| Year |
Citation |
Score |
| 2023 |
Nakano Y, Maddigan-Wyatt JT, Lupton DW. Enantioselective Catalysis by the Umpolung of Conjugate Acceptors Involving N-Heterocyclic Carbene or Organophosphine 1,4-Addition. Accounts of Chemical Research. PMID 37093247 DOI: 10.1021/acs.accounts.3c00063 |
0.373 |
|
| 2022 |
Cromwell S, Sutio R, Zhang C, Such GK, Lupton DW. Lewis Base Catalyzed Synthesis of Sulfur Heterocycles via the C1-Pyridinium Enolate.*. Angewandte Chemie (International Ed. in English). PMID 35718884 DOI: 10.1002/anie.202206647 |
0.393 |
|
| 2022 |
Maddigan-Wyatt JT, Cao J, Ametovski J, Hooper JF, Lupton DW. Enantioselective Synthesis of Pyrrolidines by a Phosphine-Catalyzed γ-Umpolung/β-Umpolung Cascade. Organic Letters. 24: 2847-2852. PMID 35404624 DOI: 10.1021/acs.orglett.2c00785 |
0.397 |
|
| 2021 |
Pitchumani V, Breugst M, Lupton DW. Enantioselective Rauhut-Currier Reaction with β-Substituted Acrylamides Catalyzed by N-Heterocyclic Carbenes. Organic Letters. 23: 9413-9418. PMID 34842439 DOI: 10.1021/acs.orglett.1c03554 |
0.408 |
|
| 2021 |
Maddigan-Wyatt JT, Blyth MT, Ametovski J, Coote ML, Hooper JF, Lupton DW. Redox Isomerization/(3+2) Allenoate Annulation by Auto-Tandem Phosphine Catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). 27: 16232-16236. PMID 34596926 DOI: 10.1002/chem.202103224 |
0.367 |
|
| 2020 |
Pimparkar S, Bhattacharya T, Maji A, Saha A, Jayarajan R, Dutta U, Lu G, Lupton DW, Maiti D. Para-Selective Cyanation of Arenes by H-Bonded Template. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32196777 DOI: 10.1002/Chem.202001368 |
0.746 |
|
| 2020 |
Pitchumani V, Lupton DW. Studies on Thiourea Catalysed Bromocycloetherification and Bromolactonisations Australian Journal of Chemistry. DOI: 10.1071/Ch20184 |
0.456 |
|
| 2020 |
Nguyen XB, Nakano Y, Lupton DW. Polarity Inversion Catalysis by the 1,4-Addition of N-Heterocyclic Carbenes Australian Journal of Chemistry. 73: 1-8. DOI: 10.1071/Ch19550 |
0.463 |
|
| 2020 |
Cao J, Gillard R, Jahanbakhsh A, Breugst M, Lupton DW. Enantioselective N-Heterocyclic Carbene Catalysis via the Acyl Azolium without Exogenous Oxidants Acs Catalysis. DOI: 10.1021/Acscatal.0C02705 |
0.374 |
|
| 2019 |
Matviitsuk A, Greenhalgh MD, Taylor JE, Nguyen XB, Cordes DB, Slawin AMZ, Lupton DW, Smith AD. Unanticipated Silyl Transfer in Enantioselective α,β-Unsaturated Acyl Ammonium Catalysis Using Silyl Nitronates. Organic Letters. PMID 31868371 DOI: 10.1021/Acs.Orglett.9B04404 |
0.46 |
|
| 2019 |
Dutta U, Maiti S, Pimparkar S, Maiti S, Gahan LR, Krenske EH, Lupton DW, Maiti D. Rhodium catalyzed template-assisted distal -C-H olefination. Chemical Science. 10: 7426-7432. PMID 31489165 DOI: 10.1039/C9Sc01824G |
0.745 |
|
| 2019 |
Bae S, Zhang C, Gillard RM, Lupton DW. Enantioselective N-heterocyclic carbene catalyzed bis(enoate) Rauhut-Currier reaction. Angewandte Chemie (International Ed. in English). PMID 31328857 DOI: 10.1002/Anie.201907111 |
0.471 |
|
| 2019 |
Nguyen XB, Nakano Y, Duggan NM, Scott L, Breugst M, Lupton DW. N-Heterocyclic carbene catalyzed (5 + 1) annulations exploiting a vinyl dianion synthon strategy. Angewandte Chemie (International Ed. in English). PMID 31197900 DOI: 10.1002/Anie.201905475 |
0.479 |
|
| 2019 |
Ametovski A, Lupton DW. Enantioselective Total Synthesis of (−)-Δ9-Tetrahydrocannabinol via N-Heterocyclic Carbene Catalysis Organic Letters. 21: 1212-1215. PMID 30726088 DOI: 10.1021/Acs.Orglett.9B00198 |
0.377 |
|
| 2019 |
Fernando JEM, Nakano Y, Zhang C, Lupton DW. Enantioselective N-heterocyclic carbene catalysis exploiting imine umpolung. Angewandte Chemie (International Ed. in English). PMID 30663829 DOI: 10.1002/Anie.201812585 |
0.478 |
|
| 2019 |
Gass IA, Lu J, Ojha R, Asadi M, Lupton DW, Geoghegan BL, Moubaraki B, Martin LL, Bond AM, Murray KS. [FeII(L•)2][TCNQF4•−]2: A Redox-Active Double Radical Salt Australian Journal of Chemistry. 72: 769. DOI: 10.1071/Ch19175 |
0.314 |
|
| 2019 |
Ametovski A, Lupton DW. Enantioselective Total Synthesis of (−)‑Δ9‑Tetrahydrocannabinol via N‑Heterocyclic CarbeneCatalysis Organic Letters. DOI: 10.1021/Acs.Orglett.9B00198.S001 |
0.324 |
|
| 2018 |
Golf H, O'Shea R, Braybrook C, Hutt O, Lupton DW, Hooper JF. RAFT polymer cross-coupling with boronic acids Chemical Science. 9: 7370-7375. PMID 30542540 DOI: 10.1039/C8Sc01862F |
0.3 |
|
| 2018 |
Simpson Q, Sinclair MJG, Lupton DW, Chaplin AB, Hooper JF. Oxidative Cross-Coupling of Boron and Antimony Nucleophiles via Palladium(I). Organic Letters. PMID 30192552 DOI: 10.1021/Acs.Orglett.8B01989 |
0.407 |
|
| 2018 |
Scott L, Nakano Y, Zhang C, Lupton DW. Enantioselective N-heterocyclic carbene catalyzed cyclopentene synthesis via the b-azolium ylide. Angewandte Chemie (International Ed. in English). PMID 29911348 DOI: 10.1002/Anie.201804271 |
0.445 |
|
| 2018 |
Czyz ML, Weragoda GK, Monaghan R, Connell TU, Brzozowski M, Scully AD, Burton J, Lupton DW, Polyzos A. A visible-light photocatalytic thiolation of aryl, heteroaryl and vinyl iodides. Organic & Biomolecular Chemistry. PMID 29431836 DOI: 10.1039/C8Ob00238J |
0.401 |
|
| 2018 |
Gillard RM, Fernando JEM, Lupton D. Enantioselective N-heterocyclic carbene (NHC) catalysis via the dienyl acyl azolium. Angewandte Chemie (International Ed. in English). PMID 29380549 DOI: 10.1002/Anie.201712604 |
0.485 |
|
| 2018 |
Levens A, An F, Fernando JEM, Ofial AR, Lupton DW, Mayr H. Quantification of the Michael-Acceptor Reactivity of α,β-Unsaturated Acyl Azolium Ions Topics in Catalysis. 61: 585-590. DOI: 10.1007/S11244-018-0914-5 |
0.357 |
|
| 2017 |
Ametovski J, Dutta U, Burchill L, Maiti D, Lupton DW, Hooper JF. Phosphine catalysed (5 + 1) annulation of ynone/cinnamates with primary amines. Chemical Communications (Cambridge, England). PMID 29165450 DOI: 10.1039/C7Cc08252E |
0.762 |
|
| 2017 |
Polyzos A, Lupton DW, Czyz M. Auxiliary-Directed C(sp3)-H Arylation by Synergistic Photoredox and Palladium Catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28862367 DOI: 10.1002/Chem.201704045 |
0.432 |
|
| 2017 |
Zhang C, Lupton DW. Enantioselective N-Heterocyclic Carbene Catalyzed Synthesis of Functionalized Indenes. Organic Letters. PMID 28812898 DOI: 10.1021/Acs.Orglett.7B01981 |
0.488 |
|
| 2017 |
Nguyen K, Lupton DW. N-Heterocyclic Carbene-Catalysed Mukaiyama-Michael Reaction and Mukaiyama Aldol/Mukaiyama-Michael Three-Component Coupling Reaction Australian Journal of Chemistry. 70: 436-441. DOI: 10.1071/Ch16566 |
0.469 |
|
| 2017 |
Fernando JEM, Levens A, Moock D, Lupton DW. N-Heterocyclic Carbene Catalyzed Transformylation Synthesis. 49: 3505-3510. DOI: 10.1055/S-0036-1588449 |
0.456 |
|
| 2017 |
Dutta U, Modak A, Bhaskararao B, Bera M, Bag S, Mondal A, Lupton DW, Sunoj RB, Maiti D. Catalytic Arene meta-C–H Functionalization Exploiting a Quinoline-Based Template Acs Catalysis. 7: 3162-3168. DOI: 10.1021/Acscatal.7B00247 |
0.742 |
|
| 2017 |
Zhang C, Hooper JF, Lupton DW. N-Heterocyclic Carbene Catalysis via the α,β-Unsaturated Acyl Azolium Acs Catalysis. 7: 2583-2596. DOI: 10.1021/Acscatal.6B03663 |
0.423 |
|
| 2016 |
Levens A, Ametovski A, Lupton DW. Enantioselective (4+2) Annulation of Donor–Acceptor Cyclobutanes by N-Heterocyclic Carbene Catalysis Angewandte Chemie. 55: 16136-16140. PMID 27891746 DOI: 10.1002/Anie.201609330 |
0.445 |
|
| 2016 |
Levens A, An F, Breugst M, Mayr H, Lupton DW. Influence of the N-Substituents on the Nucleophilicity and Lewis Basicity of N-Heterocyclic Carbenes. Organic Letters. PMID 27434216 DOI: 10.1021/Acs.Orglett.6B01525 |
0.319 |
|
| 2016 |
Dutta U, Lupton DW, Maiti D. Aryl Nitriles from Alkynes Using tert-Butyl Nitrite: Metal-Free Approach to C≡C Bond Cleavage. Organic Letters. PMID 26849380 DOI: 10.1021/Acs.Orglett.6B00147 |
0.752 |
|
| 2016 |
Nakano Y, Lupton DW. Enantioselective N-Heterocyclic Carbene Catalysis by the Umpolung of α,β-Unsaturated Ketones. Angewandte Chemie (International Ed. in English). 55: 3135-9. PMID 26823153 DOI: 10.1002/anie.201510106 |
0.373 |
|
| 2016 |
Levens A, Lupton DW. All-Carbon (4 + 2) Annulations Catalysed by N-Heterocyclic Carbenes Synlett. 13: 415-424. DOI: 10.1055/S-0036-1588109 |
0.494 |
|
| 2016 |
Asadi M, Hooper JF, Lupton DW. Biodiesel synthesis using integrated acid and base catalysis in continuous flow Tetrahedron. 72: 3729-3733. DOI: 10.1016/J.Tet.2016.03.075 |
0.318 |
|
| 2016 |
Candish L, Gillard RM, Fernando JEM, Levens A, Lupton DW. All-carbon N-heterocyclic Carbene-catalyzed (3+2) Annulation using Donor-Acceptor Cyclopropanes Israel Journal of Chemistry. 56: 522-530. DOI: 10.1002/Ijch.201500102 |
0.478 |
|
| 2016 |
Nakano Y, Lupton DW. Enantioselective N-Heterocyclic Carbene Catalysis by the Umpolung of α,β-Unsaturated Ketones Angewandte Chemie - International Edition. 55: 3135-3139. DOI: 10.1002/Anie.201510106 |
0.472 |
|
| 2015 |
Candish L, Levens A, Lupton DW. N-Heterocyclic carbene catalysed redox isomerisation of esters to functionalised benzaldehydes. Chemical Science. 6: 2366-2370. PMID 29308150 DOI: 10.1039/C4Sc03726J |
0.476 |
|
| 2015 |
Dutta U, Deb A, Lupton DW, Maiti D. The regioselective iodination of quinolines, quinolones, pyridones, pyridines and uracil. Chemical Communications (Cambridge, England). PMID 26489708 DOI: 10.1039/C5Cc07799K |
0.733 |
|
| 2015 |
Levens A, Zhang C, Candish L, Forsyth CM, Lupton D. Enantioselective N-Heterocyclic Carbene Catalyzed Diene Regenerative (4 + 2) Annulation. Organic Letters. 17: 5332-5335. PMID 26484753 DOI: 10.1021/Acs.Orglett.5B02693 |
0.525 |
|
| 2015 |
Ungureanu A, Levens A, Candish L, Lupton DW. N-Heterocyclic Carbene Catalyzed Synthesis of δ-Sultones via α,β-Unsaturated Sulfonyl Azolium Intermediates. Angewandte Chemie (International Ed. in English). 54: 11780-4. PMID 26261029 DOI: 10.1002/Anie.201504633 |
0.449 |
|
| 2015 |
Candish L, Lupton DW. Total Synthesis of (−)-7-Deoxyloganin Exploiting N-Heterocyclic Carbene Catalysis with α,β-Unsaturated Enol Esters Strategies and Tactics in Organic Synthesis. 11: 309-334. DOI: 10.1016/B978-0-08-100023-6.00010-5 |
0.441 |
|
| 2014 |
Candish L, Levens A, Lupton DW. Enantioselective all-carbon (4+2) annulation by N-heterocyclic carbene catalysis. Journal of the American Chemical Society. 136: 14397-14400. PMID 25252043 DOI: 10.1021/Ja508542N |
0.451 |
|
| 2014 |
Kowalczyk M, Lupton DW. Cascade olefin isomerization/intramolecular Diels-Alder reaction catalyzed by N-heterocyclic carbenes. Angewandte Chemie (International Ed. in English). 53: 5314-7. PMID 24706584 DOI: 10.1002/anie.201402067 |
0.416 |
|
| 2014 |
Nakano Y, Lupton DW. Palladium[II] catalysed C(sp3)-H oxidation of dimethyl carbamoyl tetrahydrocarbazoles. Chemical Communications. 50: 1757-1760. PMID 24400324 DOI: 10.1039/C3Cc48545E |
0.346 |
|
| 2014 |
Simpson Q, Konrath AR, Lupton DW. Enantioselective Pd-Catalysed Deallylative γ-Lactonisation of Propargyl Carbazolone Allyl Carbonates: Mechanistic Insight into their Decarboxylative Allylation Australian Journal of Chemistry. 67: 1353-1356. DOI: 10.1071/Ch14211 |
0.387 |
|
| 2014 |
Candish L, Nakano Y, Lupton DW. Lewis Base Catalysis of Three n–π* Mediated Reactions with N-Heterocyclic Carbenes (NHCs), Isothioureas, Bicyclic Tertiary Amines, and Electron-Rich Pyridyls Synthesis. 46: 1823-1835. DOI: 10.1055/S-0033-1338653 |
0.483 |
|
| 2014 |
Asadi M, Bonke S, Polyzos A, Lupton DW. Fukuyama Reduction and Integrated Thioesterification/Fukuyama Reduction of Thioesters and Acyl Chlorides Using Continuous Flow Acs Catalysis. 4: 2070-2074. DOI: 10.1021/Cs5004917 |
0.359 |
|
| 2014 |
Kowalczyk M, Lupton DW. Cascade olefin isomerization/intramolecular diels-alder reaction catalyzed by N-heterocyclic carbenes Angewandte Chemie - International Edition. 53: 5314-5317. DOI: 10.1002/Anie.201402067 |
0.502 |
|
| 2013 |
Ngatimin M, Frey R, Levens A, Nakano Y, Kowalczyk MJ, Konstas K, Hutt OE, Lupton D. Iodobenzene-Catalyzed Oxabicyclo[3.2.1]octane and [4.2.1]Nonane Synthesis via Cascade C–O/C–C Formation Organic Letters. 15: 5858-5861. PMID 24191711 DOI: 10.1021/Ol4029308 |
0.507 |
|
| 2013 |
Hierold J, Lupton DW. C–C bond fragmentation by Grob/Eschenmoser reactions, applications in dendrimer synthesis Organic and Biomolecular Chemistry. 11: 6150-6160. PMID 23925375 DOI: 10.1039/C3Ob40800K |
0.483 |
|
| 2013 |
Candish L, Forsyth CM, Lupton D. N‐tert‐Butyl Triazolylidenes: Catalysts for the Enantioselective (3+2) Annulation of α,β‐Unsaturated Acyl Azoliums Angewandte Chemie. 52: 9149-9152. PMID 23852821 DOI: 10.1002/Anie.201304081 |
0.32 |
|
| 2013 |
Ryan SJ, Candish L, Lupton DW. Acyl anion free N-heterocyclic carbene organocatalysis. Chemical Society Reviews. 42: 4906-17. PMID 23403488 DOI: 10.1039/C3Cs35522E |
0.469 |
|
| 2013 |
Gartshore CJ, Lupton D. Enantioselective palladium-catalyzed decarboxylative allylation of carbazolones and indolones: formal synthesis of (+)-kopsihainanine A Angewandte Chemie. 52: 4113-4116. PMID 23362227 DOI: 10.1002/Anie.201209069 |
0.472 |
|
| 2013 |
Candish L, Lupton DW. N-heterocyclic carbene-catalyzed Ireland-Coates Claisen rearrangement: synthesis of functionalized β-lactones. Journal of the American Chemical Society. 135: 58-61. PMID 23244238 DOI: 10.1021/Ja310449K |
0.448 |
|
| 2013 |
Gartshore CJ, Lupton D. Studies on the Enantioselective Synthesis of Carbazolones as Intermediates in Aspidosperma and Kopsia Alkaloid Synthesis Australian Journal of Chemistry. 66: 882-890. DOI: 10.1071/Ch13287 |
0.456 |
|
| 2012 |
Pandiancherri S, Ryan SJ, Lupton DW. 1,3-Dipolar cycloaddition of unstabilised azomethine ylides by Lewis base catalysis. Organic & Biomolecular Chemistry. 10: 7903-11. PMID 22930129 DOI: 10.1039/C2Ob26047F |
0.395 |
|
| 2012 |
Hierold J, Lupton DW. Synthesis of Spirocyclic γ-Lactones by Cascade Beckwith–Dowd Ring Expansion/Cyclization Organic Letters. 14: 3412-3415. PMID 22712543 DOI: 10.1021/Ol301386K |
0.436 |
|
| 2012 |
Ryan SJ, Stasch A, Paddon-Row MN, Lupton DW. Synthetic and quantum mechanical studies into the N-heterocyclic carbene catalyzed (4 + 2) cycloaddition. The Journal of Organic Chemistry. 77: 1113-24. PMID 22148247 DOI: 10.1021/Jo202500K |
0.415 |
|
| 2012 |
Candish L, Lupton DW. N-heterocyclic carbene cascade catalysis: Dual Brønsted/Lewis base rearrangement of cyclopropyl enol esters to dihydropyranones Chemical Science. 3: 380-383. DOI: 10.1039/C1Sc00666E |
0.412 |
|
| 2011 |
Candish L, Lupton DW. Concise formal synthesis of (−)-7-deoxyloganinvia N-heterocyclic carbene catalysed rearrangement of α,β-unsaturated enol esters Organic and Biomolecular Chemistry. 9: 8182-8189. PMID 22024770 DOI: 10.1039/C1Ob05953J |
0.363 |
|
| 2011 |
Ngatimin M, Frey R, Andrews C, Lupton DW, Hutt OE. Iodobenzene catalysed synthesis of spirofurans and benzopyrans by oxidative cyclisation of vinylogous esters Chemical Communications. 47: 11778-11780. PMID 21952527 DOI: 10.1039/C1Cc15015D |
0.392 |
|
| 2011 |
Ryan SJ, Candish L, Lupton DW. N-Heterocyclic carbene-catalyzed (4+2) cycloaddition/decarboxylation of silyl dienol ethers with α,β-unsaturated acid fluorides. Journal of the American Chemical Society. 133: 4694-7. PMID 21391673 DOI: 10.1021/Ja111067J |
0.438 |
|
| 2011 |
Hierold J, Hsia T, Lupton DW. The Grob/Eschenmoser fragmentation of cycloalkanones bearing β-electron withdrawing groups: a general strategy to acyclic synthetic intermediates Organic and Biomolecular Chemistry. 9: 783-792. PMID 21103511 DOI: 10.1039/C0Ob00632G |
0.428 |
|
| 2011 |
Ryan SJ, Candish L, Martínez I, Lupton DW. Enabling the development of N-Heterocyclic Carbene (NHC) catalyzed reactions: Practical methods for the preparation of 1-acyl-2-alkylcycloalkenes from cycloalkanones Australian Journal of Chemistry. 64: 1148-1157. DOI: 10.1071/Ch11183 |
0.443 |
|
| 2011 |
Ryan S, Candish L, Lupton DW. N-heterocyclic carbene (NHC)-catalyzed all-carbon [4+2] cycloaddition-decarboxylation Synlett. 2011: 2275-2278. DOI: 10.1055/S-0030-1261226 |
0.347 |
|
| 2011 |
Pandiancherri S, Lupton DW. Preparation of 2-azaallyl anions and imines from N-chloroamines and their cycloaddition and allylation Tetrahedron Letters. 52: 671-674. DOI: 10.1016/J.Tetlet.2010.11.142 |
0.443 |
|
| 2011 |
Gee WJ, Hierold J, MacLellan JG, Andrews PC, Lupton DW, Junk PC. Chiral lanthanoid dimers ligated by carbohydrate-based diketonates: Catalytic and luminescent properties European Journal of Inorganic Chemistry. 3755-3760. DOI: 10.1002/Ejic.201100505 |
0.373 |
|
| 2010 |
Candish L, Lupton DW. The total synthesis of (-)-7-deoxyloganin via N-heterocyclic carbene catalyzed rearrangement of α,β-unsaturated enol esters. Organic Letters. 12: 4836-4839. PMID 20873828 DOI: 10.1021/Ol101983H |
0.4 |
|
| 2010 |
Hierold J, Gray-Weale A, Lupton DW. A divergent synthesis of modular dendrimers via sequential C–C bond fragmentation thio-Michael addition Chemical Communications. 46: 6789-6791. PMID 20730163 DOI: 10.1039/C0Cc02289F |
0.464 |
|
| 2010 |
Ngatimin M, Lupton DW. The Discovery of Catalytic Enantioselective Polyvalent Iodine Mediated Reactions Australian Journal of Chemistry. 63: 653-658. DOI: 10.1071/Ch09625 |
0.425 |
|
| 2010 |
Banwell MG, Jones MT, Loong DTJ, Lupton DW, Pinkerton DM, Ray JK, Willis AC. A Pd[0]-catalyzed Ullmann cross-coupling/reductive cyclization approach to C-3 mono-alkylated oxindoles and related compounds Tetrahedron. 66: 9252-9262. DOI: 10.1016/J.Tet.2010.09.042 |
0.535 |
|
| 2009 |
Ryan SJ, Candish L, Lupton DW. N-heterocyclic carbene-catalyzed generation of alpha,beta-unsaturated acyl imidazoliums: synthesis of dihydropyranones by their reaction with enolates. Journal of the American Chemical Society. 131: 14176-7. PMID 19757788 DOI: 10.1021/Ja905501Z |
0.359 |
|
| 2009 |
Ryan SJ, Thompson CD, Lupton DW. A Synthetic and Computational Investigation into the Direct Synthesis of α -Hydroxymethylated Enones from β-keto Phosphonates Australian Journal of Chemistry. 62: 720-727. DOI: 10.1071/Ch09301 |
0.45 |
|
| 2009 |
Ngatimin M, Gartshore CJ, Kindler JP, Naidu S, Lupton DW. The α-halogenation of α,β-unsaturated carbonyls and dihalogenation of alkenes using bisacetoxyiodobenzene/pyridine hydrohalides Tetrahedron Letters. 50: 6008-6011. DOI: 10.1016/J.Tetlet.2009.08.038 |
0.38 |
|
| 2008 |
Harvey MJ, Banwell MG, Lupton DW. The synthesis of compounds related to the indole-indoline core of the vinca alkaloids (+)-vinblastine and (+)-vincristine Tetrahedron Letters. 49: 4780-4783. DOI: 10.1016/J.Tetlet.2008.05.082 |
0.53 |
|
| 2007 |
Trost BM, Lupton DW. Dinuclear zinc-catalyzed enantioselective Aza-Henry reaction. Organic Letters. 9: 2023-6. PMID 17439228 DOI: 10.1021/Ol070618E |
0.511 |
|
| 2005 |
Banwell MG, Lupton DW. Exploiting the palladium[0]-catalysed Ullmann cross-coupling reaction in natural products chemistry: application to a total synthesis of the alkaloid (+/-)-aspidospermidine. Organic & Biomolecular Chemistry. 3: 213-5. PMID 15632959 DOI: 10.1039/B415977B |
0.567 |
|
| 2005 |
Banwell MG, Lupton DW, Willis AC. Application of the palladium(0)-catalyzed ullmann cross-coupling reaction in a total synthesis of (±)-aspidospermidine and thus representing an approach to the lower hemisphere of the binary indole-indoline alkaloid vinblastine Australian Journal of Chemistry. 58: 722-737. DOI: 10.1071/Ch05181 |
0.598 |
|
| 2005 |
Banwell MG, Edwards AJ, Lupton DW, Whited G. Whole-Cell Biotransformation of m-Ethyltoluene into 1S,6R-5-Ethyl-1,6-dihydroxycyclohexa-2,4-diene-1-carboxylic Acid as an Approach to the C-Ring of the Binary Indole - Indoline Alkaloid Vinblastine Australian Journal of Chemistry. 58: 14. DOI: 10.1071/Ch04185 |
0.482 |
|
| 2004 |
Banwell MG, Lupton DW, Ma X, Renner J, Sydnes MO. Synthesis of quinolines, 2-quinolones, phenanthridines, and 6(5h)-phenanthridinones via palladium[0]-mediated Ullmann cross-coupling of 1-bromo-2-nitroarenes with beta-halo-enals, -enones, or -esters. Organic Letters. 6: 2741-4. PMID 15281758 DOI: 10.1021/Ol0490375 |
0.558 |
|
| 2003 |
Banwell MG, Kelly BD, Kokas OJ, Lupton DW. Synthesis of indoles via palladium[0]-mediated Ullmann cross-coupling of o-halonitroarenes with alpha-halo-enones or -enals. Organic Letters. 5: 2497-500. PMID 12841764 DOI: 10.1021/Ol034745W |
0.508 |
|
| 2002 |
Avery TD, Jenkins NF, Kimber MC, Lupton DW, Taylor DK. First examples of the catalytic asymmetric ring-opening of meso 1,2-dioxines utilising cobalt(II) complexes with optically active tetradentate Schiff base ligands: Formation of enantio-enriched cyclopropanes Chemical Communications. 1: 28-29. PMID 12120294 DOI: 10.1039/B109187P |
0.381 |
|
| 2002 |
Lupton DW, Taylor DK. New mechanistic aspects on the catalytic transformation of vinylthiiranes to mono and disubstituted 3,6-dihydro-1,2-dithiins by tungsten pentacarbonyl monoacetonitrile Tetrahedron. 58: 4517-4527. DOI: 10.1016/S0040-4020(02)00398-8 |
0.413 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2023 |
Cao J, Seitz A, Forni JA, Polyzos A, Lupton DW. Radical coupling initiated by organophosphine addition to ynoates. Angewandte Chemie (International Ed. in English). e202303869. PMID 37188643 DOI: 10.1002/anie.202303869 |
0.297 |
|
| 2013 |
Lupton DW. Synthcon2: a forum for Australian organic chemists Australian Journal of Chemistry. 66: 843-843. DOI: 10.1071/Ch13396 |
0.293 |
|
| 2010 |
Gartshore CJ, Lupton DW. Readily Accessible Oxazolidine Nitroxyl Radicals: Bifunctional Cocatalysts for Simplified Copper Based Aerobic Oxidation Advanced Synthesis & Catalysis. 352: 3321-3328. DOI: 10.1002/Adsc.201000627 |
0.287 |
|
| 2013 |
Gass IA, Tewary S, Nafady A, Chilton NF, Gartshore CJ, Asadi M, Lupton DW, Moubaraki B, Bond AM, Boas JF, Guo SX, Rajaraman G, Murray KS. Observation of ferromagnetic exchange, spin crossover, reductively induced oxidation, and field-induced slow magnetic relaxation in monomeric cobalt nitroxides. Inorganic Chemistry. 52: 7557-72. PMID 23777336 DOI: 10.1021/Ic400565H |
0.27 |
|
| 2015 |
Kröger S, Wong YF, Chin ST, Grant J, Lupton D, Marriott PJ. Evaluation of reversible interconversion in comprehensive two-dimensional gas chromatography using enantioselective columns in first and second dimensions. Journal of Chromatography. A. 1404: 104-14. PMID 26058951 DOI: 10.1016/J.Chroma.2015.05.049 |
0.27 |
|
| 2011 |
Gass IA, Gartshore CJ, Lupton DW, Moubaraki B, Nafady A, Bond AM, Boas JF, Cashion JD, Milsmann C, Wieghardt K, Murray KS. Anion dependent redox changes in iron bis-terdentate nitroxide {NNO} chelates. Inorganic Chemistry. 50: 3052-64. PMID 21384832 DOI: 10.1021/Ic102588H |
0.267 |
|
| 2014 |
Gass IA, Asadi M, Lupton DW, Moubaraki B, Bond AM, Guo SX, Murray KS. Manganese(II) oxazolidine nitroxide chelates: Structure, magnetism, and redox properties Australian Journal of Chemistry. 67: 1618-1624. DOI: 10.1071/Ch14390 |
0.257 |
|
| 2015 |
Bonke SA, Wiechen M, Hocking RK, Fang XY, Lupton DW, MacFarlane DR, Spiccia L. Electrosynthesis of highly transparent cobalt oxide water oxidation catalyst films from cobalt aminopolycarboxylate complexes. Chemsuschem. 8: 1394-403. PMID 25826458 DOI: 10.1002/Cssc.201403188 |
0.257 |
|
| 2014 |
Gass IA, Tewary S, Rajaraman G, Asadi M, Lupton DW, Moubaraki B, Chastanet G, Létard JF, Murray KS. Solvate-dependent spin crossover and exchange in cobalt(II) oxazolidine nitroxide chelates. Inorganic Chemistry. 53: 5055-66. PMID 24805925 DOI: 10.1021/Ic5001057 |
0.252 |
|
| 2018 |
Gass IA, Lu J, Asadi M, Lupton DW, Forsyth CM, Geoghegan BL, Moubaraki B, Cashion JD, Martin LL, Bond AM, Murray KS. Use of the TCNQF Dianion in the Spontaneous Redox Formation of [Fe (L ) ][TCNQF ]. Chempluschem. 83: 658-668. PMID 31950640 DOI: 10.1002/Cplu.201800010 |
0.234 |
|
| 2017 |
Pedersen AH, Geoghegan BL, Nichol GS, Lupton DW, Murray KS, Martínez-Lillo J, Gass IA, Brechin EK. Hexahalorhenate(iv) salts of metal oxazolidine nitroxides. Dalton Transactions (Cambridge, England : 2003). PMID 28374882 DOI: 10.1039/C7Dt00752C |
0.218 |
|
| 2019 |
Belousoff MJ, Venugopal H, Wright A, Senoner S, Stuart I, Stubenrauch C, Bamert RS, Lupton DW, Lithgow T. CryoEM guided development of antibiotics for drug-resistant bacteria. Chemmedchem. PMID 30667174 DOI: 10.1002/Cmdc.201900042 |
0.215 |
|
| 2024 |
Breeze CW, Nakano Y, Campbell EC, Frkic RL, Lupton DW, Jackson CJ. Mononuclear binding and catalytic activity of europium(III) and gadolinium(III) at the active site of the model metalloenzyme phosphotriesterase. Acta Crystallographica. Section D, Structural Biology. 80: 289-298. PMID 38512071 DOI: 10.1107/S2059798324002316 |
0.188 |
|
| 2022 |
Kang SW, Antoney J, Frkic RL, Lupton DW, Speight R, Scott C, Jackson CJ. Asymmetric Ene-Reduction of α,β-Unsaturated Compounds by F-Dependent Oxidoreductases A Enzymes from . Biochemistry. PMID 36637210 DOI: 10.1021/acs.biochem.2c00557 |
0.18 |
|
| 2017 |
Lupton D, Belousoff MJ. The redesign of oxazolidinone antibiotics in response to Staphylococcus aureus. Future Microbiology. 12: 1113-1117. PMID 28876083 DOI: 10.2217/Fmb-2017-0126 |
0.172 |
|
| 2022 |
Vujcic B, Wyllie J, Burns J, White KF, Cromwell S, Lupton DW, Dutton J, Soares da Costa TP, Houston SD. Cage Hydrocarbons as Linkers in Dimeric Drug Design: Case Studies with Trimethoprim and Tedizolid. Bioorganic & Medicinal Chemistry Letters. 129086. PMID 36423825 DOI: 10.1016/j.bmcl.2022.129086 |
0.143 |
|
| 2023 |
Kang SW, Antoney J, Lupton D, Speight R, Scott C, Jackson CJ. Asymmetric ene-reduction by F420-dependent oxidoreductases B (FDOR-B) enzymes from Mycobacterium smegmatis. Chembiochem : a European Journal of Chemical Biology. PMID 36716144 DOI: 10.1002/cbic.202200797 |
0.138 |
|
| 2023 |
Nakano Y, Lupton DW. One carbon-four new bonds. Science (New York, N.Y.). 379: 439-440. PMID 36730389 DOI: 10.1126/science.adf2201 |
0.134 |
|
| 2022 |
Hashad RA, Jap E, Casey JL, Ho YTC, Wright A, Thalmann C, Sleeman M, Lupton DW, Hagemeyer CE, Cryle MJ, Robert R, Alt K. Chemoselective methionine labelling of recombinant Trastuzumab shows high in vitro and in vivo tumour targeting. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 36451579 DOI: 10.1002/chem.202202491 |
0.132 |
|
| 2020 |
Wright A, Deane-Alder K, Marschall E, Bamert R, Venugopal H, Lithgow T, Lupton DW, Belousoff MJ. Characterization of the Core Ribosomal Binding Region for the Oxazolidone Family of Antibiotics Using Cryo-EM. Acs Pharmacology & Translational Science. 3: 425-432. PMID 32566908 DOI: 10.1021/acsptsci.0c00041 |
0.089 |
|
| 2022 |
Perlaza-Jiménez L, Tan KS, Piper SJ, Johnson RM, Bamert RS, Stubenrauch CJ, Wright A, Lupton D, Lithgow T, Belousoff MJ. A Structurally Characterized Evolutionary Escape Route from Treatment with the Antibiotic Linezolid. Microbiology Spectrum. e0058322. PMID 35736238 DOI: 10.1128/spectrum.00583-22 |
0.049 |
|
| 2015 |
Kamour A, George N, Gwynnette D, Cooper G, Lupton D, Eddleston M, Thompson JP, Vale JA, Thanacoody HK, Hill S, Thomas SH. Increasing frequency of severe clinical toxicity after use of 2,4-dinitrophenol in the UK: a report from the National Poisons Information Service. Emergency Medicine Journal : Emj. 32: 383-6. PMID 24957806 DOI: 10.1136/emermed-2013-203335 |
0.038 |
|
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