James H. Babler

975 total citations
55 papers, 659 citations indexed

About

James H. Babler is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, James H. Babler has authored 55 papers receiving a total of 659 indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Organic Chemistry, 14 papers in Molecular Biology and 8 papers in Inorganic Chemistry. Recurrent topics in James H. Babler's work include Asymmetric Synthesis and Catalysis (16 papers), Chemical Synthesis and Reactions (14 papers) and Chemical Synthesis and Analysis (11 papers). James H. Babler is often cited by papers focused on Asymmetric Synthesis and Catalysis (16 papers), Chemical Synthesis and Reactions (14 papers) and Chemical Synthesis and Analysis (11 papers). James H. Babler collaborates with scholars based in United States. James H. Babler's co-authors include Michael J. Coghlan, Benedict J. Invergo, Kenneth P. Spina, Douglas O. Olsen, Michael J. Martin, James J. Kiddle, William Buttner, Richard A. Haack, James A. Marshall and William E. Bauta and has published in prestigious journals such as The Journal of Organic Chemistry, Tetrahedron Letters and Synthetic Communications.

In The Last Decade

James H. Babler

53 papers receiving 616 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
James H. Babler United States 15 548 192 97 38 37 55 659
Leland O. Weigel United States 14 421 0.8× 183 1.0× 66 0.7× 26 0.7× 27 0.7× 25 577
R. BERNARDI Italy 12 689 1.3× 149 0.8× 67 0.7× 23 0.6× 94 2.5× 30 824
M. Rambaud France 15 518 0.9× 161 0.8× 67 0.7× 19 0.5× 44 1.2× 20 580
V. K. AHUJA India 4 318 0.6× 91 0.5× 93 1.0× 48 1.3× 34 0.9× 6 503
Conrad J. Kowalski United Kingdom 17 675 1.2× 165 0.9× 98 1.0× 17 0.4× 53 1.4× 24 784
Martha A. Umbreit 4 452 0.8× 230 1.2× 52 0.5× 42 1.1× 22 0.6× 6 642
G. LHOMMET France 23 1.4k 2.6× 312 1.6× 101 1.0× 27 0.7× 51 1.4× 102 1.5k
Mihailo Lj. Mihailovíć Serbia 11 444 0.8× 240 1.3× 69 0.7× 32 0.8× 27 0.7× 45 608
Michael J. Umen United States 7 397 0.7× 86 0.4× 65 0.7× 24 0.6× 31 0.8× 9 463
K. Eiter Germany 14 469 0.9× 166 0.9× 57 0.6× 32 0.8× 36 1.0× 34 613

Countries citing papers authored by James H. Babler

Since Specialization
Citations

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

Fields of papers citing papers by James H. Babler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by James H. Babler. 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 James H. Babler. The network helps show where James H. Babler may publish in the future.

Co-authorship network of co-authors of James H. Babler

This figure shows the co-authorship network connecting the top 25 collaborators of James H. Babler. A scholar is included among the top collaborators of James H. Babler 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 James H. Babler. James H. Babler 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
2.
Babler, James H., et al.. (1996). Alkoxide-Catalyzed Addition of Terminal Alkynes to Ketones. The Journal of Organic Chemistry. 61(1). 416–417. 37 indexed citations
3.
Babler, James H., Charles J. Marcuccilli, & John E. Oblong. (1990). Base Promoted Rearrangement of Carbonate Esters Derived from Aldehyde Cyanohydrins: Application to the Synthesis of α-Keto Esters. Synthetic Communications. 20(12). 1831–1836. 7 indexed citations
4.
Babler, James H. & Kenneth P. Spina. (1984). ChemInform Abstract: A FACILE AND EFFICIENT METHOD FOR MONOKETALIZATION OF 1,4‐CYCLOHEXANEDIONE. Chemischer Informationsdienst. 15(45). 2 indexed citations
5.
Babler, James H. & Kenneth P. Spina. (1984). A Facile Method for the Conversion of Primary Alkyl Chlorides to the Corresponding Bromides. Synthetic Communications. 14(14). 1313–1319. 7 indexed citations
7.
Babler, James H., et al.. (1982). ChemInform Abstract: NON‐CATALYZED REDUCTIONS WITH FORMATE SALTS: CONVERSION OF NITROAROMATIC COMPOUNDS TO THE CORRESPONDING PRIMARY AMINES. Chemischer Informationsdienst. 13(32). 1 indexed citations
8.
Babler, James H. & Benedict J. Invergo. (1981). A facile route to a versatile synthon for preparation of -pyrethroids. Tetrahedron Letters. 22(29). 2743–2746. 2 indexed citations
9.
Babler, James H. & Benedict J. Invergo. (1981). A facile biomimetic method for oxidative deamination of primary amines to aldehydes via transposition of an imine functionality. The Journal of Organic Chemistry. 46(9). 1937–1938. 15 indexed citations
10.
Babler, James H. & Benedict J. Invergo. (1980). ChemInform Abstract: A CONVENIENT STEREOSELECTIVE ROUTE TO THE SEX PHEROMONE OF THE RED BOLLWORM MOTH VIA AN ALLYLIC SULFENATE TO SULFOXIDE REARRANGEMENT. Chemischer Informationsdienst. 11(7). 5 indexed citations
11.
Babler, James H., et al.. (1979). イソプレンクロロヒドリンから4‐アセトキシ‐2‐メチル‐2‐ブテナール,ビタミンA先駆体の容易な合成. The Journal of Organic Chemistry. 44(10). 1716–1717. 11 indexed citations
12.
Babler, James H. & Benedict J. Invergo. (1979). A convenient stereoselective route to the sex pheromone of the red bollworm moth via an allylic sulfenate to sulfoxide rearrangement. The Journal of Organic Chemistry. 44(21). 3723–3724. 16 indexed citations
13.
Babler, James H. & Michael J. Coghlan. (1979). A facile method for monoacetylation of symmetrical diols: application to the total synthesis of Z-8-dodecenyl acetate, the sex attractant of the oriental fruit moth. Tetrahedron Letters. 20(22). 1971–1974. 38 indexed citations
14.
Babler, James H. & Michael J. Martin. (1977). A facile synthesis of the sex pheromone of the red bollworm moth from 10-undecen-1-ol. The Journal of Organic Chemistry. 42(10). 1799–1800. 17 indexed citations
16.
Babler, James H. & William Buttner. (1976). A facile route to E-4-bromo-3-methyl-2-buten-1-ol: Application to the stereoselective synthesis of trisubstituted olefins. Tetrahedron Letters. 17(4). 239–242. 20 indexed citations
17.
Babler, James H.. (1975). Base-promoted cyclization of a δ-chloro ester: Application to the total stynthesis of (±)-grandisol. Tetrahedron Letters. 16(25). 2045–2048. 8 indexed citations
18.
Babler, James H. & Douglas O. Olsen. (1974). A facile method for the bishomologation of ketones to functionalized trisubstituted olefins. Tetrahedron Letters. 15(4). 351–354. 19 indexed citations
19.
Babler, James H., Douglas O. Olsen, & William H. Arnold. (1974). Total stereoselective synthesis of .alpha.-atlantone. The Journal of Organic Chemistry. 39(12). 1656–1658. 16 indexed citations
20.
Marshall, James A. & James H. Babler. (1969). Heterolytic fragmentation of 1-substituted decahydroquinolines. The Journal of Organic Chemistry. 34(12). 4186–4188. 9 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026