Sandra M. King

526 total citations
9 papers, 444 citations indexed

About

Sandra M. King is a scholar working on Organic Chemistry, Pharmacology and Biochemistry. According to data from OpenAlex, Sandra M. King has authored 9 papers receiving a total of 444 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Organic Chemistry, 6 papers in Pharmacology and 3 papers in Biochemistry. Recurrent topics in Sandra M. King's work include Chemical synthesis and alkaloids (7 papers), Alkaloids: synthesis and pharmacology (6 papers) and Traditional and Medicinal Uses of Annonaceae (3 papers). Sandra M. King is often cited by papers focused on Chemical synthesis and alkaloids (7 papers), Alkaloids: synthesis and pharmacology (6 papers) and Traditional and Medicinal Uses of Annonaceae (3 papers). Sandra M. King collaborates with scholars based in United States. Sandra M. King's co-authors include Seth B. Herzon, Xiaoshen Ma and Stephen L. Buchwald and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and The Journal of Organic Chemistry.

In The Last Decade

Sandra M. King

9 papers receiving 438 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sandra M. King United States	9	394	112	70	58	54	9	444
Emma H. Southgate United States	6	640 1.6×	106 0.9×	46 0.7×	98 1.7×	39 0.7×	6	718
Solymar Negretti United States	7	522 1.3×	179 1.6×	52 0.7×	81 1.4×	36 0.7×	7	637
Dongshun Ni China	11	417 1.1×	41 0.4×	47 0.7×	32 0.6×	19 0.4×	17	453
Daniel J. Tao United States	5	433 1.1×	81 0.7×	44 0.6×	72 1.2×	36 0.7×	5	485
Daniel J. Mack United States	9	473 1.2×	76 0.7×	32 0.5×	109 1.9×	16 0.3×	13	572
Emílio C. de Lucca Brazil	11	311 0.8×	112 1.0×	22 0.3×	41 0.7×	20 0.4×	18	364
Dexter C. Davis United States	8	362 0.9×	52 0.5×	30 0.4×	58 1.0×	43 0.8×	13	414
Shogo Kamo Japan	9	221 0.6×	46 0.4×	31 0.4×	57 1.0×	71 1.3×	32	313
Huaiji Zheng China	16	610 1.5×	44 0.4×	46 0.7×	72 1.2×	51 0.9×	35	666
Sarah E. Wengryniuk United States	14	535 1.4×	84 0.8×	22 0.3×	97 1.7×	54 1.0×	30	607

Countries citing papers authored by Sandra M. King

Since Specialization

Citations

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

Fields of papers citing papers by Sandra M. King

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sandra M. King. 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 Sandra M. King. The network helps show where Sandra M. King may publish in the future.

Co-authorship network of co-authors of Sandra M. King

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

All Works

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9 of 9 papers shown

1.

King, Sandra M. & Stephen L. Buchwald. (2016). Development of a Method for the N-Arylation of Amino Acid Esters with Aryl Triflates. Organic Letters. 18(16). 4128–4131. 58 indexed citations

2.

King, Sandra M., Xiaoshen Ma, & Seth B. Herzon. (2014). A Method for the Selective Hydrogenation of Alkenyl Halides to Alkyl Halides. Journal of the American Chemical Society. 136(19). 6884–6887. 154 indexed citations

3.

King, Sandra M. & Seth B. Herzon. (2014). Substrate-Modified Functional Group Reactivity: Hasubanan and Acutumine Alkaloid Syntheses. The Journal of Organic Chemistry. 79(19). 8937–8947. 19 indexed citations

4.

King, Sandra M. & Seth B. Herzon. (2013). The Hasubanan and Acutumine Alkaloids. PubMed. 73. 161–222. 17 indexed citations

5.

King, Sandra M., et al.. (2013). Total Syntheses of (−)‐Acutumine and (−)‐Dechloroacutumine. Angewandte Chemie International Edition. 52(13). 3642–3645. 58 indexed citations

6.

King, Sandra M., et al.. (2013). Total Syntheses of (−)‐Acutumine and (−)‐Dechloroacutumine. Angewandte Chemie. 125(13). 3730–3733. 22 indexed citations

7.

King, Sandra M., et al.. (2013). Development of Enantioselective Synthetic Routes to the Hasubanan and Acutumine Alkaloids. The Journal of Organic Chemistry. 78(20). 10031–10057. 41 indexed citations

8.

Herzon, Seth B., et al.. (2011). Efficient Entry to the Hasubanan Alkaloids: First Enantioselective Total Syntheses of (−)‐Hasubanonine, (−)‐Runanine, (−)‐Delavayine, and (+)‐Periglaucine B. Angewandte Chemie International Edition. 50(38). 8863–8866. 57 indexed citations

9.

Herzon, Seth B., et al.. (2011). Efficient Entry to the Hasubanan Alkaloids: First Enantioselective Total Syntheses of (−)‐Hasubanonine, (−)‐Runanine, (−)‐Delavayine, and (+)‐Periglaucine B. Angewandte Chemie. 123(38). 9025–9028. 18 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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