Victoria A. Doughty

737 total citations
16 papers, 581 citations indexed

About

Victoria A. Doughty is a scholar working on Organic Chemistry, Pharmacology and Biotechnology. According to data from OpenAlex, Victoria A. Doughty has authored 16 papers receiving a total of 581 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Organic Chemistry, 10 papers in Pharmacology and 7 papers in Biotechnology. Recurrent topics in Victoria A. Doughty's work include Chemical synthesis and alkaloids (9 papers), Phytochemistry and Bioactivity Studies (8 papers) and Marine Sponges and Natural Products (7 papers). Victoria A. Doughty is often cited by papers focused on Chemical synthesis and alkaloids (9 papers), Phytochemistry and Bioactivity Studies (8 papers) and Marine Sponges and Natural Products (7 papers). Victoria A. Doughty collaborates with scholars based in United States and United Kingdom. Victoria A. Doughty's co-authors include Amos B. Smith, Ian Paterson, Kiyoshi Nakayama, Linghang Zhuang, Noriaki Murase, Qiyan Lin, Mark D. McBriar, Chris Sfouggatakis, Clay S. Bennett and Malcolm D. McLeod and has published in prestigious journals such as Angewandte Chemie International Edition, Tetrahedron and Organic Letters.

In The Last Decade

Victoria A. Doughty

16 papers receiving 575 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Victoria A. Doughty United States	14	530	224	129	117	69	16	581
Nativitat Valls Spain	13	370 0.7×	105 0.5×	214 1.7×	112 1.0×	58 0.8×	31	551
William H. Moser United States	17	891 1.7×	183 0.8×	157 1.2×	91 0.8×	77 1.1×	22	947
Chris Sfouggatakis United States	12	462 0.9×	130 0.6×	133 1.0×	74 0.6×	36 0.5×	20	542
François‐Hugues Porée France	14	458 0.9×	93 0.4×	140 1.1×	89 0.8×	62 0.9×	30	558
Mizuka Tagashira Japan	8	427 0.8×	95 0.4×	162 1.3×	84 0.7×	50 0.7×	15	544
Jacques P. Ragot Germany	12	402 0.8×	116 0.5×	132 1.0×	119 1.0×	16 0.2×	14	538
Kau-Ming Chen United States	8	435 0.8×	117 0.5×	165 1.3×	142 1.2×	20 0.3×	12	548
Valentin S. Enev Austria	14	399 0.8×	72 0.3×	129 1.0×	102 0.9×	45 0.7×	41	539
Masahiro Miyazawa Japan	18	749 1.4×	96 0.4×	181 1.4×	93 0.8×	33 0.5×	58	815
Zachary G. Brill United States	7	418 0.8×	120 0.5×	174 1.3×	115 1.0×	47 0.7×	9	551

Countries citing papers authored by Victoria A. Doughty

Since Specialization

Citations

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

Fields of papers citing papers by Victoria A. Doughty

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Victoria A. Doughty. 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 Victoria A. Doughty. The network helps show where Victoria A. Doughty may publish in the future.

Co-authorship network of co-authors of Victoria A. Doughty

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

All Works

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16 of 16 papers shown

1.

Paterson, Ian, Victoria A. Doughty, Malcolm D. McLeod, & Thomas Trieselmann. (2011). Stereocontrolled total synthesis of (+)-concanamycin F: the strategic use of boron-mediated aldol reactions of chiral ketones. Tetrahedron. 67(52). 10119–10128. 24 indexed citations

2.

Smith, Amos B., Chris Sfouggatakis, Jeffrey B. Sperry, et al.. (2009). Spongipyran synthetic studies. Evolution of a scalable total synthesis of (+)-spongistatin 1. Tetrahedron. 65(33). 6489–6509. 47 indexed citations

3.

Smith, Amos B., Qiyan Lin, Victoria A. Doughty, et al.. (2009). Spongipyran synthetic studies. Total synthesis of (+)-spongistatin 2. Tetrahedron. 65(33). 6470–6488. 22 indexed citations

4.

Smith, Amos B., Chris Sfouggatakis, Dimitar B. Gotchev, et al.. (2004). Spongistatin Synthetic Studies. Evolution of a Scalable Synthesis for the EF Fragment of (+)-Spongistatin 1 Exploiting a Petasis−Ferrier Union/Rearrangement Tactic. Organic Letters. 6(20). 3637–3640. 31 indexed citations

5.

Smith, Amos B., Wenyu Zhu, Shohei Shirakami, et al.. (2003). Total Synthesis of (+)-Spongistatin 1. An Effective Second-Generation Construction of an Advanced EF Wittig Salt, Fragment Union, and Final Elaboration. Organic Letters. 5(5). 761–764. 54 indexed citations

6.

Smith, Amos B., Victoria A. Doughty, Chris Sfouggatakis, et al.. (2002). Spongistatin Synthetic Studies. An Efficient, Second-Generation Construction of an Advanced ABCD Intermediate. Organic Letters. 4(5). 783–786. 73 indexed citations

7.

Smith, Amos B., Qiyan Lin, Victoria A. Doughty, et al.. (2001). The Spongistatins: Architecturally Complex Natural Products—Part Two: Synthesis of the C(29–51) Subunit, Fragment Assembly, and Final Elaboration to (+)-Spongistatin 2. Angewandte Chemie. 113(1). 202–205. 17 indexed citations

8.

Smith, Amos B., Victoria A. Doughty, Qiyan Lin, et al.. (2001). The Spongistatins: Architecturally Complex Natural Products—Part One: A Formal Synthesis of (+)-Spongistatin 1 by Construction of an Advanced ABCD Fragment. Angewandte Chemie. 113(1). 197–201. 19 indexed citations

9.

Smith, Amos B., Victoria A. Doughty, Qiyan Lin, et al.. (2001). The Spongistatins: Architecturally Complex Natural Products-Part One: A Formal Synthesis of (+)-Spongistatin 1 by Construction of an Advanced ABCD Fragment. Angewandte Chemie International Edition. 40(1). 191–195. 95 indexed citations

10.

Smith, Amos B., Qiyan Lin, Victoria A. Doughty, et al.. (2001). The Spongistatins: Architecturally Complex Natural Products-Part Two: Synthesis of the C(29-51) Subunit, Fragment Assembly, and Final Elaboration to (+)-Spongistatin 2. Angewandte Chemie International Edition. 40(1). 196–199. 86 indexed citations

11.

Smith, Amos B., Victoria A. Doughty, Qiyan Lin, et al.. (2001). The Spongistatins: Architecturally Complex Natural Products-Part One: A Formal Synthesis of (+)-Spongistatin 1 by Construction of an Advanced ABCD Fragment Financial support was provided by the National Institutes of Health (National Cancer Institute) through Grant CA-70329, NIH Postdoctoral Fellowships to A.M.B. and W.H.M., a Japan Society for Promotion of Science Fellowship to N.M., and a Royal Society Fulbright Fellowship to V.A.D. We also thank the Daiichi Pharmaceutical Co., Ltd, and the Tanabe Seiyaku Co., Ltd for financial support. Finally we thank Dr. George T. Furst, Dr. Patrick J. Carroll, Dr. Rakesh Kohli, and Mr John Dykins of the University of Pennsylvania Spectroscopic Service Center for assistance in securing and interpreting high-field NMR spectra, X-ray crystal structures, and mass spectra.. PubMed. 40(1). 191–195. 10 indexed citations

12.

Smith, Amos B., Qiyan Lin, Victoria A. Doughty, et al.. (2001). The Spongistatins: Architecturally Complex Natural Products—Part Two: Synthesis of the C(29–51) Subunit, Fragment Assembly, and Final Elaboration to (+)-Spongistatin 2. Angewandte Chemie International Edition. 40(1). 196–199. 1 indexed citations

13.

Smith, Amos B., Qiyan Lin, Victoria A. Doughty, et al.. (2001). The Spongistatins: Architecturally Complex Natural Products-Part Two: Synthesis of the C(29-51) Subunit, Fragment Assembly, and Final Elaboration to (+)-Spongistatin 2 Financial support was provided by the National Institutes of Health (National Cancer Institute) through Grant CA-70329, a NIH Postdoctoral Fellowship to C.S.B., a Japan Society for Promotion of Science Fellowship to N.M., and a Royal Society Fulbright Fellowship to V.A.D. We also thank the Daiichi Pharmaceutical Co., Ltd, and the Tanabe Seiyaku Co., Ltd for financial support. Finally we thank Dr George T. Furst, Dr. Patrick J. Carroll, and Dr. Rakesh Kohli of the University of Pennsylvania Spectroscopic Service Center for assistance in securing and interpreting high-field NMR spectra, X-ray crystal structures, and mass spectra, respectively.. PubMed. 40(1). 196–199. 23 indexed citations

14.

Paterson, Ian, Victoria A. Doughty, Malcolm D. McLeod, & Thomas Trieselmann. (2000). Total Synthesis of (+)-Concanamycin F. Angewandte Chemie International Edition. 39(7). 1308–1312. 41 indexed citations

15.

Paterson, Ian, Victoria A. Doughty, Malcolm D. McLeod, & Thomas Trieselmann. (2000). Total Synthesis of (+)-Concanamycin F. Angewandte Chemie. 112(7). 1364–1368. 13 indexed citations

16.

Paterson, Ian & Victoria A. Doughty. (1999). anti-Aldol reactions of lactate-derived ketones. Application to the synthesis of (−)-tetrahydrolipstatin. Tetrahedron Letters. 40(2). 393–394. 25 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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