Acyl anion free N-heterocyclic carbene organocatalysis SJ Ryan, L Candish, DW Lupton Chemical Society Reviews 42 (12), 4906-4917, 2013 | 796 | 2013 |
N-Heterocyclic Carbene-Catalyzed Generation of α,β-Unsaturated Acyl Imidazoliums: Synthesis of Dihydropyranones by their Reaction with Enolates SJ Ryan, L Candish, DW Lupton Journal of the American Chemical Society 131 (40), 14176-14177, 2009 | 310 | 2009 |
NMR chemical shifts of trace impurities: Industrially preferred solvents used in process and green chemistry NR Babij, EO McCusker, GT Whiteker, B Canturk, N Choy, LC Creemer, ... Organic process research & development 20 (3), 661-667, 2016 | 261 | 2016 |
N-heterocyclic carbene-catalyzed (4+ 2) cycloaddition/decarboxylation of silyl dienol ethers with α, β-unsaturated acid fluorides SJ Ryan, L Candish, DW Lupton Journal of the American Chemical Society 133 (13), 4694-4697, 2011 | 224 | 2011 |
Co-occurrence of celiac disease and other autoimmune diseases in celiacs and their first-degree relatives SL Neuhausen, L Steele, S Ryan, M Mousavi, M Pinto, KE Osann, ... Journal of autoimmunity 31 (2), 160-165, 2008 | 184 | 2008 |
Acyl azolium fluorides for room temperature nucleophilic aromatic fluorination of chloro-and nitroarenes SJ Ryan, SD Schimler, DC Bland, MS Sanford Organic letters 17 (8), 1866-1869, 2015 | 103 | 2015 |
Synthetic and Quantum Mechanical Studies into the N-Heterocyclic Carbene Catalyzed (4 + 2) Cycloaddition SJ Ryan, A Stasch, MN Paddon-Row, DW Lupton The Journal of Organic Chemistry 77 (2), 1113-1124, 2012 | 92 | 2012 |
Anhydrous Tetramethylammonium Fluoride for Room-Temperature SNAr Fluorination SD Schimler, SJ Ryan, DC Bland, JE Anderson, MS Sanford The Journal of organic chemistry 80 (24), 12137-12145, 2015 | 87 | 2015 |
Predation by Myxococcus xanthus induces Bacillus subtilis to form spore-filled megastructures S Müller, SN Strack, SE Ryan, DB Kearns, JR Kirby Applied and environmental microbiology 81 (1), 203-210, 2015 | 80 | 2015 |
Multiple Approaches to the In Situ Generation of Anhydrous Tetraalkylammonium Fluoride Salts for SNAr Fluorination Reactions MA Cismesia, SJ Ryan, DC Bland, MS Sanford The Journal of Organic Chemistry 82 (10), 5020-5026, 2017 | 65 | 2017 |
Australia’s NRM governance system: Foundations and principles for meeting future challenges S Ryan, K Broderick, Y Sneddon, K Andrews Australian Regional NRM Chairs, Canberra, 2010 | 54 | 2010 |
Identification of functions affecting predator-prey interactions between Myxococcus xanthus and Bacillus subtilis S Müller, SN Strack, SE Ryan, M Shawgo, A Walling, S Harris, ... Journal of bacteriology 198 (24), 3335-3344, 2016 | 43 | 2016 |
1, 3-Dipolar cycloaddition of unstabilised azomethine ylides by Lewis base catalysis S Pandiancherri, SJ Ryan, DW Lupton Organic & Biomolecular Chemistry 10 (39), 7903-7911, 2012 | 41 | 2012 |
The shared water resources of the Murray-Darling Basin M Kirby, R Evans, G Walker, R Cresswell, J Coram, S Khan, Z Paydar, ... Murray-Darling Basin Commission, Canberra, 2006 | 35 | 2006 |
Organocatalyzed [3+ 3] Annulations for the Construction of Heterocycles Y Zhu, Y Huang Synthesis 52 (08), 1181-1202, 2020 | 24 | 2020 |
Governing community-based natural resource management in Australia: International Implications A Dale, K Vella, S Ryan, K Broderick, R Hill, R Potts, T Brewer Land 9 (7), 234, 2020 | 22 | 2020 |
Synthesis of secondary and tertiary amides without coupling agents from amines and potassium acyltrifluoroborates (KATs) A Schuhmacher, T Shiro, SJ Ryan, JW Bode Chemical Science 11 (29), 7609-7614, 2020 | 17 | 2020 |
Reagent-free continuous thermal tert-butyl ester deprotection KP Cole, SJ Ryan, JMC Groh, RD Miller Bioorganic & Medicinal Chemistry 25 (23), 6209-6217, 2017 | 17 | 2017 |
N-Heterocyclic Carbene (NHC)-Catalyzed All-Carbon [4+ 2] Cycloaddition-Decarboxylation S Ryan, L Candish, DW Lupton Synlett 2011 (16), 2275-2278, 2011 | 16 | 2011 |
Catalytic synthesis of potassium acyltrifluoroborates (KATs) from boronic acids and the thioimidate KAT transfer reagent A Schuhmacher, SJ Ryan, JW Bode Angewandte Chemie International Edition 60 (8), 3918-3922, 2021 | 14 | 2021 |