Thomas E. Cole

1.3k total citations
31 papers, 886 citations indexed

About

Thomas E. Cole is a scholar working on Organic Chemistry, Inorganic Chemistry and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Thomas E. Cole has authored 31 papers receiving a total of 886 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Organic Chemistry, 13 papers in Inorganic Chemistry and 6 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Thomas E. Cole's work include Organoboron and organosilicon chemistry (14 papers), Asymmetric Hydrogenation and Catalysis (12 papers) and Chemical Synthesis and Reactions (10 papers). Thomas E. Cole is often cited by papers focused on Organoboron and organosilicon chemistry (14 papers), Asymmetric Hydrogenation and Catalysis (12 papers) and Chemical Synthesis and Reactions (10 papers). Thomas E. Cole collaborates with scholars based in United States and Mexico. Thomas E. Cole's co-authors include Herbert C. Brown, Morris Srebnik, Bakthan Singaram, R. Pettit, R. Ramage, Kevin Cann, Ratnasamy Somanathan, Stephan Rodewald, Miguel Parra‐Hake and Gerardo Aguirre and has published in prestigious journals such as Journal of the American Chemical Society, The Journal of Organic Chemistry and Tetrahedron.

In The Last Decade

Thomas E. Cole

30 papers receiving 846 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas E. Cole United States 16 752 271 123 69 58 31 886
Ralph B. Nielsen United States 11 829 1.1× 290 1.1× 59 0.5× 60 0.9× 24 0.4× 12 906
Charles E. Tucker Germany 17 1.2k 1.6× 211 0.8× 170 1.4× 56 0.8× 31 0.5× 24 1.3k
Jin Soon South Korea 17 600 0.8× 354 1.3× 274 2.2× 113 1.6× 11 0.2× 81 818
James E. Galle United States 19 1.1k 1.4× 306 1.1× 94 0.8× 128 1.9× 30 0.5× 28 1.1k
Bernard Garrigues France 19 851 1.1× 180 0.7× 167 1.4× 78 1.1× 9 0.2× 94 968
Urs Burckhardt Switzerland 19 1.1k 1.5× 703 2.6× 205 1.7× 45 0.7× 14 0.2× 27 1.3k
Teresa Mancilla Mexico 16 710 0.9× 321 1.2× 157 1.3× 100 1.4× 55 0.9× 61 874
Kevin R. Flower United Kingdom 18 676 0.9× 365 1.3× 75 0.6× 95 1.4× 20 0.3× 72 917
Charles F. Nutaitis United States 10 377 0.5× 133 0.5× 163 1.3× 53 0.8× 11 0.2× 25 489
Gilbert Meyer France 21 1.2k 1.6× 334 1.2× 202 1.6× 73 1.1× 22 0.4× 33 1.3k

Countries citing papers authored by Thomas E. Cole

Since Specialization
Citations

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

Fields of papers citing papers by Thomas E. Cole

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas E. Cole

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas E. Cole. A scholar is included among the top collaborators of Thomas E. Cole 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 Thomas E. Cole. Thomas E. Cole 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.
Cortez‐Lemus, Norma A., et al.. (2006). New C2-symmetric bis(sulfonamide)-cyclohexane-1,2-diamine-RhCp∗ complex and its application in the asymmetric transfer hydrogenation (ATH) of ketones in water. Tetrahedron Letters. 47(48). 8515–8518. 36 indexed citations
2.
Cole, Thomas E., et al.. (1997). Transmetalation of organic groups from zirconacycles to haloboranes: A new route to borolane compounds. Tetrahedron Letters. 38(49). 8487–8490. 9 indexed citations
3.
Cole, Thomas E., et al.. (1992). Simple conversion of anhydrides of boronic and borinic acids to the corresponding organodihaloboranes and diorganohaloboranes. Tetrahedron Letters. 33(20). 2761–2764. 8 indexed citations
4.
Cole, Thomas E., et al.. (1992). Transmetalation of disubstituted alkenyl groups from zirconium to boron compounds. The Journal of Organic Chemistry. 57(26). 7366–7370. 16 indexed citations
5.
Cole, Thomas E., et al.. (1992). Selective preparation of borinic esters from Grignard reagents and selected trialkoxyboranes. Organometallics. 11(2). 652–657. 16 indexed citations
6.
Cole, Thomas E., et al.. (1990). A Simple and Convenient Method for Synthesizing Trialkoxyboranes and Trialkoxyboroxins Using Calcium Hydride as a Drying Agent. Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry. 20(1). 55–63. 9 indexed citations
9.
Srebnik, Morris, Thomas E. Cole, & Herbert C. Brown. (1987). Methylborane - a remarkable unhindered monoalkylborane which achieves the controlled sequential hydroboration of representative alkenes. Tetrahedron Letters. 28(33). 3771–3774. 2 indexed citations
10.
Cole, Thomas E., Raman K. Bakshi, Morris Srebnik, Bakthan Singaram, & Herbert C. Brown. (1986). Organoboranes. 49. An examination of convenient procedures for the generation of borane and monoalkyl- and dialkylboranes from lithium borohydride and monoalkyl- and dialkylborohydrides. Organometallics. 5(11). 2303–2307. 15 indexed citations
11.
Rothwell, Arlene P., Karl V. Wood, Morris Srebnik, & Thomas E. Cole. (1986). A mass spectral study of selected isopropyl borinic esters. Organic Mass Spectrometry. 21(3). 165–167. 1 indexed citations
12.
Brown, Herbert C., Thomas E. Cole, Morris Srebnik, & Kee Won Kim. (1986). Hydroboration. 79. Preparation and properties of methylborane and dimethylborane and their characteristics as hydroborating agents. Synthesis of tertiary alcohols containing methyl groups via hydroboration. The Journal of Organic Chemistry. 51(25). 4925–4930. 22 indexed citations
13.
Brown, Herbert C., et al.. (1986). Chiral synthesis via organoboranes. 8. Synthetic utility of boronic esters of essentially 100% optical purity. Synthesis of primary amines of very high enantiomeric purities. Journal of the American Chemical Society. 108(21). 6761–6764. 88 indexed citations
14.
Brown, Herbert C., Morris Srebnik, & Thomas E. Cole. (1986). Organoboranes. 48. Improved procedures for the preparation of boronic and borinic esters. Organometallics. 5(11). 2300–2303. 74 indexed citations
15.
Brown, Herbert C. & Thomas E. Cole. (1985). Organoboranes. 39. Convenient procedures for the preparation of methylboronic acid and trimethylboroxin. Organometallics. 4(5). 816–821. 18 indexed citations
17.
Singaram, Bakthan, Thomas E. Cole, & Herbert C. Brown. (1984). Addition compounds of alkali-metal hydrides. 25. Facile reaction of borinic esters with lithium monoethoxyaluminohydride to form lithium dialkylborohydrides. Organometallics. 3(10). 1520–1523. 15 indexed citations
18.
Brown, Herbert C. & Thomas E. Cole. (1983). Organoboranes. 31. A simple preparation of boronic esters from organolithium reagents and selected trialkoxyboranes. Organometallics. 2(10). 1316–1319. 233 indexed citations
19.
Cole, Thomas E., R. Ramage, Kevin Cann, & R. Pettit. (1980). Homogeneous catalysts for utilization of synthesis gas as a reducing agent. Journal of the American Chemical Society. 102(19). 6182–6184. 57 indexed citations
20.
Swartout, Jeff, et al.. (1964). THE OAK RIDGE HIGH FLUX ISOTOPE REACTOR. OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information).

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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