Andrew G. Brewster

637 total citations
26 papers, 386 citations indexed

About

Andrew G. Brewster is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, Andrew G. Brewster has authored 26 papers receiving a total of 386 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Organic Chemistry, 8 papers in Molecular Biology and 4 papers in Pharmacology. Recurrent topics in Andrew G. Brewster's work include Asymmetric Synthesis and Catalysis (8 papers), Chemical Synthesis and Analysis (7 papers) and Synthetic Organic Chemistry Methods (6 papers). Andrew G. Brewster is often cited by papers focused on Asymmetric Synthesis and Catalysis (8 papers), Chemical Synthesis and Analysis (7 papers) and Synthetic Organic Chemistry Methods (6 papers). Andrew G. Brewster collaborates with scholars based in United Kingdom. Andrew G. Brewster's co-authors include Mark G. Moloney, Mark D. Andrews, Steven V. Ley, D. H. R. BARTON, George R. Brown, Michael J. Smithers, D.J. Watkin, Keith Prout, Alan J. Foubister and Thomas G. Back and has published in prestigious journals such as Chemical Communications, Journal of Medicinal Chemistry and Tetrahedron.

In The Last Decade

Andrew G. Brewster

26 papers receiving 375 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andrew G. Brewster United Kingdom 12 306 120 90 46 35 26 386
W. J. Sipio United States 7 237 0.8× 58 0.5× 54 0.6× 73 1.6× 42 1.2× 10 313
James K. Sutherland United Kingdom 14 381 1.2× 171 1.4× 91 1.0× 23 0.5× 25 0.7× 56 519
PS Rutledge New Zealand 11 299 1.0× 177 1.5× 68 0.8× 71 1.5× 25 0.7× 82 488
R. Gericke Germany 9 340 1.1× 162 1.4× 107 1.2× 18 0.4× 36 1.0× 15 526
Heinrich Meier Germany 13 221 0.7× 279 2.3× 86 1.0× 23 0.5× 52 1.5× 21 582
Y. ISOMURA Japan 12 276 0.9× 197 1.6× 70 0.8× 110 2.4× 20 0.6× 25 506
Margaret Y. Chu‐Moyer United States 14 486 1.6× 188 1.6× 94 1.0× 11 0.2× 20 0.6× 18 576
Fumio Satoh Japan 12 231 0.8× 161 1.3× 75 0.8× 51 1.1× 10 0.3× 53 417
Kimio Takahashi Japan 10 288 0.9× 74 0.6× 34 0.4× 34 0.7× 16 0.5× 46 361
John Reiner China 13 343 1.1× 206 1.7× 22 0.2× 32 0.7× 29 0.8× 28 533

Countries citing papers authored by Andrew G. Brewster

Since Specialization
Citations

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

Fields of papers citing papers by Andrew G. Brewster

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andrew G. Brewster. 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 Andrew G. Brewster. The network helps show where Andrew G. Brewster may publish in the future.

Co-authorship network of co-authors of Andrew G. Brewster

This figure shows the co-authorship network connecting the top 25 collaborators of Andrew G. Brewster. A scholar is included among the top collaborators of Andrew G. Brewster 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 Andrew G. Brewster. Andrew G. Brewster 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.
Brewster, Andrew G., et al.. (2005). Enantiopure Bicyclic Piperidinones: Stereocontrolled Cycloadditions. Letters in Organic Chemistry. 2(1). 21–24. 1 indexed citations
2.
Brewster, Andrew G., et al.. (2004). Enantiopure bicyclic piperidinones: stereoselectivity in lactam enolate alkylations. Organic & Biomolecular Chemistry. 2(7). 1031–1043. 11 indexed citations
3.
Brewster, Andrew G., et al.. (2004). Enantiopure bicyclic piperidinones: stereocontrolled conjugate additions leading to substituted piperidinones. Organic & Biomolecular Chemistry. 2(12). 1800–1800. 10 indexed citations
4.
Brewster, Andrew G., et al.. (2002). Memory of chirality effects in aldol cyclisations of 1-(3-oxobutyryl) derivatives of l-4-oxaproline and l-proline isopropyl esters. Tetrahedron Letters. 43(21). 3919–3922. 19 indexed citations
5.
Bailey, Patrick D., Simon R. L. Everitt, Keith M. Morgan, & Andrew G. Brewster. (2001). The asymmetric synthesis and conformational analysis of new C 2 -symmetric macrocycles derived from head-to-head linked α -amino acids and benzene or pyridine. Tetrahedron. 57(7). 1379–1386. 10 indexed citations
6.
Andrews, Mark D., Andrew G. Brewster, & Mark G. Moloney. (2001). Diastereocontrolled synthesis of hydroxylated lactams. Journal of the Chemical Society Perkin Transactions 1. 80–90. 1 indexed citations
7.
Andrews, Mark D., et al.. (1998). Regioselective Dieckmann cyclisations leading to enantiopure highly functionalised tetramic acid derivatives. Journal of the Chemical Society Perkin Transactions 1. 223–236. 54 indexed citations
8.
Andrews, Mark D., et al.. (1997). A Short Synthesis of an Enantiopure Benzo[e]isoindolinone. Synthesis. 1997(3). 305–308. 8 indexed citations
9.
10.
Brewster, Andrew G., et al.. (1995). ChemInform Abstract: A Concise Approach to Functionalized Homochiral Tetramic Acids.. ChemInform. 26(3). 1 indexed citations
11.
Brewster, Andrew G., et al.. (1995). Dual-Acting Thromboxane Receptor Antagonist/Synthase Inhibitors: Synthesis and Biological Properties of [2-Substituted-4-(3-pyridyl)-1,3-dioxan-5-yl]alkenoic Acids. Journal of Medicinal Chemistry. 38(4). 686–694. 21 indexed citations
12.
Brewster, Andrew G., George R. Brown, David S. Clarke, et al.. (1995). A Novel Approach to Dual-Acting Thromboxane Receptor Antagonist/Synthase Inhibitors Based on the Link of 1,3-Dioxane-Thromboxane Receptor Antagonists and -Thromboxane Synthase Inhibitors. Journal of Medicinal Chemistry. 38(10). 1608–1628. 26 indexed citations
13.
Andrews, Mark D., Andrew G. Brewster, & Mark G. Moloney. (1994). A concise approach to functionalised, homochiral tetramic acids. Tetrahedron Asymmetry. 5(8). 1477–1478. 15 indexed citations
14.
Sutherland, James K., et al.. (1988). Synthetic approaches to thiathromboxanes. Part 2. Synthesis of structural isomers of thiathromboxane A2. Journal of the Chemical Society Perkin Transactions 1. 675–675. 14 indexed citations
15.
Brewster, Andrew G., et al.. (1988). The synthesis of a novel thromboxane receptor antagonis 4(Z)-6-(2--chlorophenyl-4--hydroxyphenyl-1,3-dioxan--5-yl) hexenoic acid ICI 192605. Prostaglandins. 36(2). 173–178. 26 indexed citations
16.
Brewster, Andrew G., et al.. (1986). 6- vs 7- Ring selectivity during acetal formation. Tetrahedron Letters. 27(22). 2539–2542. 6 indexed citations
17.
BARTON, D. H. R., et al.. (1981). Oxidation of phenols, pyrocatechols, and hydroquinones to ortho-quinones using benzeneseleninic anhydride. Journal of the Chemical Society Perkin Transactions 1. 1473–1473. 25 indexed citations
18.
Barton, Derek H. R., Andrew G. Brewster, R. Hui, et al.. (1978). Oxidation of alcohols using benzeneseleninic anhydride. Journal of the Chemical Society Chemical Communications. 952–952. 40 indexed citations
19.
Brewster, Andrew G., et al.. (1977). X-Ray evidence for partial bonding between sulphur or selenium and oxygen in thio- and seleno-imines. Journal of the Chemical Society Chemical Communications. 325–325. 9 indexed citations
20.
BARTON, D. H. R., et al.. (1976). Oxidation of phenols to ortho-quinones using diphenylseleninic anhydride. Journal of the Chemical Society Chemical Communications. 985–985. 22 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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