| Year |
Citation |
Score |
| 2022 |
Zhong Z, Chesti J, Armstrong A, Bull JA. Synthesis of Sulfoximine Propargyl Carbamates under Improved Conditions for Rhodium Catalyzed Carbamate Transfer to Sulfoxides. The Journal of Organic Chemistry. PMID 36379008 DOI: 10.1021/acs.joc.2c02083 |
0.648 |
|
| 2021 |
Jamshidiha M, Lanyon-Hogg T, Sutherell CL, Craven GB, Tersa M, De Vita E, Brustur D, Pérez-Dorado I, Hassan S, Petracca R, Morgan RM, Sanz-Hernández M, Norman JC, Armstrong A, Mann DJ, et al. Identification of the first structurally validated covalent ligands of the small GTPase RAB27A. Rsc Medicinal Chemistry. 13: 150-155. PMID 35308027 DOI: 10.1039/d1md00225b |
0.454 |
|
| 2021 |
Craven GB, Briggs EL, Zammit CM, McDermott A, Greed S, Affron DP, Leinfellner C, Cudmore HR, Tweedy RR, Luisi R, Bull JA, Armstrong A. Synthesis and Configurational Assignment of Vinyl Sulfoximines and Sulfonimidamides. The Journal of Organic Chemistry. PMID 34003635 DOI: 10.1021/acs.joc.1c00373 |
0.616 |
|
| 2019 |
Craven GB, Affron DP, Raymond PN, Mann DJ, Armstrong A. Vinyl sulfonamide synthesis for irreversible tethering a novel α-selenoether protection strategy. Medchemcomm. 10: 158-163. PMID 30774862 DOI: 10.1039/C8Md00566D |
0.375 |
|
| 2018 |
Craven G, Affron D, Allen C, Matthies S, Greener J, Morgan R, Tate E, Armstrong A, Mann DJ. High-Throughput Kinetic Analysis for Target-Directed Covalent Ligand Discovery. Angewandte Chemie (International Ed. in English). PMID 29480525 DOI: 10.1002/Anie.201711825 |
0.517 |
|
| 2016 |
Burés J, Armstrong A, Blackmond DG. Explaining Anomalies in Enamine Catalysis: "Downstream Species" as a New Paradigm for Stereocontrol. Accounts of Chemical Research. PMID 26830669 DOI: 10.1021/Acs.Accounts.5B00394 |
0.394 |
|
| 2016 |
Armstrong A, Pullin RDC, Scutt JN. Tertiary Amine Promoted Aziridination: Preparation of NH-Aziridines from Aliphatic α,β-Unsaturated Ketones Synlett. 27: 151-155. DOI: 10.1055/S-0035-1560583 |
0.354 |
|
| 2016 |
Sung S, Sale D, Braddock DC, Armstrong A, Brennan C, Davies RP. Mechanistic Studies on the Copper-Catalyzed N-Arylation of Alkylamines Promoted by Organic Soluble Ionic Bases Acs Catalysis. 6: 3965-3974. DOI: 10.1021/Acscatal.6B00504 |
0.719 |
|
| 2015 |
Sung S, Braddock DC, Armstrong A, Brennan C, Sale D, White AJ, Davies RP. Synthesis, characterisation and reactivity of copper(I) amide complexes and studies on their role in the modified Ullmann amination reaction. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 7179-92. PMID 25788223 DOI: 10.1002/Chem.201405699 |
0.7 |
|
| 2015 |
Leung W, Shaffer CD, Reed LK, Smith ST, Barshop W, Dirkes W, Dothager M, Lee P, Wong J, Xiong D, Yuan H, Bedard JE, Machone JF, Patterson SD, Price AL, ... ... Armstrong AR, et al. Drosophila muller f elements maintain a distinct set of genomic properties over 40 million years of evolution. G3 (Bethesda, Md.). 5: 719-40. PMID 25740935 DOI: 10.1534/G3.114.015966 |
0.33 |
|
| 2015 |
Allen CE, Curran PR, Brearley AS, Boissel V, Sviridenko L, Press NJ, Stonehouse JP, Armstrong A. Efficient and facile synthesis of acrylamide libraries for protein-guided tethering. Organic Letters. 17: 458-60. PMID 25582165 DOI: 10.1021/Ol503486T |
0.364 |
|
| 2014 |
Burés J, Dingwall P, Armstrong A, Blackmond DG. Rationalization of an unusual solvent-induced inversion of enantiomeric excess in organocatalytic selenylation of aldehydes. Angewandte Chemie (International Ed. in English). 53: 8700-4. PMID 25044727 DOI: 10.1002/Anie.201404327 |
0.396 |
|
| 2014 |
Armstrong A, Emmerson DP, Milner HJ, Sheppard RJ. [2,3]-Sigmatropic rearrangement of allylic selenimides: strategy for the synthesis of peptides, peptidomimetics, and N-aryl vinyl glycines. The Journal of Organic Chemistry. 79: 3895-907. PMID 24684633 DOI: 10.1021/Jo500341E |
0.329 |
|
| 2014 |
Armstrong A, Pullin RDC, Jenner CR, Foo K, White AJP, Scutt JN. Tertiary amine-promoted enone aziridination: Investigations into factors influencing enantioselective induction Tetrahedron Asymmetry. 25: 74-86. DOI: 10.1016/J.Tetasy.2013.11.008 |
0.384 |
|
| 2013 |
Struebing H, Ganase Z, Karamertzanis PG, Siougkrou E, Haycock P, Piccione PM, Armstrong A, Galindo A, Adjiman CS. Computer-aided molecular design of solvents for accelerated reaction kinetics. Nature Chemistry. 5: 952-7. PMID 24153374 DOI: 10.1038/Nchem.1755 |
0.346 |
|
| 2013 |
Burés J, Armstrong A, Blackmond DG. The interplay of thermodynamics and kinetics in dictating organocatalytic reactivity and selectivity Pure and Applied Chemistry. 85: 1919-1934. DOI: 10.1351/Pac-Con-13-01-14 |
0.381 |
|
| 2013 |
Armstrong A, Braddock DC, Jones AX, Clark S. Catalytic asymmetric bromolactonization reactions using (DHQD)2PHAL-benzoic acid combinations Tetrahedron Letters. 54: 7004-7008. DOI: 10.1016/J.Tetlet.2013.10.043 |
0.369 |
|
| 2012 |
Armstrong A, Ferguson A. Synthesis and ring openings of cinnamate-derived N-unfunctionalised aziridines. Beilstein Journal of Organic Chemistry. 8: 1747-52. PMID 23209508 DOI: 10.3762/Bjoc.8.199 |
0.377 |
|
| 2012 |
Burés J, Armstrong A, Blackmond DG. Curtin-Hammett paradigm for stereocontrol in organocatalysis by diarylprolinol ether catalysts. Journal of the American Chemical Society. 134: 6741-50. PMID 22452319 DOI: 10.1021/Ja300415T |
0.394 |
|
| 2012 |
Burés J, Armstrong A, Blackmond DG. Kinetic correlation between aldehyde/enamine stereoisomers in reactions between aldehydes with α -stereocenters and chiral pyrrolidine-based catalysts Chemical Science. 3: 1273-1277. DOI: 10.1039/C2Sc01082H |
0.409 |
|
| 2011 |
Hein JE, Burés J, Lam YH, Hughes M, Houk KN, Armstrong A, Blackmond DG. Enamine carboxylates as stereodetermining intermediates in prolinate catalysis. Organic Letters. 13: 5644-7. PMID 21958394 DOI: 10.1021/Ol2023533 |
0.392 |
|
| 2011 |
Hein JE, Armstrong A, Blackmond DG. Kinetic profiling of prolinate-catalyzed α-amination of aldehydes Organic Letters. 13: 4300-4303. PMID 21761822 DOI: 10.1021/Ol201639Z |
0.383 |
|
| 2011 |
Burés J, Armstrong A, Blackmond DG. Mechanistic rationalization of organocatalyzed conjugate addition of linear aldehydes to nitro-olefins. Journal of the American Chemical Society. 133: 8822-5. PMID 21568340 DOI: 10.1021/Ja203660R |
0.394 |
|
| 2011 |
Armstrong A, Emmerson DP. Enantioselective synthesis of α-alkyl,α-vinyl amino acids via [2,3]-sigmatropic rearrangement of selenimides. Organic Letters. 13: 1040-3. PMID 21275415 DOI: 10.1021/Ol1030926 |
0.352 |
|
| 2011 |
Armstrong A, Deacon N, Donald C. Enantioselective synthesis of -aminophosphonates via organocatalytic sulfenylation and [2,3]-sigmatropic sulfimide rearrangement Synlett. 2347-2350. DOI: 10.1055/S-0030-1260309 |
0.419 |
|
| 2010 |
Armstrong A, Pullin RD, Jenner CR, Scutt JN. Amine-promoted synthesis of vinyl aziridines. The Journal of Organic Chemistry. 75: 3499-502. PMID 20465292 DOI: 10.1021/Jo100407S |
0.348 |
|
| 2010 |
Blackmond DG, Moran A, Hughes M, Armstrong A. Unusual reversal of enantioselectivity in the proline-mediated α-amination of aldehydes induced by tertiary amine additives Journal of the American Chemical Society. 132: 7598-7599. PMID 20465280 DOI: 10.1021/Ja102718X |
0.364 |
|
| 2010 |
Armstrong A, Collins JC. Direct azole amination: C-H functionalization as a new approach to biologically important heterocycles. Angewandte Chemie (International Ed. in English). 49: 2282-5. PMID 20186895 DOI: 10.1002/Anie.200906750 |
0.301 |
|
| 2010 |
Blackmond DG, Moran A, Hughes M, Armstrong A. Inversion of Enantioselectivity in Proline Catalysis by BasicAdditives Synfacts. 2010: 950-950. DOI: 10.1055/S-0030-1257799 |
0.378 |
|
| 2010 |
Armstrong A, Bettati M, White AJ. Catalytic enantioselective alkene epoxidation using novel spirocyclic N-carbethoxy-azabicyclo[3.2.1]octanones Tetrahedron. 66: 6309-6320. DOI: 10.1016/J.Tet.2010.04.004 |
0.385 |
|
| 2010 |
LEY SV, ARMSTRONG A. ChemInform Abstract: The Champagne Route to Avermectins and Milbemycins Cheminform. 23: no-no. DOI: 10.1002/chin.199230271 |
0.316 |
|
| 2009 |
Armstrong A, Bhonoah Y, White AJ. Constrained beta-proline analogues in organocatalytic aldol reactions: the influence of acid geometry. The Journal of Organic Chemistry. 74: 5041-8. PMID 19485343 DOI: 10.1021/Jo900840V |
0.369 |
|
| 2009 |
Zotova N, Broadbelt LJ, Armstrong A, Blackmond DG. Kinetic and mechanistic studies of proline-mediated direct intermolecular aldol reactions Bioorganic and Medicinal Chemistry Letters. 19: 3934-3937. PMID 19362473 DOI: 10.1016/J.Bmcl.2009.03.112 |
0.361 |
|
| 2009 |
Armstrong A, Emmerson DP. Enantioselective synthesis of allenamides via sulfimide [2,3]-sigmatropic rearrangement. Organic Letters. 11: 1547-50. PMID 19254002 DOI: 10.1021/Ol900146S |
0.379 |
|
| 2009 |
Armstrong A, Pyrkotis C. Synthetic studies on amphidinolides C and F: synthesis of the C18–C29 segment of amphidinolide F Tetrahedron Letters. 50: 3325-3328. DOI: 10.1016/J.Tetlet.2009.02.093 |
0.31 |
|
| 2009 |
Armstrong A, Ashraff C, Chung H, Murtagh L. Oxidative rearrangement of 2-alkoxy-3,4-dihydro-2H-pyrans: stereocontrolled synthesis of 4,5-cis-disubstituted tetrahydrofuranones including whisky and cognac lactones and crobarbatic acid Tetrahedron. 65: 4490-4504. DOI: 10.1016/J.Tet.2009.04.013 |
0.31 |
|
| 2009 |
Zotova N, Moran A, Armstrong A, Blackmond DG. A coherent mechanistic rationale for additive effects and autoinductive behaviour in proline-mediated reactions Advanced Synthesis and Catalysis. 351: 2765-2769. DOI: 10.1002/Adsc.200900665 |
0.361 |
|
| 2008 |
Armstrong A, Bhonoah Y, Shanahan SE. Syntheses of ()-Epibatidine and ()-Epiboxidine Synfacts. 2008: 224-224. DOI: 10.1055/S-2008-1042662 |
0.317 |
|
| 2007 |
Zotova N, Franzke A, Armstrong A, Blackmond DG. Clarification of the role of water in proline-mediated aldol reactions Journal of the American Chemical Society. 129: 15100-15101. PMID 18001021 DOI: 10.1021/Ja0738881 |
0.326 |
|
| 2007 |
Armstrong A, Geldart SP, Jenner CR, Scutt JN. Organocatalytic synthesis of beta-alkylaspartates via beta-lactone ring opening. The Journal of Organic Chemistry. 72: 8091-4. PMID 17880243 DOI: 10.1021/Jo701461T |
0.319 |
|
| 2007 |
Armstrong A, Bhonoah Y, Shanahan SE. Aza-Prins-pinacol approach to 7-azabicyclo[2.2.1]heptanes: syntheses of (+/-)-epibatidine and (+/-)-epiboxidine. The Journal of Organic Chemistry. 72: 8019-24. PMID 17867705 DOI: 10.1021/Jo701536A |
0.317 |
|
| 2007 |
Armstrong A, Challinor L, Moir JH. Exploiting organocatalysis: enantioselective synthesis of vinyl glycines by allylic sulfimide [2,3] sigmatropic rearrangement. Angewandte Chemie (International Ed. in English). 46: 5369-72. PMID 17562549 DOI: 10.1002/Anie.200701459 |
0.431 |
|
| 2007 |
Armstrong A, Baxter CA, Lamont SG, Pape AR, Wincewicz R. Amine-promoted, organocatalytic aziridination of enones. Organic Letters. 9: 351-3. PMID 17217302 DOI: 10.1021/Ol062852V |
0.365 |
|
| 2007 |
Armstrong A, Challinor L, Moir JH. Concise Synthesis of Vinyl Glycines Synfacts. 2007: 868-868. DOI: 10.1055/S-2007-968750 |
0.391 |
|
| 2006 |
Mathew SP, Klussmann M, Iwamura H, Wells DH, Armstrong A, Blackmond DG. A mechanistic rationalization of unusual kinetic behavior in proline-mediated C-O and C-N bond-forming reactions. Chemical Communications (Cambridge, England). 4291-3. PMID 17047844 DOI: 10.1039/B609926B |
0.373 |
|
| 2006 |
Klussmann M, Iwamura H, Mathew SP, Wells DH, Pandya U, Armstrong A, Blackmond DG. Thermodynamic control of asymmetric amplification in amino acid catalysis Nature. 441: 621-623. PMID 16738656 DOI: 10.1038/Nature04780 |
0.402 |
|
| 2006 |
Armstrong A, Challinor L, Cooke RS, Moir JH, Treweeke NR. Oxaziridine-mediated amination of branched allylic sulfides: stereospecific formation of allylic amine derivatives via [2,3]-sigmatropic rearrangement. The Journal of Organic Chemistry. 71: 4028-30. PMID 16674092 DOI: 10.1021/Jo060369S |
0.411 |
|
| 2006 |
Armstrong A, Convine NJ, Popkin ME. Diastereoselective Conjugate Addition of Cyanide to α,β-Unsaturated Oxazolidinones: Enantioselective Synthesis of ent-Pregabalin and Baclofen Synlett. 2006: 1589-1591. DOI: 10.1055/S-2006-941584 |
0.344 |
|
| 2006 |
Armstrong A, Dominguez-Fernandez B, Tsuchiya T. Bicyclo[3.2.1]octanone catalysts for asymmetric alkene epoxidation: the effect of disubstitution Tetrahedron. 62: 6614-6620. DOI: 10.1016/J.Tet.2005.12.073 |
0.33 |
|
| 2006 |
Armstrong A, Tsuchiya T. A new class of chiral tetrahydropyran-4-one catalyst for asymmetric epoxidation of alkenes Tetrahedron. 62: 257-263. DOI: 10.1016/J.Tet.2005.08.112 |
0.35 |
|
| 2005 |
Armstrong A, Shanahan SE. aza-Prins-pinacol approach to 7-azabicyclo[2.2.1]heptanes and ring expansion to [3.2.1]tropanes. Organic Letters. 7: 1335-8. PMID 15787500 DOI: 10.1021/Ol0501267 |
0.388 |
|
| 2005 |
Armstrong A, Jones LH, Knight JD, Kelsey RD. Oxaziridine-mediated amination of primary amines: scope and application to a one-pot pyrazole synthesis. Organic Letters. 7: 713-6. PMID 15704932 DOI: 10.1021/Ol0474507 |
0.434 |
|
| 2005 |
Armstrong A, Edmonds ID, Swarbrick ME. Heteroatom transfer to alkenes by N-protected-oxaziridines : new reaction pathways and products Tetrahedron Letters. 46: 2207-2210. DOI: 10.1016/J.Tetlet.2005.02.034 |
0.348 |
|
| 2005 |
Armstrong A, Edmonds ID, Swarbrick ME, Treweeke NR. Electrophilic amination of enolates with oxaziridines: effects of oxaziridine structure and reaction conditions Tetrahedron. 61: 8423-8442. DOI: 10.1016/J.Tet.2005.06.085 |
0.397 |
|
| 2005 |
Armstrong A, Shanahan SE, Edmonds I, Knight JD, Cooke RS, Cumming GR. New methods and synthetic applications of asymmetric nitrogen transfer Chinese Journal of Chemistry. 23: 1270-1272. DOI: 10.1002/Cjoc.200591270 |
0.4 |
|
| 2004 |
Armstrong A, Cumming GR, Pike K. Aminative rearrangement of 2-alkoxy-3,4-dihydro-2H-pyrans: a novel stereocontrolled route to substituted pyrrolidines. Chemical Communications (Cambridge, England). 812-3. PMID 15045076 DOI: 10.1039/B316554J |
0.329 |
|
| 2004 |
Armstrong A. Amine-catalyzed epoxidation of alkenes: a new mechanism for the activation of oxone. Angewandte Chemie (International Ed. in English). 43: 1460-2. PMID 15022213 DOI: 10.1002/Anie.200301716 |
0.333 |
|
| 2004 |
Armstrong A, Scutt JN. Total synthesis of (+)-belactosin A. Chemical Communications (Cambridge, England). 510-1. PMID 14973582 DOI: 10.1039/B316142K |
0.341 |
|
| 2004 |
Armstrong A, Gethin DM, Wheelhouse CJ. Furanose synthesis via regioselective dihydroxylation of 1-silyloxy-1,3-dienes: Application to the furanose unit of 4-epi-hygromycin A Synlett. 2004: 350-352. DOI: 10.1055/S-2003-44979 |
0.385 |
|
| 2003 |
Armstrong A, Cooke RS, Shanahan SE. Amination and [2,3]-sigmatropic rearrangement of propargylic sulfides using a ketomalonate-derived oxaziridine: synthesis of N-allenylsulfenimides. Organic & Biomolecular Chemistry. 1: 3142-3. PMID 14527143 DOI: 10.1039/B307722E |
0.318 |
|
| 2003 |
Washington I, Houk KN, Armstrong A. Strategies for the design of organic aziridination reagents and catalysts: transition structures for alkene aziridinations by NH transfer. The Journal of Organic Chemistry. 68: 6497-501. PMID 12919009 DOI: 10.1021/Jo034415P |
0.305 |
|
| 2003 |
Armstrong A, Scutt JN. Stereocontrolled synthesis of 3-(trans-2-aminocyclopropyl)alanine, a key component of belactosin A. Organic Letters. 5: 2331-4. PMID 12816441 DOI: 10.1021/Ol0346887 |
0.451 |
|
| 2003 |
Sartori G, Armstrong A, Maggi R, Mazzacani A, Sartorio R, Bigi F, Dominguez-Fernandez B. Alpha-fluorotropinone immobilized on silica: a new stereoselective heterogeneous catalyst for epoxidation of alkenes with oxone. The Journal of Organic Chemistry. 68: 3232-7. PMID 12688795 DOI: 10.1021/Jo034044C |
0.347 |
|
| 2003 |
Armstrong A, Edmonds ID, Swarbrick ME. Efficient nitrogen transfer from aldehyde-derived N-acyloxaziridines Tetrahedron Letters. 44: 5335-5338. DOI: 10.1016/S0040-4039(03)01200-0 |
0.358 |
|
| 2003 |
Armstrong A, Davies NGM, Martin NG, Rutherford AP. Evaluation of asymmetric Diels–Alder approaches for the synthesis of the cyclohexene subunit of CP-225,917 and CP-263,114 Tetrahedron Letters. 44: 3915-3918. DOI: 10.1016/S0040-4039(03)00835-9 |
0.423 |
|
| 2003 |
Armstrong A, Barsanti PA, Blench TJ, Ogilvie R. Synthesis of the C1-side chain of zaragozic acid D and progress towards a total synthesis Tetrahedron. 59: 367-375. DOI: 10.1016/S0040-4020(02)01514-4 |
0.408 |
|
| 2002 |
Armstrong A, Ahmed G, Dominguez-Fernandez B, Hayter BR, Wailes JS. Enantioselective epoxidation of alkenes catalyzed by 2-fluoro-N-carbethoxytropinone and related tropinone derivatives. The Journal of Organic Chemistry. 67: 8610-7. PMID 12444645 DOI: 10.1021/Jo026322Y |
0.391 |
|
| 2002 |
Armstrong A, Cooke RS. Efficient amination of sulfides with a ketomalonate-derived oxaziridine: application to [2,3]-sigmatropic rearrangements of allylic sulfimides. Chemical Communications (Cambridge, England). 904-5. PMID 12123037 DOI: 10.1039/B201791A |
0.375 |
|
| 2002 |
Armstrong A, Critchley TJ, Gourdel-Martin M, Kelsey RD, Mortlock AA. Synthetic studies on CP-225,917 and CP-263,114: concise synthesis of the bicyclic core using an intramolecular Mukaiyama aldol reaction Journal of the Chemical Society-Perkin Transactions 1. 1344-1350. DOI: 10.1039/B202752F |
0.422 |
|
| 2001 |
Armstrong A, Draffan AG. Intramolecular epoxidation in unsaturated ketones and oxaziridines Journal of the Chemical Society-Perkin Transactions 1. 2861-2873. DOI: 10.1039/B107839A |
0.366 |
|
| 2001 |
Armstrong A, Moss WO, Reeves JR. Asymmetric epoxidation catalyzed by esters of α-hydroxy-8-oxabicyclo[3.2.1]octan-3-one Tetrahedron: Asymmetry. 12: 2779-2781. DOI: 10.1016/S0957-4166(01)00495-5 |
0.356 |
|
| 2001 |
Armstrong A, Atkin MA, Swallow S. Asymmetric electrophilic amination of enolates by a chiral N-alkoxycarbonyloxaziridine Tetrahedron: Asymmetry. 12: 535-538. DOI: 10.1016/S0957-4166(01)00104-5 |
0.382 |
|
| 2001 |
Armstrong A, Goldberg FW, Sandham DA. Corrigendum to “A one-step synthesis of tetrahydropyranopyranones from carbonyl compounds” Tetrahedron Letters. 42: 8399. DOI: 10.1016/S0040-4039(01)01805-6 |
0.394 |
|
| 2001 |
Armstrong A, Goldberg FW, Sandham DA. A one-step synthesis of tetrahydropyranopyranones from carbonyl compounds Tetrahedron Letters. 42: 4585-4587. DOI: 10.1016/S0040-4039(01)00803-6 |
0.351 |
|
| 2000 |
Armstrong A, Barsanti PA, Jones LH, Ahmed G. Total synthesis of (+)-zaragozic acid C. The Journal of Organic Chemistry. 65: 7020-32. PMID 11031024 DOI: 10.1021/Jo000700M |
0.398 |
|
| 2000 |
Armstrong A, Hayter BR, Moss WO, Reeves JR, Wailes J. Alkene epoxidation catalyzed by bicyclo[3.2.1]octan-3-ones: effects of structural modifications on catalyst efficiency and epoxidation enantioselectivity Tetrahedron: Asymmetry. 11: 2057-2061. DOI: 10.1016/S0957-4166(00)00170-1 |
0.371 |
|
| 2000 |
Armstrong A, Atkin MA, Swallow S. Electrophilic amination of carbanions by N-carboxamido oxaziridines Tetrahedron Letters. 41: 2247-2251. DOI: 10.1016/S0040-4039(00)00140-4 |
0.388 |
|
| 1999 |
Armstrong A, Draffan AG. Highly stereoselective intramolecular epoxidation in unsaturated oxaziridines Tetrahedron Letters. 40: 4453-4456. DOI: 10.1016/S0040-4039(99)00771-6 |
0.37 |
|
| 1999 |
Armstrong A, Hayter BR. α-Functionalised ketones as promoters of alkene epoxidation by Oxone® Tetrahedron. 55: 11119-11126. DOI: 10.1016/S0040-4020(99)00616-X |
0.382 |
|
| 1999 |
Armstrong A, Ahmed G, Garnett I, Goacolou K, Wailes J. Exocyclic iminium salts as catalysts for alkene epoxidation by Oxone® Tetrahedron. 55: 2341-2352. DOI: 10.1016/S0040-4020(99)00014-9 |
0.356 |
|
| 1998 |
Armstrong A, Draffan AG. Intramolecular Epoxidation of Unsaturated Oxaziridines Synlett. 1998: 646-648. DOI: 10.1055/S-1998-1733 |
0.422 |
|
| 1998 |
Armstrong A, Critchley TJ, Mortlock AA. Synthesis of the Bicyclo[4.4.1]decenone Core of CP-225,917 and CP-263,114 Synlett. 1998: 552-553. DOI: 10.1055/S-1998-1699 |
0.329 |
|
| 1998 |
Armstrong A. Catalytic enantioselective epoxidation of alkenes with a tropinone-derived chiral ketone Chemical Communications. 621-622. DOI: 10.1039/A708695D |
0.391 |
|
| 1998 |
Armstrong A, Jones LH, Barsanti PA. Total synthesis of (+)-zaragozic acid C Tetrahedron Letters. 39: 3337-3340. DOI: 10.1016/S0040-4039(98)00485-7 |
0.338 |
|
| 1997 |
Armstrong A, Ahmed G, Garnett I, Goacolou K. Pyrrolidine-Derived Iminium Salts As Catalysts For Alkene Epoxidation By Oxone Synlett. 1997: 1075-1076. DOI: 10.1055/S-1997-1542 |
0.336 |
|
| 1997 |
Armstrong A, Hayter BR. Concise synthesis of (4S,5S)-4,5-(isopropylidenedioxy)-2-cyclopentenone and a novel C2-symmetric ketone Tetrahedron: Asymmetry. 8: 1677-1684. DOI: 10.1016/S0957-4166(97)00153-5 |
0.398 |
|
| 1996 |
Armstrong A, Barsanti PA, Clarke PA, Wood A. Ketone-directed peracid epoxidation of cyclic alkenes Journal of the Chemical Society - Perkin Transactions 1. 1373-1380. DOI: 10.1039/P19960001373 |
0.563 |
|
| 1996 |
Armstrong A, Clarke PA, Wood A. Evidence that a dioxirane is not responsible for alkene epoxidation in a ketone–Oxone® system Chemical Communications. 849-850. DOI: 10.1039/Cc9960000849 |
0.486 |
|
| 1995 |
Armstrong A, Barsanti PA. Synthesis of the Bicyclic Core of the Zaragozic Acids (Squalestatins) Synlett. 1995: 903-906. DOI: 10.1055/S-1995-5130 |
0.318 |
|
| 1994 |
Burger MT, Armstrong A, Guarnieri F, M DQ, Still WC. Free energy calculations in molecular design: Predictions by theory and reality by experiment with enantioselective podand ionophores Journal of the American Chemical Society. 116: 3593-3594. DOI: 10.1021/Ja00087A053 |
0.486 |
|
| 1992 |
Armstrong A, Still WC. Enantioselective cation binding with a functionalized podand ionophore Journal of Organic Chemistry. 57: 4580-4582. DOI: 10.1021/Jo00043A010 |
0.511 |
|
| 1991 |
Ley SV, Armstrong A, Díez-Martín D, Ford MJ, Grice P, Knight JG, Kolb HC, Madin A, Marby CA, Mukherjee S, Shaw AN, Slawin AMZ, Vile S, White AD, Williams DJ, et al. Total synthesis of the anthelmintic macrolide avermectin B1a Journal of the Chemical Society-Perkin Transactions 1. 667-692. DOI: 10.1039/P19910000667 |
0.673 |
|
| 1990 |
Armstrong A, Ley SV, Madin A, Mukherjee S. Total Synthesis of Avermectin B1a: Final Coupling Reactions and the Total Synthesis of Avermectin B1a Aglycone Synlett. 1990: 328-330. DOI: 10.1055/S-1990-21080 |
0.513 |
|
| 1990 |
Armstrong A, Ley SV. Total Synthesis of Avermectin B1a: Planning of the Synthesis and Preparation of the C1-C10 "Southern" Hydrobenzofuran Fragment Synlett. 1990: 323-325. DOI: 10.1055/S-1990-21078 |
0.46 |
|
| 1989 |
Anthony NJ, Armstrong A, Ley SV, Madin A. Total synthesis of (+)-milbemycin β1 Tetrahedron Letters. 30: 3209-3212. DOI: 10.1016/S0040-4039(00)99203-7 |
0.445 |
|
| 1989 |
Ley SV, Anthony NJ, Armstrong A, Brasca MG, Clarke T, Culshaw D, Greck C, Grice P, Jones AB, Lygo B, Madin A, Sheppard RN, Slawin AMZ, Williams DJ. A highly convergent total synthesis of the spiroacetal macrolide (+)-milbemycinβ1 Tetrahedron. 45: 7161-7194. DOI: 10.1016/S0040-4020(01)89182-1 |
0.675 |
|
| Show low-probability matches. |
