the Aminonaphthoquinone Antibiotics. The Journal of Organic Chemistry. 78(11). 5587–5603. 17 indexed citations

16.

Nawrat, Christopher C. & Christopher J. Moody. (2011). Natural products containing a diazo group. Natural Product Reports. 28(8). 1426–1426. 82 indexed citations

17.

Smith, Marcus J., Christopher C. Nawrat, & Christopher J. Moody. (2011). Synthesis of Parvistemin A via Biomimetic Oxidative Dimerization. Organic Letters. 13(13). 3396–3398. 13 indexed citations

18.

Nawrat, Christopher C., William Lewis, & Christopher J. Moody. (2011). Synthesis of Amino-1,4-benzoquinones and Their Use in Diels–Alder Approaches to the Aminonaphthoquinone Antibiotics. The Journal of Organic Chemistry. 76(19). 7872–7881. 25 indexed citations

19.

Li, Yi, Christopher C. Nawrat, Gerald Pattenden, & Johan M. Winne. (2009). Synthesis of ()-Anthecularin. Synfacts. 2009(8). 822–822. 1 indexed citations

20.

Li, Yi, Christopher C. Nawrat, Gerald Pattenden, & Johan M. Winne. (2008). A concise total synthesis of (±)-anthecularin. Organic & Biomolecular Chemistry. 7(4). 639–640. 20 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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