Jillian E. Spangler

3.2k total citations · 3 hit papers
16 papers, 2.4k citations indexed

About

Jillian E. Spangler is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, Jillian E. Spangler has authored 16 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Organic Chemistry, 5 papers in Inorganic Chemistry and 1 paper in Molecular Biology. Recurrent topics in Jillian E. Spangler's work include Catalytic C–H Functionalization Methods (11 papers), Synthesis and Catalytic Reactions (6 papers) and Cyclopropane Reaction Mechanisms (6 papers). Jillian E. Spangler is often cited by papers focused on Catalytic C–H Functionalization Methods (11 papers), Synthesis and Catalytic Reactions (6 papers) and Cyclopropane Reaction Mechanisms (6 papers). Jillian E. Spangler collaborates with scholars based in United States, China and France. Jillian E. Spangler's co-authors include Huw M. L. Davies, Jin‐Quan Yu, Suhua Li, Brian N. Laforteza, Jian He, Youqian Deng, Haiyan Fu, Anna Homs, Gary M. Gallego and Michael R. Collins and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Jillian E. Spangler

16 papers receiving 2.4k citations

Hit Papers

Ligand-Controlled C(sp 3 )–H Arylation and Olefination in... 2014 2026 2018 2022 2014 2016 2019 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jillian E. Spangler United States 14 2.3k 331 228 194 67 16 2.4k
Giulia Bergonzini Sweden 18 2.1k 0.9× 363 1.1× 179 0.8× 254 1.3× 131 2.0× 21 2.2k
Ryan Gianatassio United States 12 2.3k 1.0× 275 0.8× 245 1.1× 415 2.1× 35 0.5× 13 2.5k
Jay C. Conrad United States 19 1.4k 0.6× 249 0.8× 381 1.7× 185 1.0× 51 0.8× 32 1.5k
Chandra M. R. Volla India 33 3.6k 1.6× 507 1.5× 258 1.1× 155 0.8× 31 0.5× 94 3.7k
Alexander P. Pulis United Kingdom 27 2.2k 1.0× 384 1.2× 180 0.8× 162 0.8× 45 0.7× 44 2.3k
Zhenhua Zhang China 21 2.0k 0.9× 335 1.0× 157 0.7× 170 0.9× 38 0.6× 45 2.2k
Malcolm Spain United Kingdom 23 1.3k 0.6× 426 1.3× 252 1.1× 216 1.1× 100 1.5× 29 1.6k
Mattia Silvi United Kingdom 20 2.0k 0.9× 182 0.5× 146 0.6× 235 1.2× 118 1.8× 26 2.1k
Eddie L. Myers United Kingdom 26 2.6k 1.2× 382 1.2× 357 1.6× 195 1.0× 51 0.8× 39 2.8k
James J. Mousseau United States 28 3.3k 1.5× 504 1.5× 371 1.6× 401 2.1× 71 1.1× 46 3.6k

Countries citing papers authored by Jillian E. Spangler

Since Specialization
Citations

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

Fields of papers citing papers by Jillian E. Spangler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jillian E. Spangler. 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 Jillian E. Spangler. The network helps show where Jillian E. Spangler may publish in the future.

Co-authorship network of co-authors of Jillian E. Spangler

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

All Works

16 of 16 papers shown
1.
Li, Jian, Indrawan McAlpine, Sajiv K. Nair, et al.. (2025). Microwave-Assisted Synthesis of Heterocycles via Rhodium(III)-Catalyzed C–H Activation: Norbornadiene as an Acetylene Equivalent. Organic Letters. 27(3). 728–733. 1 indexed citations
2.
Zhao, Jin‐Xin, Chi He, Benjamin J. Burke, et al.. (2021). 1,2-Difunctionalized bicyclo[1.1.1]pentanes: Long–sought-after mimetics for ortho / meta -substituted arenes. Proceedings of the National Academy of Sciences. 118(28). 101 indexed citations
3.
Barber, Joyann S., Michael R. Collins, Michelle Tran‐Dubé, et al.. (2020). Development of a Late-Stage Diversification Strategy for the 4- and 5-Positions of 4,5,6-Trisubstituted Indazoles. Organic Letters. 22(22). 9047–9052. 2 indexed citations
4.
Xiang, Jinbao, Ming Shang, Yu Kawamata, et al.. (2019). Hindered dialkyl ether synthesis with electrogenerated carbocations. Nature. 573(7774). 398–402. 311 indexed citations breakdown →
5.
Gianatassio, Ryan, Justin M. Lopchuk, Jie Wang, et al.. (2016). Strain-release amination. Science. 351(6270). 241–246. 452 indexed citations breakdown →
6.
Spangler, Jillian E., Yoshihisa Kobayashi, Pritha Verma, Dong‐Hui Wang, & Jin‐Quan Yu. (2015). α-Arylation of Saturated Azacycles and N-Methylamines via Palladium(II)-Catalyzed C(sp3)–H Coupling. Journal of the American Chemical Society. 137(37). 11876–11879. 154 indexed citations
7.
Lu, Yi, Huaiwei Wang, Jillian E. Spangler, et al.. (2015). Rh(iii)-catalyzed C–H olefination of N-pentafluoroaryl benzamides using air as the sole oxidant. Chemical Science. 6(3). 1923–1927. 106 indexed citations
8.
Li, Gang, Li Wan, Guofu Zhang, et al.. (2015). Pd(II)-Catalyzed C–H Functionalizations Directed by Distal Weakly Coordinating Functional Groups. Journal of the American Chemical Society. 137(13). 4391–4397. 151 indexed citations
9.
He, Jian, Suhua Li, Youqian Deng, et al.. (2014). Ligand-Controlled C(sp 3 )–H Arylation and Olefination in Synthesis of Unnatural Chiral α–Amino Acids. Science. 343(6176). 1216–1220. 468 indexed citations breakdown →
10.
Spangler, Jillian E., et al.. (2014). Synthesis of Complex Hexacyclic Compounds via a Tandem Rh(II)-Catalyzed Double-Cyclopropanation/Cope Rearrangement/Diels–Alder Reaction. Organic Letters. 16(18). 4794–4797. 17 indexed citations
11.
He, Jian, Suhua Li, Youqian Deng, et al.. (2014). ChemInform Abstract: Ligand‐Controlled C(sp3)‐H Arylation and Olefination in Synthesis of Unnatural Chiral α‐Amino Acids.. ChemInform. 45(39). 38 indexed citations
12.
Alford, Joshua S., Jillian E. Spangler, & Huw M. L. Davies. (2013). Conversion of Cyclic Ketones to 2,3-Fused Pyrroles and Substituted Indoles. Journal of the American Chemical Society. 135(32). 11712–11715. 155 indexed citations
13.
Spangler, Jillian E. & Huw M. L. Davies. (2013). Catalytic Asymmetric Synthesis of Pyrroloindolines via a Rhodium(II)-Catalyzed Annulation of Indoles. Journal of the American Chemical Society. 135(18). 6802–6805. 340 indexed citations
14.
Spangler, Jillian E., et al.. (2012). Metal-Free N–H Insertions of Donor/Acceptor Carbenes. Organic Letters. 14(17). 4626–4629. 74 indexed citations
15.
Spangler, Jillian E., Cheryl A. Carson, & Erik J. Sorensen. (2010). Synthesis enables a structural revision of the Mycobacterium tuberculosis-produced diterpene, edaxadiene. Chemical Science. 1(2). 202–202. 18 indexed citations
16.
Spangler, Jillian E. & Erik J. Sorensen. (2009). A nature-inspired Diels–Alder reaction facilitates construction of the bicyclo[2.2.2]octane core of andibenin B. Tetrahedron. 65(33). 6739–6745. 16 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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