David R. Kronenthal

1.1k total citations
24 papers, 791 citations indexed

About

David R. Kronenthal is a scholar working on Organic Chemistry, Molecular Biology and Spectroscopy. According to data from OpenAlex, David R. Kronenthal has authored 24 papers receiving a total of 791 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Organic Chemistry, 11 papers in Molecular Biology and 5 papers in Spectroscopy. Recurrent topics in David R. Kronenthal's work include Chemical Synthesis and Analysis (7 papers), Asymmetric Synthesis and Catalysis (7 papers) and Synthetic Organic Chemistry Methods (5 papers). David R. Kronenthal is often cited by papers focused on Chemical Synthesis and Analysis (7 papers), Asymmetric Synthesis and Catalysis (7 papers) and Synthetic Organic Chemistry Methods (5 papers). David R. Kronenthal collaborates with scholars based in United States, Germany and Sweden. David R. Kronenthal's co-authors include Richard H. Mueller, Thomas P. Kissick, Janak Singh, Helen Y. Chen, Annie Pullockaran, Steven H. Spergel, Joel C. Barrish, Lilian Radesca, Helen Y. Wu and Ming‐Hsing Huang and has published in prestigious journals such as Angewandte Chemie International Edition, The Journal of Organic Chemistry and Tetrahedron.

In The Last Decade

David R. Kronenthal

23 papers receiving 748 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David R. Kronenthal United States 15 624 293 92 74 44 24 791
Jeffrey A. McKie United States 16 868 1.4× 323 1.1× 92 1.0× 75 1.0× 48 1.1× 18 1.0k
Sivappa Rasapalli United States 19 792 1.3× 231 0.8× 61 0.7× 97 1.3× 36 0.8× 49 925
Yoko Yuasa Japan 14 567 0.9× 198 0.7× 74 0.8× 41 0.6× 56 1.3× 76 661
Denice M. Spero United States 17 756 1.2× 237 0.8× 114 1.2× 135 1.8× 69 1.6× 26 975
Jean‐François Poisson France 21 780 1.3× 362 1.2× 77 0.8× 54 0.7× 41 0.9× 56 1.0k
Matthew M. Abelman United States 16 894 1.4× 186 0.6× 65 0.7× 79 1.1× 48 1.1× 24 1.0k
Daqiang Xu United States 15 710 1.1× 215 0.7× 129 1.4× 49 0.7× 19 0.4× 27 868
Jean‐Louis Gras France 14 548 0.9× 224 0.8× 44 0.5× 56 0.8× 32 0.7× 40 669
Luca Parlanti Italy 10 805 1.3× 215 0.7× 87 0.9× 89 1.2× 13 0.3× 18 925
Yuan‐Ping Ruan China 23 1.1k 1.8× 337 1.2× 123 1.3× 79 1.1× 22 0.5× 45 1.2k

Countries citing papers authored by David R. Kronenthal

Since Specialization
Citations

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

Fields of papers citing papers by David R. Kronenthal

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David R. Kronenthal. 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 David R. Kronenthal. The network helps show where David R. Kronenthal may publish in the future.

Co-authorship network of co-authors of David R. Kronenthal

This figure shows the co-authorship network connecting the top 25 collaborators of David R. Kronenthal. A scholar is included among the top collaborators of David R. Kronenthal 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 David R. Kronenthal. David R. Kronenthal 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.
Shi, Zhongping, Junying Fan, David R. Kronenthal, & Boguslaw Mudryk. (2018). Development of a Practical Synthesis of a Farnesyltransferase Inhibitor. Organic Process Research & Development. 22(11). 1534–1540. 2 indexed citations
2.
Ortiz, Adrian, Tamas Benkovics, Gregory L. Beutner, et al.. (2015). Scalable Synthesis of the Potent HIV Inhibitor BMS‐986001 by Non‐Enzymatic Dynamic Kinetic Asymmetric Transformation (DYKAT). Angewandte Chemie International Edition. 54(24). 7185–7188. 45 indexed citations
3.
Ramı́rez, Antonio, Michael J. Lawler, Yun K. Ye, et al.. (2014). The Effect of Additives on the Zinc Carbenoid-Mediated Cyclopropanation of a Dihydropyrrole. The Journal of Organic Chemistry. 79(13). 6233–6243. 8 indexed citations
4.
Radesca, Lilian, et al.. (2004). One-Carbon Chain Extension of Esters to α-Chloroketones:  A Safer Route without Diazomethane. The Journal of Organic Chemistry. 69(5). 1629–1633. 56 indexed citations
5.
Yu, Jurong, Jeffrey S. DePue, & David R. Kronenthal. (2004). Synthesis of (±)-camptothecin using a [3+2] nitrone cycloaddition to construct the CDE ring moiety. Tetrahedron Letters. 45(39). 7247–7250. 12 indexed citations
6.
Xu, Zhongmin, Janak Singh, Thomas P. Kissick, et al.. (2002). Process Research and Development for an Efficient Synthesis of the HIV Protease Inhibitor BMS-232632. Organic Process Research & Development. 6(3). 323–328. 46 indexed citations
7.
Qian, Xinhua, et al.. (2002). A Stereoselective Synthesis of BMS-262084, an Azetidinone-Based Tryptase Inhibitor. The Journal of Organic Chemistry. 67(11). 3595–3600. 22 indexed citations
8.
Singh, Ambarish K., et al.. (2002). A Practical Synthesis of l-Valyl-pyrrolidine-(2R)-boronic Acid:  Efficient Recycling of the Costly Chiral Auxiliary (+)-Pinanediol. Organic Process Research & Development. 6(6). 814–816. 15 indexed citations
9.
Goswami, Animesh, J. M. Howell, Maxime Soumeillant, et al.. (2001). Chemical and Enzymatic Resolution of (R,S)-N-(tert-Butoxycarbonyl)-3-hydroxymethylpiperidine. Organic Process Research & Development. 5(4). 415–420. 12 indexed citations
10.
11.
Hanson, Ronald L., Amit Banerjee, David B. Brzozowski, et al.. (1999). Enzymatic synthesis of l-6-hydroxynorleucine. Bioorganic & Medicinal Chemistry. 7(10). 2247–2252. 54 indexed citations
12.
Kronenthal, David R., et al.. (1995). Synthesis of 6-Cyano-2,2-dimethyl-2H-1-benzopyran and Other Substituted 2,2-Dimethyl-2H-1-benzopyrans. The Journal of Organic Chemistry. 60(11). 3397–3400. 48 indexed citations
13.
Patel, Ramesh N., Amit Banerjee, Brian J. Davis, et al.. (1994). Stereoselective epoxidation of 2,2-dimethyl-2H-1- benzopyran-6-carbonitrile. Bioorganic & Medicinal Chemistry. 2(6). 535–542. 14 indexed citations
14.
Kronenthal, David R., et al.. (1993). A novel and highly efficient desymmetrization of a meso-anhydride by a chiral grignard reagent. Tetrahedron Letters. 34(50). 8063–8066. 25 indexed citations
15.
Das, Jagabandhu, et al.. (1992). Novel methods for syntheses of substituted oxazoles by cyclization of vinyl bromides. Tetrahedron Letters. 33(51). 7835–7838. 26 indexed citations
16.
Kronenthal, David R., et al.. (1990). Stereospecific friedel-crafts alkylation of benzene with 4-mesyloxy-L-prolines. A new synthesis of 4-phenylprolines. Tetrahedron Letters. 31(9). 1241–1244. 33 indexed citations
17.
SLUSARCHYK, W. A., Tamara Dejneka, Jack Z. Gougoutas, et al.. (1986). β-Lactam synthesis: Chemospecific sulfonation and cyclization of the β-hydroxyvaline nucleus. Tetrahedron Letters. 27(25). 2789–2792. 18 indexed citations
18.
CIMARUSTI, C. M., D P Bonner, H. Breuer, et al.. (1983). 4-Alkylated monobactams. Tetrahedron. 39(15). 2577–2589. 43 indexed citations
19.
Kronenthal, David R., et al.. (1982). Oxidative N-dearylation of 2-azetidinones. p-Anisidine as a source of azetidinone nitrogen. The Journal of Organic Chemistry. 47(14). 2765–2768. 218 indexed citations
20.
Kronenthal, David R., et al.. (1978). Reactions of derivatives of 1,2,3-triphenylcyclopropene with iron salts. The Journal of Organic Chemistry. 43(2). 232–238.

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