Ulf‐H. Dolling

2.2k total citations · 1 hit paper
48 papers, 1.7k citations indexed

About

Ulf‐H. Dolling is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, Ulf‐H. Dolling has authored 48 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Organic Chemistry, 16 papers in Molecular Biology and 8 papers in Inorganic Chemistry. Recurrent topics in Ulf‐H. Dolling's work include Asymmetric Synthesis and Catalysis (13 papers), Chemical Synthesis and Analysis (13 papers) and Synthetic Organic Chemistry Methods (9 papers). Ulf‐H. Dolling is often cited by papers focused on Asymmetric Synthesis and Catalysis (13 papers), Chemical Synthesis and Analysis (13 papers) and Synthetic Organic Chemistry Methods (9 papers). Ulf‐H. Dolling collaborates with scholars based in United States, United Kingdom and Japan. Ulf‐H. Dolling's co-authors include Daniel R. Sidler, Essa Hu, Edward J. J. Grabowski, David M. Tschaen, J. Michael Williams, Sandor Karady, Ian F. Cottrell, Nobuyoshi Yasuda, Antony J. Davies and Cameron J. Cowden and has published in prestigious journals such as Journal of the American Chemical Society, Annals of the New York Academy of Sciences and The Journal of Organic Chemistry.

In The Last Decade

Ulf‐H. Dolling

46 papers receiving 1.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Unprecedented Catalytic Three Component One-Pot Condensation Reaction: An Efficient Synthesis of 5-Alkoxycarbonyl- 4-aryl-3,4-dihydropyrimidin-2(1H)-ones

1998 450 citations Daniel R. Sidler, Ulf‐H. Dolling et al. The Journal of Organic Chemistry profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ulf‐H. Dolling United States	23	1.5k	475	276	168	91	48	1.7k
Yuusaku Yokoyama Japan	24	1.8k 1.2×	640 1.3×	308 1.1×	121 0.7×	89 1.0×	105	2.1k
James M. McNamara United States	20	968 0.7×	444 0.9×	152 0.6×	108 0.6×	116 1.3×	42	1.3k
Edward G. Corley United States	20	1.4k 1.0×	423 0.9×	312 1.1×	86 0.5×	106 1.2×	39	1.6k
Chad A. Lewis United States	18	1.1k 0.8×	582 1.2×	229 0.8×	204 1.2×	69 0.8×	32	1.4k
Maria D. Rozwadowska Poland	17	1.6k 1.1×	311 0.7×	280 1.0×	156 0.9×	87 1.0×	65	1.8k
Sepehr Sarshar United States	21	1.1k 0.8×	656 1.4×	273 1.0×	74 0.4×	144 1.6×	28	1.6k
Tadakatsu Mandai Japan	27	2.1k 1.4×	481 1.0×	339 1.2×	125 0.7×	97 1.1×	113	2.4k
Simonetta Benetti Italy	23	1.8k 1.2×	589 1.2×	183 0.7×	150 0.9×	118 1.3×	106	2.0k
Todd D. Nelson United States	20	1.2k 0.8×	308 0.6×	177 0.6×	93 0.6×	163 1.8×	42	1.4k
Gema Domı́nguez Spain	25	2.4k 1.7×	529 1.1×	353 1.3×	113 0.7×	83 0.9×	97	2.7k

Countries citing papers authored by Ulf‐H. Dolling

Since Specialization

Citations

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

Fields of papers citing papers by Ulf‐H. Dolling

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ulf‐H. Dolling. 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 Ulf‐H. Dolling. The network helps show where Ulf‐H. Dolling may publish in the future.

Co-authorship network of co-authors of Ulf‐H. Dolling

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Scott, Jeremy P., David Lieberman, Karel M. J. Brands, et al.. (2007). A Practical Synthesis of a γ-Secretase Inhibitor. The Journal of Organic Chemistry. 72(11). 4149–4155. 30 indexed citations

Scott, Jeremy P., Michael S. Ashwood, Karel M. J. Brands, et al.. (2007). Development of a Phase Transfer Catalyzed Asymmetric Synthesis for an Estrogen Receptor Beta Selective Agonist. Organic Process Research & Development. 12(4). 723–730. 26 indexed citations

Scott, Jeremy P., Sarah E. Brewer, Karel M. J. Brands, et al.. (2006). The conformational bias of aryl, arylsulfonyl geminally substituted tertiary carbon centers: applications in substrate-based stereocontrol. Organic & Biomolecular Chemistry. 4(9). 1806–1806. 1 indexed citations

Cameron, Mark, Bruce S. Foster, Joseph E. Lynch, Yao‐Jun Shi, & Ulf‐H. Dolling. (2006). The Expedient Synthesis of 4,2‘-Difluoro-5‘-(7-trifluoromethyl- imidazo[1,2-a]pyrimidin-3-yl)biphenyl-2-carbonitrile, a GABA α2/3 Agonist. Organic Process Research & Development. 10(3). 398–402. 33 indexed citations

Engelhardt, Felix, Yao‐Jun Shi, Cameron J. Cowden, et al.. (2005). Synthesis of a NO-Releasing Prodrug of Rofecoxib. The Journal of Organic Chemistry. 71(2). 480–491. 24 indexed citations

Williams, J. Michael, Karel M. J. Brands, Renato T. Skerlj, et al.. (2005). Practical Synthesis of the New Carbapenem Antibiotic Ertapenem Sodium. The Journal of Organic Chemistry. 70(19). 7479–7487. 15 indexed citations

Scott, Jeremy P., Elizabeth M. Beck, Karel M. J. Brands, et al.. (2004). Expedient Diels–Alder assembly of 4-aryl-4-phenylsulfonyl cyclohexanones. Tetrahedron Letters. 45(17). 3345–3348. 12 indexed citations

Zhao, Matthew M., James M. McNamara, Khateeta M. Emerson, et al.. (2002). Practical Asymmetric Synthesis of Aprepitant, a Potent Human NK-1 Receptor Antagonist, via a Stereoselective Lewis Acid-Catalyzed Trans Acetalization Reaction. The Journal of Organic Chemistry. 67(19). 6743–6747. 54 indexed citations

Brands, Karel M. J., Ronald B. Jobson, Karen M. Conrad, et al.. (2002). Efficient One-Pot Synthesis of the 2-Aminocarbonylpyrrolidin-4-ylthio-Containing Side Chain of the New Broad-Spectrum Carbapenem Antibiotic Ertapenem. The Journal of Organic Chemistry. 67(14). 4771–4776. 18 indexed citations

10.

Wallace, Debra J., Jonathan M. Goodman, Derek J. Kennedy, et al.. (2001). A Double Ring Closing Metathesis Reaction in the Rapid, Enantioselective Synthesis of NK-1 Receptor Antagonists. Organic Letters. 3(5). 671–674. 51 indexed citations

11.

Cowden, Cameron J., Robert D. Wilson, Brian Bishop, et al.. (2001). ChemInform Abstract: A New Synthesis of 1,2,4‐Triazolin‐5‐ones: Application to the Convergent Synthesis of an NK₁ Antagonist.. ChemInform. 32(4). 1 indexed citations

12.

Cowden, Cameron J., Robert D. Wilson, Brian Bishop, et al.. (2000). A new synthesis of 1,2,4-triazolin-5-ones: application to the convergent synthesis of an NK1 antagonist. Tetrahedron Letters. 41(44). 8661–8664. 28 indexed citations

13.

Wallace, Debra J., Cameron J. Cowden, Derek J. Kennedy, et al.. (2000). ChemInform Abstract: Stereoselective Double Ring Closing Metathesis Reactions in the Synthesis of Spirocyclic Compounds.. ChemInform. 31(25).

14.

Wallace, Debra J., Cameron J. Cowden, Derek J. Kennedy, et al.. (2000). Stereoselective double ring closing metathesis reactions in the synthesis of spirocyclic compounds. Tetrahedron Letters. 41(12). 2027–2029. 40 indexed citations

15.

Yasuda, Nobuyoshi, Mark A. Huffman, Lyndon C. Xavier, et al.. (1998). Practical Synthesis of Anti-Methicillin-Resistant Staphylococcus Aureus (MRSA) Carbapenem L-742,728. The Journal of Organic Chemistry. 63(16). 5438–5446. 24 indexed citations

16.

Williams, J. Michael, et al.. (1995). A new general method for preparation of N-methoxy-N-methylamides. Application in direct conversion of an ester to a ketone. Tetrahedron Letters. 36(31). 5461–5464. 168 indexed citations

17.

Carlin, Josephine R., et al.. (1994). Biotransformation of Finasteride (MK‐0906) bySelenastrum capricornutum(Green Algae). Annals of the New York Academy of Sciences. 745(1). 51–60. 2 indexed citations

18.

Yasuda, Nobuyoshi, Lyndon C. Xavier, Dale L. Rieger, et al.. (1993). Preparation of 2-aryl- and 2-alkenyl-substituted carbapenems under mild suzuki cross-coupling conditions. Tetrahedron Letters. 34(20). 3211–3214. 28 indexed citations

19.

Hughes, Dave, Ulf‐H. Dolling, K. M. RYAN, Erwin F. Schoenewaldt, & Edward J. J. Grabowski. (1987). Efficient catalytic asymmetric alkylations. 3. A kinetic and mechanistic study of the enantioselective phase-transfer methylation of 6,7-dichloro-5-methoxy-2-phenyl-1-indanone. The Journal of Organic Chemistry. 52(21). 4745–4752. 124 indexed citations

20.

Dolling, Ulf‐H., et al.. (1967). A Topological Approach to the Problem of Ring Structures. Angewandte Chemie International Edition in English. 6(9). 723–733. 11 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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