William O. Moss

716 total citations
24 papers, 508 citations indexed

About

William O. Moss is a scholar working on Organic Chemistry, Molecular Biology and Pharmaceutical Science. According to data from OpenAlex, William O. Moss has authored 24 papers receiving a total of 508 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Organic Chemistry, 10 papers in Molecular Biology and 3 papers in Pharmaceutical Science. Recurrent topics in William O. Moss's work include Chemical Synthesis and Analysis (7 papers), Synthesis of heterocyclic compounds (5 papers) and Chemical Synthesis and Reactions (5 papers). William O. Moss is often cited by papers focused on Chemical Synthesis and Analysis (7 papers), Synthesis of heterocyclic compounds (5 papers) and Chemical Synthesis and Reactions (5 papers). William O. Moss collaborates with scholars based in United Kingdom, Singapore and Poland. William O. Moss's co-authors include Edwin Vedējs, Anthony R. Haight, Jonathan D. Moseley, Jonathan R. Reeves, Alan Armstrong, Timothy Gallagher, Stephen G. Davies, Neil J. Hales, Steven D. Bull and Robert H. Bradbury and has published in prestigious journals such as Journal of the American Chemical Society, Chemical Communications and Tetrahedron.

In The Last Decade

William O. Moss

24 papers receiving 483 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
William O. Moss United Kingdom 14 456 131 72 27 26 24 508
N. Bhanumathi India 14 400 0.9× 146 1.1× 74 1.0× 34 1.3× 33 1.3× 25 459
Florence Charbonnier France 11 354 0.8× 98 0.7× 52 0.7× 29 1.1× 55 2.1× 13 426
Yoshihiro Yoshida Japan 10 411 0.9× 155 1.2× 38 0.5× 24 0.9× 28 1.1× 18 478
Wilford L. Mendelson United States 11 268 0.6× 108 0.8× 53 0.7× 38 1.4× 32 1.2× 26 354
Takayuki Tsuritani Japan 15 505 1.1× 109 0.8× 52 0.7× 16 0.6× 15 0.6× 22 531
A. S. Gybin Russia 12 411 0.9× 64 0.5× 49 0.7× 20 0.7× 18 0.7× 21 457
D. Seebach Germany 6 387 0.8× 146 1.1× 54 0.8× 20 0.7× 48 1.8× 12 472
Denis Har Switzerland 14 328 0.7× 164 1.3× 69 1.0× 12 0.4× 36 1.4× 21 415
Joel Slade Switzerland 12 304 0.7× 134 1.0× 79 1.1× 20 0.7× 33 1.3× 17 372
Carlos Alvarez‐Ibarra Spain 15 513 1.1× 157 1.2× 82 1.1× 16 0.6× 41 1.6× 51 562

Countries citing papers authored by William O. Moss

Since Specialization
Citations

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

Fields of papers citing papers by William O. Moss

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by William O. Moss. 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 William O. Moss. The network helps show where William O. Moss may publish in the future.

Co-authorship network of co-authors of William O. Moss

This figure shows the co-authorship network connecting the top 25 collaborators of William O. Moss. A scholar is included among the top collaborators of William O. Moss 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 William O. Moss. William O. Moss 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
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Moseley, Jonathan D. & William O. Moss. (2002). A New Approach to Rapid Parallel Development for Four Neurokinin Antagonists. Part 1.. Organic Process Research & Development. 7(1). 53–57. 7 indexed citations
4.
Ashworth, Ian W., et al.. (2002). A New Route for Manufacture of 3-Cyano-1-naphthalenecarboxylic Acid. Organic Process Research & Development. 7(1). 74–81. 34 indexed citations
5.
Moseley, Jonathan D., et al.. (2002). A New Approach to Rapid Parallel Development of Four Neurokinin Antagonists. Part 2. Synthesis of ZD6021 Cyano Acid. Organic Process Research & Development. 7(1). 58–66. 13 indexed citations
6.
Moss, William O., et al.. (2002). Asymmetric Sulfoxidation of an Aryl Ethyl Sulfide:  Modification of Kagan Procedure to Provide a Viable Manufacturing Process. Organic Process Research & Development. 6(3). 225–229. 28 indexed citations
7.
Parker, Jeremy S., et al.. (2002). A New Approach to the Rapid Parallel Development of Four Neurokinin Antagonists. Part 3. Assembly of Neurokinin Antagonists. Organic Process Research & Development. 7(1). 67–73. 12 indexed citations
8.
Armstrong, Alan, William O. Moss, & Jonathan R. Reeves. (2001). Asymmetric epoxidation catalyzed by esters of α-hydroxy-8-oxabicyclo[3.2.1]octan-3-one. Tetrahedron Asymmetry. 12(20). 2779–2781. 24 indexed citations
9.
Moseley, Jonathan D., et al.. (2001). Investigation of an Alternative Route to ZD3638 and Cost-Benefit Analysis Comparison of Raw Materials with the Previous Route. Organic Process Research & Development. 5(5). 491–497. 19 indexed citations
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Bull, Steven D., et al.. (1998). Asymmetric synthesis of (2R,5R)-2,5-diaminohexan-1,6-dioic acid. Tetrahedron. 54(35). 10379–10388. 10 indexed citations
12.
Bull, Steven D., Stephen G. Davies, & William O. Moss. (1998). Practical synthesis of Schöllkopf's bis-lactim ether chiral auxiliary: (3S)-3,6-dihydro-2,5-dimethoxy-3-isopropyl-pyrazine. Tetrahedron Asymmetry. 9(2). 321–327. 33 indexed citations
13.
Vedējs, Edwin & William O. Moss. (1993). Lithiated aziridine reagents. Journal of the American Chemical Society. 115(4). 1607–1608. 41 indexed citations
14.
Moss, William O., Mary F. Mahon, Kieran C. Molloy, et al.. (1992). 2-Amino ketene S,S-acetals as α-amino acid homoenolate equivalents. Synthesis of 3-substituted prolines and molecular structure of 2-(N-pivaloylpyrrolidin-2-ylidene)-1,3-dithiane. Journal of the Chemical Society Perkin Transactions 1. 2615–2624. 13 indexed citations
15.
Vedējs, Edwin, Anthony R. Haight, & William O. Moss. (1992). Internal coordination at tin promotes selective alkyl transfer in the Stille coupling reaction. Journal of the American Chemical Society. 114(16). 6556–6558. 116 indexed citations
16.
Moss, William O., Robert H. Bradbury, Neil J. Hales, & Timothy Gallagher. (1992). Ketene S,S-acetals as 1,3-dipolarophiles: application to the synthesis of polyhydroxylated pyrrolidines. Journal of the Chemical Society Perkin Transactions 1. 1901–1901. 9 indexed citations
17.
Moss, William O., Robert H. Bradbury, Neil J. Hales, & Timothy Gallagher. (1990). Ketene dithioacetals as 1,3-dipolarophiles. Applications to the synthesis of cyclic amino acids. Journal of the Chemical Society Chemical Communications. 51–51. 11 indexed citations
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Moss, William O., Robert H. Bradbury, Neil J. Hales, & Timothy Gallagher. (1988). Ketene-S,S-acetals as 1,3-dipolarophiles. Reactivity towards electron-deficient azides.. Tetrahedron Letters. 29(49). 6475–6478. 9 indexed citations
20.
Karr, Dane E., W F Bibb, & William O. Moss. (1982). Isoprenoid Quinones oftheGenusLegionella. 3 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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