| Year |
Citation |
Score |
| 2024 |
Clark KF, Tyerman S, Evans L, Robertson CM, Murphy JA. An assay for aryl radicals using BHAS coupling. Organic & Biomolecular Chemistry. PMID 38197449 DOI: 10.1039/d3ob01743e |
0.379 |
|
| 2023 |
Clark KF, Tyerman S, Evans L, Robertson CM, Nelson DJ, Kennedy AR, Murphy JA. A Hierarchy of Ligands Controls Formation and Reaction of Aryl Radicals in Pd-Catalyzed Ground-State Base-Promoted Coupling Reactions. Journal of the American Chemical Society. PMID 37713365 DOI: 10.1021/jacs.3c05470 |
0.325 |
|
| 2022 |
Bell JD, Robb I, Murphy JA. Highly selective α-aryloxyalkyl C-H functionalisation of aryl alkyl ethers. Chemical Science. 13: 12921-12926. PMID 36519054 DOI: 10.1039/d2sc04463c |
0.387 |
|
| 2022 |
Pratley C, Fenner S, Murphy JA. Nitrogen-Centered Radicals in Functionalization of sp Systems: Generation, Reactivity, and Applications in Synthesis. Chemical Reviews. PMID 35285636 DOI: 10.1021/acs.chemrev.1c00831 |
0.325 |
|
| 2021 |
Kolodziejczak K, Stewart AJ, Tuttle T, Murphy JA. Radical and Ionic Mechanisms in Rearrangements of -Tolyl Aryl Ethers and Amines Initiated by the Grubbs-Stoltz Reagent, EtSiH/KOBu. Molecules (Basel, Switzerland). 26. PMID 34833971 DOI: 10.3390/molecules26226879 |
0.393 |
|
| 2020 |
Smith AJ, Dimitrova D, Arokianathar JN, Clark KF, Poole DL, Leach SG, Murphy JA. EtSiH + KO Bu provide multiple reactive intermediates that compete in the reactions and rearrangements of benzylnitriles and indolenines. Chemical Science. 11: 12364-12370. PMID 34094446 DOI: 10.1039/d0sc04244g |
0.372 |
|
| 2020 |
Smith AJ, Dimitrova D, Arokianathar JN, Kolodziejczak K, Young A, Allison M, Poole DL, Leach SG, Parkinson JA, Tuttle T, Murphy JA. New reductive rearrangement of -arylindoles triggered by the Grubbs-Stoltz reagent EtSiH/KO Bu. Chemical Science. 11: 3719-3726. PMID 34094060 DOI: 10.1039/d0sc00361a |
0.321 |
|
| 2020 |
Lawson CA, Dominey AP, Williams GD, Murphy JA. Visible light-mediated Smiles rearrangements and annulations of non-activated aromatics. Chemical Communications (Cambridge, England). PMID 32852011 DOI: 10.1039/D0Cc04666C |
0.371 |
|
| 2020 |
Rohrbach S, Murphy JA, Tuttle T. Computational Study on the Boundary Between the Concerted and Stepwise Mechanism of Bimolecular SNAr Reactions. Journal of the American Chemical Society. PMID 32786763 DOI: 10.1021/Jacs.0C01975 |
0.419 |
|
| 2020 |
Lippa RA, Murphy JA, Barrett TN. Facile synthesis of 7-alkyl-1,2,3,4-tetrahydro-1,8-naphthyridines as arginine mimetics using a Horner-Wadsworth-Emmons-based approach. Beilstein Journal of Organic Chemistry. 16: 1617-1626. PMID 32704328 DOI: 10.3762/Bjoc.16.134 |
0.317 |
|
| 2020 |
Murphy J, Turner O, Hirst D. Hydrogen Atom Transfer-Mediated Domino Cyclisation Reaction to Access (Spiro)Quinazolinones. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31922300 DOI: 10.1002/Chem.201905712 |
0.421 |
|
| 2020 |
Arokianathar JN, Kolodziejczak K, Bugden FE, Clark KF, Tuttle T, Murphy JA. Benzylic C−H Functionalisation by [Et
3
SiH+KO
t
Bu] leads to Radical Rearrangements in
o‐
tolyl Aryl Ethers, Amines and Sulfides Advanced Synthesis & Catalysis. 362: 2260-2267. DOI: 10.1002/Adsc.202000356 |
0.466 |
|
| 2019 |
Rohrbach S, Shah RS, Tuttle T, Murphy JA. Corrigendum: Neutral Organic Super Electron Donors Made Catalytic. Angewandte Chemie (International Ed. in English). 58: 15183. PMID 31609546 DOI: 10.1002/Anie.201910425 |
0.362 |
|
| 2019 |
Murphy J, Rohrbach S, Shah RS, Tuttle T. CatalySED! Neutral Organic Super Electron Donors Made Catalytic. Angewandte Chemie (International Ed. in English). PMID 31222953 DOI: 10.1002/Anie.201905814 |
0.456 |
|
| 2019 |
Murphy J, Rohrbach S, Smith AJ, Pang JH, Poole DL, Tuttle T, Chiba S. Concerted Nucleophilic Aromatic Substitution Reactions. Angewandte Chemie (International Ed. in English). PMID 30990931 DOI: 10.1002/Anie.201902216 |
0.449 |
|
| 2019 |
Nocera G, Murphy JA. Ground State Cross-Coupling of Haloarenes with Arenes Initiated by Organic Electron Donors, Formed in situ: An Overview Synthesis. 52: 327-336. DOI: 10.1055/S-0039-1690614 |
0.459 |
|
| 2019 |
Smith AJ, Poole DL, Murphy JA. The role of organic electron donors in the initiation of BHAS base-induced coupling reactions between haloarenes and arenes Science China Chemistry. 62: 1425-1438. DOI: 10.1007/S11426-019-9611-X |
0.475 |
|
| 2019 |
Palumbo F, Rohrbach S, Tuttle T, Murphy JA. N‐Silylation of Amines Mediated by Et
3
SiH/KO
t
Bu Helvetica Chimica Acta. 102. DOI: 10.1002/Hlca.201900235 |
0.412 |
|
| 2019 |
Rohrbach S, Shah RS, Tuttle T, Murphy JA. Berichtigung: Neutral Organic Super Electron Donors Made Catalytic Angewandte Chemie. 131: 15325-15325. DOI: 10.1002/Ange.201910425 |
0.362 |
|
| 2018 |
Murphy J, Turner O, Hirst D, Talbot E. Hydrogen Atom Transfer-Mediated Cyclisations of Nitriles. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30341926 DOI: 10.1002/Chem.201805236 |
0.42 |
|
| 2018 |
Bogdos MK, Pinard E, Murphy JA. Applications of organocatalysed visible-light photoredox reactions for medicinal chemistry. Beilstein Journal of Organic Chemistry. 14: 2035-2064. PMID 30202458 DOI: 10.3762/Bjoc.14.179 |
0.356 |
|
| 2018 |
Barham JP, Dalton SE, Allison M, Nocera G, Young A, John MP, McGuire TM, Campos S, Tuttle T, Murphy JA. Dual Roles for Potassium Hydride in Haloarene Reduction: CSAr and SET Reduction via Organic Electron Donors Formed in Benzene. Journal of the American Chemical Society. PMID 30119605 DOI: 10.1021/Jacs.8B07632 |
0.763 |
|
| 2018 |
Nocera G, Young A, Palumbo F, Emery KJ, Coulthard G, McGuire TM, Tuttle T, Murphy JA. Electron Transfer Reactions: KOtBu (but not NaOtBu) Photo-reduces Benzophenone, under Activation by Visible Light. Journal of the American Chemical Society. PMID 29996048 DOI: 10.1021/Jacs.8B06089 |
0.465 |
|
| 2018 |
Emery KJ, Young A, Arokianathar JN, Tuttle T, Murphy JA. KOBu as a Single Electron Donor? Revisiting the Halogenation of Alkanes with CBr₄ and CCl₄. Molecules (Basel, Switzerland). 23. PMID 29724009 DOI: 10.3390/Molecules23051055 |
0.454 |
|
| 2018 |
Cumine F, Palumbo F, Murphy JA. Reduction of nitroarenes, azoarenes and hydrazine derivatives by an organic super electron donor Tetrahedron. 74: 5539-5545. DOI: 10.1016/J.Tet.2018.04.069 |
0.42 |
|
| 2017 |
Emery KJ, Tuttle T, Murphy JA. Evidence of single electron transfer from the enolate anion of an N,N'-dialkyldiketopiperazine additive in BHAS coupling reactions. Organic & Biomolecular Chemistry. PMID 29022630 DOI: 10.1039/C7Ob02209C |
0.441 |
|
| 2017 |
Murphy J, Smith A, Young A, Rohrbach S, O'Connor E, Allison M, Wang HS, Poole D, Tuttle T. Electron Transfer and Hydride Transfer Pathways in the Stoltz-Grubbs Reducing System (KOtBu-Et3SiH). Angewandte Chemie (International Ed. in English). PMID 28892585 DOI: 10.1002/Anie.201707914 |
0.477 |
|
| 2017 |
Cumine F, Zhou S, Tuttle T, Murphy JA. A study of diketopiperazines as electron-donor initiators in transition metal-free haloarene-arene coupling. Organic & Biomolecular Chemistry. PMID 28362016 DOI: 10.1039/C7Ob00036G |
0.347 |
|
| 2017 |
Emery KJ, Murphy JA, Tuttle T. Effect of solvent on radical cyclisation pathways: SRN1 vs. aryl-aryl bond forming mechanisms. Organic & Biomolecular Chemistry. PMID 28050609 DOI: 10.1039/C6Ob02684B |
0.503 |
|
| 2017 |
Cumine F, Young A, Reissig H, Tuttle T, Murphy JA. A Computational Study of Anionic Alkoxide-Allene and Amide-Allene Cyclizations European Journal of Organic Chemistry. 2017: 6867-6871. DOI: 10.1002/Ejoc.201701381 |
0.431 |
|
| 2016 |
Barham JP, John MP, Murphy JA. Contra-Thermodynamic Hydrogen Atom Abstraction in the Selective C-H Functionalisation of Trialkylamine N-CH3 Groups. Journal of the American Chemical Society. PMID 27809514 DOI: 10.1021/Jacs.6B09690 |
0.7 |
|
| 2016 |
Barham JP, Coulthard G, Emery KJ, Doni E, Cumine F, Nocera G, John MP, Berlouis LE, McGuire TM, Tuttle T, Murphy JA. KOtBu: a Privileged Reagent for Electron Transfer Reactions? Journal of the American Chemical Society. PMID 27183183 DOI: 10.1021/Jacs.6B03282 |
0.753 |
|
| 2016 |
Barham JP, Coulthard G, Kane RG, Delgado N, John MP, Murphy JA. Double Deprotonation of Pyridinols Generates Potent Organic Electron-Donor Initiators for Haloarene-Arene Coupling. Angewandte Chemie (International Ed. in English). PMID 26938924 DOI: 10.1002/Anie.201511847 |
0.755 |
|
| 2016 |
Anderson GM, Cameron I, Murphy JA, Tuttle T. Predicting the reducing power of organic super electron donors Rsc Advances. 6: 11335-11343. DOI: 10.1039/C5Ra26483A |
0.396 |
|
| 2016 |
Emery KJ, Tuttle T, Kennedy AR, Murphy JA. C–C bond-forming reactions of ground-state aryl halides under reductive activation Tetrahedron. 72: 7875-7887. DOI: 10.1016/J.Tet.2016.05.083 |
0.442 |
|
| 2016 |
Massey RS, Quinn P, Zhou S, Murphy JA, O'Donoghue AC. Proton transfer reactions of a bridged bis-propyl bis-imidazolium salt Journal of Physical Organic Chemistry. DOI: 10.1002/Poc.3567 |
0.424 |
|
| 2015 |
Hanson SS, Doni E, Traboulsee KT, Coulthard G, Murphy JA, Dyker CA. Pushing the Limits of Neutral Organic Electron Donors: A Tetra(iminophosphorano)-Substituted Bispyridinylidene. Angewandte Chemie (International Ed. in English). 54: 11236-9. PMID 26213345 DOI: 10.1002/Anie.201505378 |
0.441 |
|
| 2015 |
Doni E, Zhou S, Murphy JA. Electron transfer-induced coupling of haloarenes to styrenes and 1,1-diphenylethenes triggered by diketopiperazines and Potassium tert-butoxide. Molecules (Basel, Switzerland). 20: 1755-74. PMID 25621421 DOI: 10.3390/Molecules20021755 |
0.441 |
|
| 2014 |
Barham JP, John MP, Murphy JA. One-pot functionalisation of N-substituted tetrahydroisoquinolines by photooxidation and tunable organometallic trapping of iminium intermediates. Beilstein Journal of Organic Chemistry. 10: 2981-8. PMID 25550765 DOI: 10.3762/Bjoc.10.316 |
0.732 |
|
| 2014 |
Zhou S, Doni E, Anderson GM, Kane RG, MacDougall SW, Ironmonger VM, Tuttle T, Murphy JA. Identifying the roles of amino acids, alcohols and 1,2-diamines as mediators in coupling of haloarenes to arenes. Journal of the American Chemical Society. 136: 17818-26. PMID 25474411 DOI: 10.1021/Ja5101036 |
0.378 |
|
| 2014 |
Doni E, Murphy JA. Evolution of neutral organic super-electron-donors and their applications. Chemical Communications (Cambridge, England). 50: 6073-87. PMID 24690952 DOI: 10.1039/C3Cc48969H |
0.413 |
|
| 2014 |
Murphy JA. Discovery and development of organic super-electron-donors. The Journal of Organic Chemistry. 79: 3731-46. PMID 24605904 DOI: 10.1021/Jo500071U |
0.471 |
|
| 2014 |
O'Sullivan S, Doni E, Tuttle T, Murphy JA. Metal-free reductive cleavage of C-N and S-N bonds by photoactivated electron transfer from a neutral organic donor. Angewandte Chemie (International Ed. in English). 53: 474-8. PMID 24311295 DOI: 10.1002/Anie.201306543 |
0.418 |
|
| 2014 |
Doni E, Murphy JA. Reductive decyanation of malononitriles and cyanoacetates using photoactivated neutral organic super-electron-donors Organic Chemistry Frontiers. 1: 1072-1076. DOI: 10.1039/C4Qo00202D |
0.425 |
|
| 2014 |
Zhou S, Anderson GM, Mondal B, Doni E, Ironmonger V, Kranz M, Tuttle T, Murphy JA. Organic super-electron-donors: Initiators in transition metal-free haloarene-arene coupling Chemical Science. 5: 476-482. DOI: 10.1039/C3Sc52315B |
0.487 |
|
| 2013 |
Farwaha HS, Bucher G, Murphy JA. A novel neutral organic electron donor with record half-wave potential. Organic & Biomolecular Chemistry. 11: 8073-81. PMID 24150102 DOI: 10.1039/C3Ob41701H |
0.347 |
|
| 2013 |
Ueda M, Uenoyama Y, Terasoma N, Doi S, Kobayashi S, Ryu I, Murphy JA. A construction of 4,4-spirocyclic γ-lactams by tandem radical cyclization with carbon monoxide. Beilstein Journal of Organic Chemistry. 9: 1340-5. PMID 23946829 DOI: 10.3762/Bjoc.9.151 |
0.451 |
|
| 2013 |
Doni E, Mondal B, O'Sullivan S, Tuttle T, Murphy JA. Overturning established chemoselectivities: selective reduction of arenes over malonates and cyanoacetates by photoactivated organic electron donors. Journal of the American Chemical Society. 135: 10934-7. PMID 23859883 DOI: 10.1021/Ja4050168 |
0.376 |
|
| 2013 |
Bochatay VN, Boissarie PJ, Murphy JA, Suckling CJ, Lang S. Mechanistic exploration of the palladium-catalyzed process for the synthesis of benzoxazoles and benzothiazoles. The Journal of Organic Chemistry. 78: 1471-7. PMID 23316812 DOI: 10.1021/Jo302544D |
0.375 |
|
| 2013 |
Doni E, O'Sullivan S, Murphy JA. Metal-free reductive cleavage of benzylic esters and ethers: fragmentations result from single and double electron transfers. Angewandte Chemie (International Ed. in English). 52: 2239-42. PMID 23315943 DOI: 10.1002/Anie.201208066 |
0.458 |
|
| 2013 |
Sword R, O'Sullivan S, Murphy JA. A novel organic electron donor derived from N-methylisatin Australian Journal of Chemistry. 66: 314-322. DOI: 10.1071/Ch12480 |
0.419 |
|
| 2012 |
Garnier J, Thomson DW, Zhou S, Jolly PI, Berlouis LE, Murphy JA. Hybrid super electron donors - preparation and reactivity. Beilstein Journal of Organic Chemistry. 8: 994-1002. PMID 23019427 DOI: 10.3762/Bjoc.8.112 |
0.461 |
|
| 2012 |
Zhou S, Farwaha H, Murphy JA. The development of organic super electron donors. Chimia. 66: 418-24. PMID 22871286 DOI: 10.2533/Chimia.2012.418 |
0.332 |
|
| 2012 |
Kovacevic LS, Idziak C, Markevicius A, Scullion C, Corr MJ, Kennedy AR, Tuttle T, Murphy JA. Superelectrophilic amidine dications: dealkylation by triflate anion. Angewandte Chemie (International Ed. in English). 51: 8516-9. PMID 22807275 DOI: 10.1002/Anie.201202990 |
0.358 |
|
| 2012 |
Jolly PI, Fleary-Roberts N, O'Sullivan S, Doni E, Zhou S, Murphy JA. Reactions of triflate esters and triflamides with an organic neutral super-electron-donor. Organic & Biomolecular Chemistry. 10: 5807-10. PMID 22395414 DOI: 10.1039/C2Ob25116G |
0.445 |
|
| 2012 |
Cahard E, Schoenebeck F, Garnier J, Cutulic SP, Zhou S, Murphy JA. Electron transfer to benzenes by photoactivated neutral organic electron donor molecules. Angewandte Chemie (International Ed. in English). 51: 3673-6. PMID 22389276 DOI: 10.1002/Anie.201200084 |
0.641 |
|
| 2012 |
Jolly PI, Zhou S, Thomson DW, Garnier J, Parkinson JA, Tuttle T, Murphy JA. Imidazole-derived carbenes and their elusive tetraazafulvalene dimers Chemical Science. 3: 1675-1679. DOI: 10.1039/C2Sc20054F |
0.433 |
|
| 2011 |
Boissarie PJ, Hamilton ZE, Lang S, Murphy JA, Suckling CJ. A powerful palladium-catalyzed multicomponent process for the preparation of oxazolines and benzoxazoles. Organic Letters. 13: 6256-9. PMID 22047037 DOI: 10.1021/Ol202725Y |
0.33 |
|
| 2011 |
Sword R, Baldwin LA, Murphy JA. Fragmentations observed in the reactions of α-methoxy-γ-alkoxyalkyl iodide substrates with super-electron-donors derived from 4-DMAP and N-methylbenzimidazole. Organic & Biomolecular Chemistry. 9: 3560-70. PMID 21445392 DOI: 10.1039/C0Ob01282C |
0.483 |
|
| 2010 |
Murphy JA. Physical organic chemistry. Beilstein Journal of Organic Chemistry. 6: 1025. PMID 21085500 DOI: 10.3762/Bjoc.6.116 |
0.373 |
|
| 2010 |
Findlay NJ, Park SR, Schoenebeck F, Cahard E, Zhou SZ, Berlouis LE, Spicer MD, Tuttle T, Murphy JA. Reductions of challenging organic substrates by a nickel complex of a noninnocent crown carbene ligand. Journal of the American Chemical Society. 132: 15462-4. PMID 20961105 DOI: 10.1021/Ja107703N |
0.576 |
|
| 2010 |
Garnier J, Kennedy AR, Berlouis LE, Turner AT, Murphy JA. Structure and reactivity in neutral organic electron donors derived from 4-dimethylaminopyridine. Beilstein Journal of Organic Chemistry. 6. PMID 20703372 DOI: 10.3762/Bjoc.6.73 |
0.397 |
|
| 2010 |
Murphy J, Macleod F, Lang S. The 2-(2-Azidoethyl)cycloalkanone Strategy for Bridged Amides and Medium-Sized Cyclic Amine Derivatives in the Aubé-Schmidt Reaction Synlett. 2010: 529-534. DOI: 10.1055/S-0029-1219340 |
0.456 |
|
| 2010 |
Bashir N, Patro B, Murphy JA. ChemInform Abstract: Reactions of Arenediazonium Salts with Tetrathiafulvalene and Related Electron Donors: A Study of “Radical-Polar Crossover” Reactions Cheminform. 32: no-no. DOI: 10.1002/chin.200122278 |
0.336 |
|
| 2010 |
Gonzalez Martin C, Murphy JA, Smith CR. ChemInform Abstract: Replacing Tin in Radical Chemistry: N-Ethylpiperidine Hypophosphite in Cyclization Reactions of Aryl Radicals. Cheminform. 31: no-no. DOI: 10.1002/chin.200023046 |
0.387 |
|
| 2010 |
Kizil M, Patro B, Callaghan O, Murphy JA, Hursthouse MB, Hibbs D. ChemInform Abstract: Tandem Radical Cyclizations on Iodoaryl Azides: Synthesis of the Core Tetracycle of Aspidosperma Alkaloids. Cheminform. 31: no-no. DOI: 10.1002/chin.200005246 |
0.319 |
|
| 2010 |
MURPHY JA, RASHEED F, ROOME SJ, SCOTT KA, LEWIS N. ChemInform Abstract: Intramolecular Termination of Radical-Polar Crossover Reactions. Cheminform. 29: no-no. DOI: 10.1002/chin.199849061 |
0.313 |
|
| 2010 |
KIZIL M, MURPHY JA. ChemInform Abstract: A New Free Radical Route to Oximes Using Alkyl Halides, Hexabutylditin and Readily Available Nitrite Esters. Cheminform. 29: no-no. DOI: 10.1002/chin.199811104 |
0.317 |
|
| 2010 |
FLETCHER RJ, HIBBS DE, HURSTHOUSE M, LAMPARD C, MURPHY JA, ROOME SJ. ChemInform Abstract: Stereocontrolled Synthesis of Complex Polycycles Using Tetrathiafulvalene Mediated Radical-Polar Crossover Reactions. Cheminform. 27: no-no. DOI: 10.1002/chin.199635051 |
0.326 |
|
| 2010 |
MURPHY JA, RASHEED F, ROOME SJ, LEWIS N. ChemInform Abstract: Termination of Radical-Polar Crossover Reactions by Intramolecular Nucleophiles. Cheminform. 27: no-no. DOI: 10.1002/chin.199635050 |
0.326 |
|
| 2010 |
KIZIL M, LAMPARD C, MURPHY JA. ChemInform Abstract: Studies of the Tetrathiafulvalene Mediated Radical-Polar Crossover Reaction Directed Toward the Total Synthesis of Alkaloid Natural Products. Cheminform. 27: no-no. DOI: 10.1002/chin.199632261 |
0.316 |
|
| 2010 |
BATSANOV AS, BEGLEY MJ, FLETCHER RJ, MURPHY JA, SHERBURN MS. ChemInform Abstract: Stereocontrol in Cyclization of Dioxolanyl Radicals. Cheminform. 26: no-no. DOI: 10.1002/chin.199537047 |
0.319 |
|
| 2010 |
GRIFFITHS J, MURPHY JA. ChemInform Abstract: Reaction Mechanisms. Part 3. Free-Radical Reactions Cheminform. 25: no-no. DOI: 10.1002/chin.199409305 |
0.331 |
|
| 2010 |
MURPHY JA, SHERBURN MS. ChemInform Abstract: Reaction Mechanisms. Part 3. Free Radicals Cheminform. 23: no-no. DOI: 10.1002/chin.199216335 |
0.334 |
|
| 2010 |
MURPHY JA, SHERBURN MS. ChemInform Abstract: Intramolecular Free-Radical Substitution of Pyridinium Rings. Cheminform. 22: no-no. DOI: 10.1002/chin.199135168 |
0.314 |
|
| 2009 |
Corr MJ, Roydhouse MD, Gibson KF, Zhou SZ, Kennedy AR, Murphy JA. Amidine dications as superelectrophiles. Journal of the American Chemical Society. 131: 17980-5. PMID 19916499 DOI: 10.1021/Ja908191K |
0.39 |
|
| 2009 |
Cutulic SP, Findlay NJ, Zhou SZ, Chrystal EJ, Murphy JA. Metal-free reductive cleavage of C-O sigma-bonds in acyloin derivatives by an organic neutral super-electron-donor. The Journal of Organic Chemistry. 74: 8713-8. PMID 19845372 DOI: 10.1021/Jo901815T |
0.417 |
|
| 2009 |
Corr MJ, Gibson KF, Kennedy AR, Murphy JA. Amidine dications: isolation and [Fe]-hydrogenase-related hydrogenation. Journal of the American Chemical Society. 131: 9174-5. PMID 19534467 DOI: 10.1021/Ja9035847 |
0.317 |
|
| 2009 |
Murphy JA, Schoenebeck F, Findlay NJ, Thomson DW, Zhou SZ, Garnier J. One-carbon extrusion from a tetraazafulvalene. Isolation of aldehydes and a study of their origin. Journal of the American Chemical Society. 131: 6475-9. PMID 19415936 DOI: 10.1021/Ja8092746 |
0.66 |
|
| 2009 |
Mahesh M, Murphy JA, LeStrat F, Wessel HP. Reduction of arenediazonium salts by tetrakis(dimethylamino)ethylene (TDAE): efficient formation of products derived from aryl radicals. Beilstein Journal of Organic Chemistry. 5: 1. PMID 19259337 DOI: 10.3762/Bjoc.5.1 |
0.511 |
|
| 2009 |
Hisler K, Commeureuc AG, Zhou S, Murphy JA. Synthesis of indoles via alkylidenation of acyl hydrazides Tetrahedron Letters. 50: 3290-3293. DOI: 10.1016/J.Tetlet.2009.02.060 |
0.417 |
|
| 2009 |
Park SR, Findlay NJ, Garnier J, Zhou S, Spicer MD, Murphy JA. Electron transfer activity of a cobalt crown carbene complex Tetrahedron. 65: 10756-10761. DOI: 10.1016/J.Tet.2009.10.090 |
0.353 |
|
| 2008 |
Murphy JA, Garnier J, Park SR, Schoenebeck F, Zhou SZ, Turner AT. Super-electron donors: bis-pyridinylidene formation by base treatment of pyridinium salts. Organic Letters. 10: 1227-30. PMID 18288858 DOI: 10.1021/Ol800134G |
0.643 |
|
| 2008 |
Murphy J, Garnier J, Zhou S, Turner A. One-Pot Reduction of Aryl Iodides Using 4-DMAP Methiodide Salt Synlett. 2008: 2127-2131. DOI: 10.1055/S-2008-1078242 |
0.44 |
|
| 2008 |
Murphy J, Cutulic S, Farwaha H, Zhou S, Chrystal E. Metal-Free Reductive Cleavage of N-O Bonds in Weinreb Amides by an Organic Neutral Super-Electron Donor Synlett. 2008: 2132-2136. DOI: 10.1055/S-2008-1078240 |
0.401 |
|
| 2007 |
Schoenebeck F, Murphy JA, Zhou SZ, Uenoyama Y, Miclo Y, Tuttle T. Reductive cleavage of sulfones and sulfonamides by a neutral organic super-electron-donor (S.E.D.) reagent. Journal of the American Chemical Society. 129: 13368-9. PMID 17939662 DOI: 10.1021/Ja074417H |
0.626 |
|
| 2007 |
Murphy JA, Mahesh M, McPheators G, Anand RV, McGuire TM, Carling R, Kennedy AR. Fragmentation of nitrone triflates to 9-membered rings. Organic Letters. 9: 3233-6. PMID 17650006 DOI: 10.1021/Ol071049D |
0.496 |
|
| 2007 |
Murphy JA, Zhou SZ, Thomson DW, Schoenebeck F, Mahesh M, Park SR, Tuttle T, Berlouis LE. The generation of aryl anions by double electron transfer to aryl iodides from a neutral ground-state organic super-electron donor. Angewandte Chemie (International Ed. in English). 46: 5178-83. PMID 17546715 DOI: 10.1002/Anie.200700554 |
0.66 |
|
| 2006 |
Lang S, Murphy JA. Azide rearrangements in electron-deficient systems. Chemical Society Reviews. 35: 146-56. PMID 16444296 DOI: 10.1039/B505080D |
0.441 |
|
| 2006 |
Hisler K, Tripoli R, Murphy JA. Reactions of Weinreb amides: formation of aldehydes by Wittig reactions Tetrahedron Letters. 47: 6293-6295. DOI: 10.1016/J.Tetlet.2006.06.118 |
0.433 |
|
| 2005 |
Murphy JA, Tripoli R, Khan TA, Mali UW. Novel phosphorus radical-based routes to horsfiline. Organic Letters. 7: 3287-9. PMID 16018642 DOI: 10.1021/Ol051095I |
0.407 |
|
| 2005 |
Mahesh M, Murphy JA, Wessel HP. Novel deoxygenation reaction of epoxides by indium. The Journal of Organic Chemistry. 70: 4118-23. PMID 15876104 DOI: 10.1021/Jo047904D |
0.477 |
|
| 2005 |
Murphy JA, Commeureuc AG, Snaddon TN, McGuire TM, Khan TA, Hisler K, Dewis ML, Carling R. Direct conversion of N-methoxy-N-methylamides (Weinreb amides) to ketones via a nonclassical Wittig reaction. Organic Letters. 7: 1427-9. PMID 15787523 DOI: 10.1021/Ol050337B |
0.397 |
|
| 2005 |
Murphy JA, Khan TA, Zhou SZ, Thomson DW, Mahesh M. Highly efficient reduction of unactivated aryl and alkyl iodides by a ground-state neutral organic electron donor. Angewandte Chemie (International Ed. in English). 44: 1356-60. PMID 15674987 DOI: 10.1002/Anie.200462038 |
0.443 |
|
| 2005 |
Lang S, Corr M, Muir N, Khan TA, Schoenebeck F, Murphy JA, Payne AH, Williams AC. First Organophosphorus Radical-Mediated Cyclizations to Afford Medium-Sized Rings: Eight-Membered Lactones and Seven- and Eight-Membered Lactams. Cheminform. 36. DOI: 10.1016/J.Tetlet.2005.04.032 |
0.654 |
|
| 2003 |
Lang S, Kennedy AR, Murphy JA, Payne AH. Amination of arenes through electron-deficient reaction cascades of aryl epoxyazides. Organic Letters. 5: 3655-8. PMID 14507197 DOI: 10.1021/Ol035319D |
0.481 |
|
| 2003 |
Lizos DE, Murphy JA. Concise synthesis of (+/-)-horsfiline and (+/-)-coerulescine by tandem cyclisation of iodoaryl alkenyl azides. Organic & Biomolecular Chemistry. 1: 117-22. PMID 12929397 DOI: 10.1039/B208114H |
0.367 |
|
| 2003 |
Khan TA, Tripoli R, Crawford JJ, Martin CG, Murphy JA. Diethylphosphine oxide (DEPO): high-yielding and facile preparation of indolones in water. Organic Letters. 5: 2971-4. PMID 12889921 DOI: 10.1021/Ol035173I |
0.677 |
|
| 2003 |
Commeureuc AG, Murphy JA, Dewis ML. Synthesis of muscothiazoles A and B: Critical role of methyl group substitution in RCM-based syntheses of macrocycles. Organic Letters. 5: 2785-8. PMID 12889874 DOI: 10.1021/Ol034571I |
0.335 |
|
| 2003 |
Thomson DW, Commeureuc AGJ, Berlin S, Murphy JA. Efficient route to the pineal hormone melatonin by radical-based indole synthesis Synthetic Communications. 33: 3631-3641. DOI: 10.1081/Scc-120024751 |
0.426 |
|
| 2002 |
LeStrat F, Murphy JA, Hughes M. Direct electroreductive preparation of indolines and indoles from diazonium salts. Organic Letters. 4: 2735-8. PMID 12153222 DOI: 10.1021/Ol0262643 |
0.333 |
|
| 2002 |
Zhou SZ, Bommezijn S, Murphy JA. Formal total synthesis of (+/-)-vindoline by tandem radical cyclization. Organic Letters. 4: 443-5. PMID 11820900 DOI: 10.1021/Ol0171618 |
0.397 |
|
| 2001 |
Bommezijn S, Martin CG, Kennedy AR, Lizos D, Murphy JA. 1,4-pentadienyl-3-sulfonamides: frameworks for "disfavored" radical cascade cyclizations. Organic Letters. 3: 3405-7. PMID 11594845 DOI: 10.1021/Ol0166449 |
0.44 |
|
| 2001 |
Patro B, Murphy JA. Tandem radical cyclizations with iodoaryl azides: formal total synthesis of (+/-)-aspidospermidine. Organic Letters. 2: 3599-601. PMID 11073654 DOI: 10.1021/Ol006477X |
0.416 |
|
| 2001 |
Lizos D, Tripoli R, Murphy JA. A novel and economical route to (±)-horsfiline using an aryl iodoazide tandem radical cyclisation strategy Chemical Communications. 2732-2733. DOI: 10.1039/B108622G |
0.304 |
|
| 2001 |
Patro B, Murphy JA. ChemInform Abstract: Tandem Radical Cyclizations with Iodoaryl Azides: Formal Total Synthesis of (.+-.)-Aspidospermidine. Cheminform. 32: no-no. DOI: 10.1002/chin.200111211 |
0.329 |
|
| 2000 |
Murphy JA. Free radicals in synthesis. Clean reagents affording oxidative or reductive termination Pure and Applied Chemistry. 72: 1327-1334. DOI: 10.1351/Pac200072071327 |
0.484 |
|
| 2000 |
Murphy JA, Scott KA, Sinclair RS, Martin CG, Kennedy AR, Lewis N. A radical based addition-elimination route for the preparation of indoles Journal of the Chemical Society, Perkin Transactions 1. 2395-2408. DOI: 10.1039/B002565H |
0.489 |
|
| 2000 |
Bashir N, Murphy JA. The role of neighbouring group participation in TTF-mediated ‘radical-polar crossover’ reactions: trapping of aliphatic radicals by TTF+· Chemical Communications. 627-628. DOI: 10.1039/B000786M |
0.405 |
|
| 2000 |
Patro B, Merrett MC, Makin SD, Murphy JA, Parkes KE. Radical-polar crossover reactions with a water-soluble tetrathiafulvalene derivative Tetrahedron Letters. 41: 421-424. DOI: 10.1016/S0040-4039(99)02075-4 |
0.364 |
|
| 2000 |
Gonzalez Martin C, Murphy JA, Smith CR. Replacing tin in radical chemistry: N-ethylpiperidine hypophosphite in cyclisation reactions of aryl radicals Tetrahedron Letters. 41: 1833-1836. DOI: 10.1016/S0040-4039(00)00010-1 |
0.475 |
|
| 2000 |
Murphy JA, Scott KA, Sinclair RS, Martin CG, Kennedy AR, Lewis N. ChemInform Abstract: A Radical Based Addition-Elimination Route for the Preparation of Indoles. Cheminform. 31: no-no. DOI: 10.1002/chin.200048140 |
0.311 |
|
| 1999 |
Graham SR, Murphy JA, Kennedy AR. Hypophosphite mediated carbon–carbon bond formation: total synthesis of epialboatrin and structural revision of alboatrin Journal of the Chemical Society-Perkin Transactions 1. 3071-3073. DOI: 10.1039/A907032J |
0.37 |
|
| 1999 |
Koizumi T, Bashir N, Kennedy AR, Murphy JA. Diazadithiafulvalenes as electron donor reagents Journal of the Chemical Society-Perkin Transactions 1. 1999: 3637-3643. DOI: 10.1039/A906684E |
0.459 |
|
| 1999 |
Callaghan O, Lampard C, Kennedy AR, Murphy JA. A Novel Total Synthesis Of ()-Aspidospermidine Journal of the Chemical Society-Perkin Transactions 1. 1999: 995-1002. DOI: 10.1039/A900335E |
0.396 |
|
| 1999 |
Kizil M, Patro B, Callaghan O, Murphy JA, Hursthouse MB, Hibbs D. Tandem Radical Cyclizations on Iodoaryl Azides: Synthesis of the Core Tetracycle ofAspidospermaAlkaloids The Journal of Organic Chemistry. 64: 7856-7862. DOI: 10.1021/Jo990891X |
0.433 |
|
| 1999 |
Patro B, Merrett M, Murphy JA, Sherrington DC, Morrison MG. Radical-polar crossover reactions with polymer-supported tetrathiafulvalene Tetrahedron Letters. 40: 7857-7860. DOI: 10.1016/S0040-4039(99)01679-2 |
0.331 |
|
| 1999 |
Graham SR, Murphy JA, Coates D. Hypophosphite mediated carbon-carbon bond formation: A clean approach to radical methodology Tetrahedron Letters. 40: 2415-2416. DOI: 10.1016/S0040-4039(99)00117-3 |
0.364 |
|
| 1999 |
Callaghan O, Lampard C, Kennedy AR, Murphy JA. A novel route to (±)-aspidospermidine: First application of “radical-polar crossover” reactions to total synthesis Tetrahedron Letters. 40: 161-164. DOI: 10.1016/S0040-4039(98)80047-6 |
0.346 |
|
| 1998 |
Fletcher R, Kizil M, Lampard C, Murphy JA, Roome SJ. Tetrathiafulvalene-mediated stereoselective synthesis of the tetracyclic core of Aspidosperma alkaloids Journal of the Chemical Society-Perkin Transactions 1. 2341-2352. DOI: 10.1039/A802974A |
0.434 |
|
| 1998 |
Murphy JA, Rasheed F, Roome SJ, Scott KA, Lewis N. Intramolecular termination of radical-polar crossover reactions Journal of the Chemical Society-Perkin Transactions 1. 2331-2340. DOI: 10.1039/A802971G |
0.41 |
|
| 1997 |
Hewlins SA, Murphy JA, Lin J, Hibbs DE, Hursthouse MB. Nitration of α,β-unsaturated esters. Evidence for positivecharge build-up adjacent to carbonyl carbon Journal of the Chemical Society-Perkin Transactions 1. 1559-1570. DOI: 10.1039/A607170H |
0.379 |
|
| 1997 |
Murphy JA, Rasheed F, Gastaldi S, Ravishanker T, Lewis N. Synthesis Of Functionalised Indolines By Radical-Polar Crossover Reactions Journal of the Chemical Society-Perkin Transactions 1. 1549-1558. DOI: 10.1039/A607060D |
0.464 |
|
| 1997 |
Koizumi T, Bashir N, Murphy JA. Reactions of Arenediazonium Salts with Diazadithiafulvalenes Tetrahedron Letters. 38: 7635-7638. DOI: 10.1016/S0040-4039(97)01813-3 |
0.433 |
|
| 1997 |
Murphy JA, Scott KA, Sinclair RS, Lewis N. A new synthesis of indoles Tetrahedron Letters. 38: 7295-7298. DOI: 10.1016/S0040-4039(97)01695-X |
0.403 |
|
| 1997 |
Kizil M, Murphy JA. A new free radical route to oximes using alkyl halides, hexabutylditin and readily available nitrite esters Tetrahedron. 53: 16847-16858. DOI: 10.1016/S0040-4020(97)10086-2 |
0.314 |
|
| 1996 |
Fletcher RJ, Hibbs DE, Hursthouse M, Lampard C, Murphy JA, Roome SJ. Stereocontrolled synthesis of complex polycycles using tetrathiafulvalene mediated radical-polar crossover reactions Chemical Communications. 739-740. DOI: 10.1039/Cc9960000739 |
0.423 |
|
| 1996 |
Murphy JA, Rasheed F, Roome SJ, Lewis N. Termination of radical-polar crossover reactions by intramolecular nucleophiles Chemical Communications. 737-738. DOI: 10.1039/Cc9960000737 |
0.428 |
|
| 1996 |
Kizil M, Lampard C, Murphy JA. Studies of the tetrathiafulvalene mediated radical-polar crossover reaction directed toward the total synthesis of alkaloid natural products Tetrahedron Letters. 37: 2511-2514. DOI: 10.1016/0040-4039(96)00306-1 |
0.309 |
|
| 1995 |
Murphy JA, Roome SJ. Trapping of translocated radicals by tetrathiafulvalene radical cation Journal of the Chemical Society-Perkin Transactions 1. 1349-1358. DOI: 10.1039/P19950001349 |
0.447 |
|
| 1995 |
Batsanov AS, Begley MJ, Fletcher RJ, Murphy JA, Sherburn MS. Stereocontrol in cyclisation of dioxolanyl radicals Journal of the Chemical Society, Perkin Transactions 1. 1281-1294. DOI: 10.1039/P19950001281 |
0.371 |
|
| 1995 |
Fletcher RJ, Lampard C, Murphy JA, Lewis N. Tetrathiafulvalene: a catalyst for sequential radical–polar reactions Journal of the Chemical Society-Perkin Transactions 1. 623-633. DOI: 10.1039/P19950000623 |
0.479 |
|
| 1995 |
Kizil M, Murphy JA. Stereoselective preparation of the ABCE tetracycle of aspidospermidine and related alkaloids Journal of the Chemical Society, Chemical Communications. 1409-1410. DOI: 10.1039/C39950001409 |
0.384 |
|
| 1995 |
Hewlins SA, Murphy JA, Lin J. Anomalous nitrations of αβ-unsaturated esters: a role for α-carbonyl cations? Journal of the Chemical Society, Chemical Communications. 559-560. DOI: 10.1039/C39950000559 |
0.323 |
|
| 1994 |
Begley MJ, Murphy JA, Roome SJ. Tetrathiafulvalene as a trigger for sequential radical translocation and functionalisation Tetrahedron Letters. 35: 8679-8682. DOI: 10.1016/S0040-4039(00)78470-X |
0.302 |
|
| 1994 |
Hussain N, Morgan DO, White CR, Murphy JA. Alkoxy radicals in organic synthesis. A novel approach to a key intermediate in milbemycin chemistry Tetrahedron Letters. 35: 5069-5072. DOI: 10.1016/S0040-4039(00)73322-3 |
0.355 |
|
| 1993 |
Breen AP, Murphy JA. Vinyl epoxides: reagents for radical-induced DNA cleavage Journal of the Chemical Society-Perkin Transactions 1. 2979-2990. DOI: 10.1039/P19930002979 |
0.373 |
|
| 1993 |
Murphy JA, Patterson CW. Regioselectivity of radical-induced bond cleavages in epoxides Journal of the Chemical Society-Perkin Transactions 1. 405-410. DOI: 10.1039/P19930000405 |
0.413 |
|
| 1993 |
Begley MJ, Fletcher RJ, Murphy JA, Sherburn MS. Stereochemical control in cyclisation to bicyclic dioxolanes Journal of the Chemical Society, Chemical Communications. 1723-1725. DOI: 10.1039/C39930001723 |
0.417 |
|
| 1993 |
Lampard C, Murphy JA, Lewis N. Tetrathiafulvalene as a catalyst for radical–polar crossover reactions Journal of the Chemical Society, Chemical Communications. 295-297. DOI: 10.1039/C39930000295 |
0.409 |
|
| 1993 |
Breen AP, Murphy JA. Radical-induced DNA cleavage mediated by a vinyl expoxide Journal of the Chemical Society, Chemical Communications. 193-194. DOI: 10.1039/C39930000193 |
0.35 |
|
| 1993 |
Breen AP, Murphy JA. Modelling radical-initiated DNA cleavage by vinyl epoxides Journal of the Chemical Society, Chemical Communications. 191-192. DOI: 10.1039/C39930000191 |
0.395 |
|
| 1992 |
Hewlins SA, Murphy JA. Chapter 4. Reaction mechanisms. Part (iii) Free-radical reactions Annual Reports Section "B" (Organic Chemistry). 89: 75. DOI: 10.1039/OC9928900075 |
0.316 |
|
| 1992 |
Dickinson JM, Murphy JA. Pyrrolidines and allylic amines from radical-induced cleavage of aziridines Tetrahedron. 48: 1317-1326. DOI: 10.1016/S0040-4020(01)90793-8 |
0.635 |
|
| 1991 |
Begley MJ, Housden N, Johns A, Murphy JA. Intramolecular reactions of allyloxy radicals featuring six-centred transition states; Regiochemistry and stereochemistry. Tetrahedron. 47: 8417-8430. DOI: 10.1016/S0040-4020(01)96183-6 |
0.344 |
|
| 1990 |
Dickinson JM, Murphy JA, Patterson CW, Wooster NF. A novel probe for free radicals featuring epoxide cleavage Journal of the Chemical Society-Perkin Transactions 1. 1179-1184. DOI: 10.1039/P19900001179 |
0.448 |
|
| 1990 |
Murphy JA, Sherburn MS, Dickinson JM, Goodman C. A controlled balance between ionic and radical pathways in reactions of tributyltin hydride Journal of the Chemical Society, Chemical Communications. 1069-1070. DOI: 10.1039/C39900001069 |
0.654 |
|
| 1990 |
Dickinson JM, Murphy JA. Regiospecific radical-induced cleavage of aziridines: Syntheses of allylic amines and pyrrolidines Journal of the Chemical Society, Chemical Communications. 434-436. DOI: 10.1039/C39900000434 |
0.677 |
|
| 1990 |
Murphy JA, Sherburn MS. Intramolecular free-radical substitution reactions of pyridinium rings: Efficient formation of [5,6]- and [6,7]-fused ring systems. Tetrahedron Letters. 31: 3495-3496. DOI: 10.1016/S0040-4039(00)97432-X |
0.332 |
|
| 1990 |
Murphy JA, Dickinson JM, Sherburn MS, Patterson CW, Wooster NF. A study of chemical reactions which report the presence of free-radicals Free Radical Biology and Medicine. 9: 61. DOI: 10.1016/0891-5849(90)90386-W |
0.666 |
|
| 1990 |
Murphy JA, Sherburn MS. Intramolecular addition of Free radicals to quaternised heterocyclic rings. Tetrahedron Letters. 31: 1625-1628. DOI: 10.1016/0040-4039(90)80034-J |
0.303 |
|
| 1990 |
MURPHY JA, SHERBURN MS. ChemInform Abstract: Intramolecular Addition of Free Radicals to Quaternized Heterocyclic Rings. Cheminform. 21. DOI: 10.1002/chin.199050211 |
0.313 |
|
| 1990 |
DICKINSON JM, MURPHY JA. ChemInform Abstract: Regiospecific Radical-Induced Cleavage of Aziridines: Syntheses of Allylic Amines and Pyrrolidines. Cheminform. 21. DOI: 10.1002/chin.199036219 |
0.649 |
|
| 1990 |
DICKINSON JM, MURPHY JA, PATTERSON CW, WOOSTER NF. ChemInform Abstract: A Novel Probe for Free Radicals Featuring Epoxide Cleavage. Cheminform. 21. DOI: 10.1002/chin.199030086 |
0.595 |
|
| 1990 |
JOHNS A, MURPHY JA, SHERBURN MS. ChemInform Abstract: Intramolecular Reactions of Allyloxy Radicals. Cheminform. 21. DOI: 10.1002/chin.199016121 |
0.367 |
|
| 1989 |
Murphy JA, Sherburn MS. Chapter 4. Reaction mechanisms. Part (iii) Free radicals Annual Reports Section "B" (Organic Chemistry). 86: 73. DOI: 10.1039/OC9898600073 |
0.309 |
|
| 1989 |
Johns A, Murphy JA, Sherburn MS. Intramolecular reactions of allyloxy radicals Tetrahedron. 45: 7835-7858. DOI: 10.1016/S0040-4020(01)85798-7 |
0.357 |
|
| 1988 |
Murphy JA, Patterson CW, Wooster NF. Modelling vinyl ether formation in rifamycin S Journal of the Chemical Society, Chemical Communications. 4: 294-296. DOI: 10.1039/C39880000294 |
0.311 |
|
| 1987 |
Johns A, Murphy JA, Patterson CW, Wooster NF. A novel probe for free-radical intermediates Journal of the Chemical Society, Chemical Communications. 1238-1240. DOI: 10.1039/C39870001238 |
0.375 |
|
| 1986 |
Cook M, Hares O, Johns A, Murphy JA, Patterson CW. Novel synthesis of vinyl ethers induced by carbon–halogen bond homolysis Journal of the Chemical Society, Chemical Communications. 1419-1420. DOI: 10.1039/C39860001419 |
0.383 |
|
| 1980 |
MURPHY JA, STAUNTON J. ChemInform Abstract: NOVEL SYNTHESIS OF PRETETRAMID Chemischer Informationsdienst. 11. DOI: 10.1002/Chin.198017196 |
0.52 |
|
| 1980 |
MURPHY JA, STAUNTON J. ChemInform Abstract: A NOVEL BASE-INDUCED CYCLIZATION TO PRODUCE AN ARYL RING Chemischer Informationsdienst. 11. DOI: 10.1002/chin.198017189 |
0.503 |
|
| 1979 |
Murphy JA, Staunton J. Novel synthesis of pretetramid Journal of the Chemical Society, Chemical Communications. 1166-1167. DOI: 10.1039/C39790001166 |
0.509 |
|
| 1979 |
Murphy JA, Staunton J. A novel base-induced cyclisation to produce an aryl ring Journal of the Chemical Society, Chemical Communications. 1165-1166. DOI: 10.1039/C39790001165 |
0.539 |
|
| 1979 |
Evans GE, Leeper FJ, Murphy JA, Staunton J. Triacetic acid lactone as a polyketide synthon: Synthesis of toralactone and polyketide-type anthracene derivatives Journal of the Chemical Society, Chemical Communications. 205-206. DOI: 10.1039/C39790000205 |
0.508 |
|
| 1979 |
EVANS GE, LEEPER FJ, MURPHY JA, STAUNTON J. ChemInform Abstract: TRIACETIC ACID LACTONE AS A POLYKETIDE SYNTHON: SYNTHESIS OF TORALACTONE AND POLYKETIDE-TYPE ANTHRACENE DERIVATIVES Chemischer Informationsdienst. 10. DOI: 10.1002/Chin.197945225 |
0.522 |
|
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