Rich G. Carter

3.6k total citations
96 papers, 3.0k citations indexed

About

Rich G. Carter is a scholar working on Organic Chemistry, Biotechnology and Environmental Chemistry. According to data from OpenAlex, Rich G. Carter has authored 96 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 76 papers in Organic Chemistry, 18 papers in Biotechnology and 14 papers in Environmental Chemistry. Recurrent topics in Rich G. Carter's work include Synthetic Organic Chemistry Methods (42 papers), Asymmetric Synthesis and Catalysis (34 papers) and Chemical synthesis and alkaloids (27 papers). Rich G. Carter is often cited by papers focused on Synthetic Organic Chemistry Methods (42 papers), Asymmetric Synthesis and Catalysis (34 papers) and Chemical synthesis and alkaloids (27 papers). Rich G. Carter collaborates with scholars based in United States, Japan and Egypt. Rich G. Carter's co-authors include Hua Yang, B.O. Ashburn, Lev N. Zakharov, Subham Mahapatra, Xiulei Ji, Xiao‐Ti Zhou, James D. White, Paul Ha‐Yeon Cheong, Kurt F. Sundermann and Clement Bommier and has published in prestigious journals such as Science, Journal of the American Chemical Society and Angewandte Chemie International Edition.

In The Last Decade

Rich G. Carter

95 papers receiving 2.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rich G. Carter United States 32 2.1k 562 422 290 276 96 3.0k
Arnab Chatterjee United States 22 3.4k 1.6× 345 0.6× 1.4k 3.4× 363 1.3× 186 0.7× 54 3.8k
Jin Kun United States 40 4.4k 2.0× 153 0.3× 769 1.8× 296 1.0× 114 0.4× 181 5.4k
Bernd Schmidt Germany 35 3.3k 1.5× 99 0.2× 1.0k 2.4× 213 0.7× 122 0.4× 157 3.7k
Joëlle Prunet France 23 1.7k 0.8× 54 0.1× 579 1.4× 307 1.1× 101 0.4× 78 1.9k
Steven T. Diver United States 28 3.5k 1.6× 134 0.2× 1.3k 3.1× 144 0.5× 106 0.4× 75 3.9k
Matthias Scholl United States 9 4.8k 2.2× 386 0.7× 1.8k 4.4× 502 1.7× 319 1.2× 11 5.0k
Sung Ho Kang South Korea 26 1.0k 0.5× 267 0.5× 294 0.7× 129 0.4× 57 0.2× 76 2.2k
Marcia B. France United States 15 1.9k 0.9× 182 0.3× 835 2.0× 122 0.4× 94 0.3× 20 2.1k
Karol Grela Poland 50 8.2k 3.8× 1.1k 1.9× 3.4k 8.2× 257 0.9× 219 0.8× 236 8.7k
Ferdinando Pizzo Italy 40 3.5k 1.6× 75 0.1× 812 1.9× 46 0.2× 237 0.9× 115 3.9k

Countries citing papers authored by Rich G. Carter

Since Specialization
Citations

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

Fields of papers citing papers by Rich G. Carter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rich G. Carter. 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 Rich G. Carter. The network helps show where Rich G. Carter may publish in the future.

Co-authorship network of co-authors of Rich G. Carter

This figure shows the co-authorship network connecting the top 25 collaborators of Rich G. Carter. A scholar is included among the top collaborators of Rich G. Carter 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 Rich G. Carter. Rich G. Carter 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.
Bouwma‐Gearhart, Jana, et al.. (2020). STEM Graduate Students’ Development at the Intersection of Research, Leadership, and Innovation. SSRN Electronic Journal. 2 indexed citations
2.
Harada, Kenichi, et al.. (2019). Asymmetric Construction of Vicinal Stereocenters Containing Quaternary and Tertiary Carbons: Application to the Formal Synthesis of (–)‐Chenopodene. European Journal of Organic Chemistry. 2020(4). 420–423. 4 indexed citations
3.
Carter, Rich G., et al.. (2018). Recent Syntheses and Strategies toward Polycyclic Gelsemium Alkaloids. Angewandte Chemie International Edition. 58(3). 681–694. 23 indexed citations
4.
Yang, Hua, et al.. (2012). Proline sulphonamide-catalysed Yamada–Otani condensation: reaction development, substrate scope and scaffold reactivity. Organic & Biomolecular Chemistry. 10(25). 4851–4851. 18 indexed citations
5.
Johnston, Ryne C., et al.. (2012). Mechanism and Stereoselectivity of a Dual Amino-Catalyzed Robinson Annulation: Rare Duumvirate Stereocontrol. Journal of the American Chemical Society. 134(33). 13624–13631. 33 indexed citations
6.
Kang, Jun Yong & Rich G. Carter. (2012). Primary Amine, Thiourea-Based Dual Catalysis Motif for Synthesis of Stereogenic, All-Carbon Quaternary Center-Containing Cycloalkanones. Organic Letters. 14(12). 3178–3181. 48 indexed citations
7.
Mahapatra, Subham & Rich G. Carter. (2012). Enantioselective Total Synthesis of Amphidinolide F. Angewandte Chemie International Edition. 51(32). 7948–7951. 42 indexed citations
8.
Carter, Rich G., et al.. (2011). Stereoselective Synthesis of the Eastern Quinolizidine Portion of Himeradine A. Organic Letters. 13(15). 4144–4147. 18 indexed citations
9.
Yang, Hua & Rich G. Carter. (2010). Organocatalyzed, enantioselective synthesis of bicyclo-[2.2.2]-octanes containing benzylic, all-carbon quaternary centers. Tetrahedron. 66(26). 4854–4859. 20 indexed citations
10.
Carter, Rich G., et al.. (2010). Moving backwards in new ways. Nature Chemistry. 2(8). 613–614. 2 indexed citations
11.
Mahapatra, Subham & Rich G. Carter. (2009). Efficient synthesis of the C7-C20 subunit of amphidinolides C and F. Organic & Biomolecular Chemistry. 7(22). 4582–4582. 26 indexed citations
12.
Ashburn, B.O. & Rich G. Carter. (2008). Diels–Alder approach to biaryls (DAB): Importance of the ortho-nitro moiety in the [4 + 2] cycloaddition. Organic & Biomolecular Chemistry. 6(2). 255–257. 13 indexed citations
13.
Zhou, Xiao‐Ti, et al.. (2006). Synthesis of the Southern FGHI Ring System of Azaspiracid‐1 and Investigation into the Controlling Elements of C28‐ and C36‐Ketalization. Angewandte Chemie International Edition. 45(45). 7622–7626. 30 indexed citations
14.
Ashburn, B.O. & Rich G. Carter. (2006). Diels–Alder Approach to Polysubstituted Biaryls: Rapid Entry to Tri‐ and Tetra‐ortho‐substituted Phosphorus‐Containing Biaryls. Angewandte Chemie International Edition. 45(40). 6737–6741. 61 indexed citations
15.
Zhou, Xiao‐Ti & Rich G. Carter. (2006). Synthesis of the C1–C26 Northern Portion of Azaspiracid‐1: Kinetic versus Thermodynamic Control of the Formation of the Bis‐spiroketal. Angewandte Chemie. 118(11). 1819–1822. 15 indexed citations
16.
Ashburn, B.O. & Rich G. Carter. (2006). Diels–Alder Approach to Polysubstituted Biaryls: Rapid Entry to Tri‐ and Tetra‐ortho‐substituted Phosphorus‐Containing Biaryls. Angewandte Chemie. 118(40). 6889–6893. 10 indexed citations
17.
Zhou, Xiao‐Ti & Rich G. Carter. (2006). Synthesis of the C1–C26 Northern Portion of Azaspiracid‐1: Kinetic versus Thermodynamic Control of the Formation of the Bis‐spiroketal. Angewandte Chemie International Edition. 45(11). 1787–1790. 37 indexed citations
18.
Zhou, Xiao‐Ti & Rich G. Carter. (2004). Synthesis of the ABCD and ABCDE ring systems of azaspiracid-1. Chemical Communications. 2138–2138. 27 indexed citations
19.
White, James D., Rich G. Carter, Kurt F. Sundermann, & Markus Wartmann. (2003). Total Synthesis of Epothilone B, Epothilone D, and cis- and trans-9,10-Dehydroepothilone D  [J. Am. Chem. Soc. 2001, 123, 5407−5413].. Journal of the American Chemical Society. 125(10). 3190–3190. 9 indexed citations
20.
White, James D., Rich G. Carter, & Kurt F. Sundermann. (1999). A Highly Stereoselective Synthesis of Epothilone B. The Journal of Organic Chemistry. 64(3). 684–685. 56 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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