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 |
|
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