| Year |
Citation |
Score |
| 2020 |
Nouch R, Woodward S, Willcox D, Robinson D, Lewis W. Mechanistic-Insight-Driven Rate Enhancement of Asymmetric Copper-Catalyzed 1,4-Addition of Dialkylzinc Reagents to Enones Organometallics. 39: 834-840. DOI: 10.1021/Acs.Organomet.0C00005 |
0.647 |
|
| 2018 |
Al-Jumaili MA, Woodward S. Syntheses of 7-substituted anthra[2,3-b]thiophene derivatives and naphtho[2,3-b:6,7-b']dithiophene. The Journal of Organic Chemistry. PMID 30088926 DOI: 10.1021/Acs.Joc.8B01770 |
0.316 |
|
| 2017 |
Woodward S, Nouch R, Cini M, Magre M, Abid M, Diéguez M, Pàmies O, Lewis W. Enantioselective Synthesis of 6,6-Disubstituted Pentafulvenes Containing a Chiral Pendant Hydroxy Group. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29083067 DOI: 10.1002/Chem.201704247 |
0.748 |
|
| 2017 |
Woodward S, Ackermann M, Ahirwar S, Burroughs L, Garrett MR, Ritchie J, Shine J, Tyril B, Simpson K, Woodward P. Straightforward Synthesis of 2- and 2,8-Substituted Tetracenes. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28417523 DOI: 10.1002/Chem.201701170 |
0.332 |
|
| 2017 |
Willcox D, Nouch R, Kingsbury A, Robinson D, Carey JV, Brough S, Woodward S. Kinetic Analysis of Copper(I)/Feringa-Phosphoramidite Catalyzed AlEt3 1,4-Addition to Cyclohex-2-en-1-one Acs Catalysis. 7: 6901-6908. DOI: 10.1021/Acscatal.7B02198 |
0.644 |
|
| 2017 |
Eccleshare L, Selzer S, Woodward S. An efficient synthesis of substituted chrysenes Tetrahedron Letters. 58: 393-395. DOI: 10.1016/J.Tetlet.2016.12.004 |
0.325 |
|
| 2017 |
Al-jumaili MA, Woodward S. Efficient synthesis of 2,5-dicarbonyl derivatives of 3,4-ethylenedithiothiophene (EDTT) via addition-elimination reaction Tetrahedron. 73: 5847-5852. DOI: 10.1016/J.Tet.2017.08.026 |
0.405 |
|
| 2016 |
Eccleshare L, Lozada-Rodríguez L, Cooper P, Burroughs L, Ritchie J, Lewis W, Woodward S. Diversification of ortho-Fused Cycloocta-2,5-dien-1-one Cores and Eight to Six-Ring Conversion by σ Bond C-C Cleavage. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27452351 DOI: 10.1002/Chem.201601970 |
0.406 |
|
| 2016 |
Lee DS, Durán-Peña MJ, Burroughs L, Woodward S. Efficient Preparation of TMSCCl2 Br and Its Use in Dichlorocyclopropanation of Electron-Deficient Alkenes. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27112785 DOI: 10.1002/Chem.201600607 |
0.362 |
|
| 2016 |
Cini M, Williams H, Fay MW, Searle MS, Woodward S, Bradshaw TD. Enantiopure titanocene complexes - direct evidence for paraptosis in cancer cells. Metallomics : Integrated Biometal Science. PMID 26806372 DOI: 10.1039/C5Mt00297D |
0.309 |
|
| 2016 |
Burroughs L, Ritchie J, Woodward S. Understanding anionic Chugaev elimination in pericyclic tetracene formation Tetrahedron. 72: 1686-1689. DOI: 10.1016/J.Tet.2016.02.025 |
0.343 |
|
| 2015 |
Cini M, Bradshaw TD, Woodward S, Lewis W. Asymmetric Pentafulvene Carbometalation-Access to Enantiopure Titanocene Dichlorides of Biological Relevance. Angewandte Chemie (International Ed. in English). PMID 26457574 DOI: 10.1002/Anie.201508034 |
0.441 |
|
| 2015 |
Burroughs L, Eccleshare L, Ritchie J, Kulkarni O, Lygo B, Woodward S, Lewis W. One-Pot Cannizzaro Cascade Synthesis of ortho-Fused Cycloocta-2,5-dien-1-ones from 2-Bromo(hetero)aryl Aldehydes. Angewandte Chemie (International Ed. in English). 54: 10648-51. PMID 26230528 DOI: 10.1002/Anie.201505347 |
0.395 |
|
| 2015 |
Burroughs L, Ritchie J, Ngwenya M, Khan D, Lewis W, Woodward S. Anionic sigmatropic-electrocyclic-Chugaev cascades: accessing 12-aryl-5-(methylthiocarbonylthio)tetracenes and a related anthra[2,3-b]thiophene. Beilstein Journal of Organic Chemistry. 11: 273-9. PMID 25815080 DOI: 10.3762/Bjoc.11.31 |
0.411 |
|
| 2015 |
Garcia P, Germain N, Woodward S, Alexakis A. Copper-Catalyzed Asymmetric Conjugate Addition to α-Alkylidene Cycloalkanones Synlett. 26: 901-906. DOI: 10.1055/S-0034-1380165 |
0.401 |
|
| 2015 |
Wahl B, Lee DS, Woodward S. 1,4-Addition of TMSCCl3 to (E)-Fumaric Esters and Thermal Rearrangement of the Adducts to 3,4-Dichloropent-2-enedioates European Journal of Organic Chemistry. 2015: 6033-6039. DOI: 10.1002/Ejoc.201500730 |
0.342 |
|
| 2015 |
Latham CM, Lewis W, Blake AJ, Woodward S. Expedient synthesis of homochiral 1-aryl-substituted 4,5-dihydro-1H-imidazoles and their modification to N-heterocyclic carbene precursors European Journal of Organic Chemistry. 2015: 1819-1823. DOI: 10.1002/Ejoc.201403560 |
0.44 |
|
| 2014 |
Wu N, Wahl B, Woodward S, Lewis W. 1,4-Addition of TMSCCl₃ to nitroalkenes: efficient reaction conditions and mechanistic understanding. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 7718-24. PMID 24849249 DOI: 10.1002/Chem.201402394 |
0.437 |
|
| 2014 |
Willcox D, Woodward S, Alexakis A. Enantioselective 1,4-additions of ClMeAl(CH=CHR) (R = alkyl, alkenyl, Ph) to cyclohexenones. Chemical Communications (Cambridge, England). 50: 1655-7. PMID 24400320 DOI: 10.1039/C3Cc48191C |
0.69 |
|
| 2014 |
Wahl B, Cabré A, Woodward S, Lewis W. Nucleophilic addition of TMSCCl3 to N-phosphinoyl benzaldimines: A route to N-phosphinoyl-α-(trichloromethyl)benzylamines Tetrahedron Letters. 55: 5829-5831. DOI: 10.1016/J.Tetlet.2014.08.122 |
0.327 |
|
| 2014 |
Willcox D, Gondal H, Civit MG, Woodward S. Assessing the utility of HAlCl2 derived vinylalanes for Michael addition Tetrahedron Letters. 55: 1720-1721. DOI: 10.1016/J.Tetlet.2014.01.105 |
0.677 |
|
| 2013 |
Andrews P, Latham CM, Magre M, Willcox D, Woodward S. ZrCl2(η-C5Me5)2-AlHCl2·(THF)2: efficient hydroalumination of terminal alkynes and cross-coupling of the derived alanes. Chemical Communications (Cambridge, England). 49: 1488-90. PMID 23320257 DOI: 10.1039/C2Cc37537K |
0.762 |
|
| 2013 |
Crampton RH, Fox M, Woodward S. N-(Alkylsulfamoyl)aldimines: Easily deprotected precursors for diarylmethylamine synthesis Tetrahedron Asymmetry. 24: 599-605. DOI: 10.1016/J.Tetasy.2013.04.006 |
0.367 |
|
| 2013 |
Dubois N, Glynn D, McInally T, Rhodes B, Woodward S, Irvine DJ, Dodds C. On DABAL-Me3 promoted formation of amides Tetrahedron. 69: 9890-9897. DOI: 10.1016/J.Tet.2013.08.062 |
0.339 |
|
| 2013 |
Cini M, Bradshaw TD, Lewis W, Woodward S. Cuprate addition to a 6-substituted pentafulvene - Preparation of sec-alkyl-substituted titanocene dichlorides and their biological activity European Journal of Organic Chemistry. 3997-4007. DOI: 10.1002/Ejoc.201300474 |
0.398 |
|
| 2012 |
Levy JN, Latham CM, Roisin L, Kandziora N, Di Fruscia P, White AJ, Woodward S, Fuchter MJ. The design and synthesis of novel IBiox N-heterocyclic carbene ligands derived from substituted amino-indanols. Organic & Biomolecular Chemistry. 10: 512-5. PMID 22120851 DOI: 10.1039/C1Ob06780J |
0.395 |
|
| 2012 |
Asikainen M, Woodward S. Allenyl ester precursors for 1H-inden-1-ol carboxylates: comparisons with their propargylic equivalents having terminal alkyne functions Tetrahedron. 68: 5492-5497. DOI: 10.1016/J.Tet.2012.04.086 |
0.376 |
|
| 2012 |
Latham CM, Blake AJ, Lewis W, Lawrence M, Woodward S. Short synthesis of chiral 4-substituted (S)-imidazolinium salts bearing sulfonates and their use in γ-selective reactions of allylic halides with grignard reagents European Journal of Organic Chemistry. 699-707. DOI: 10.1002/Ejoc.201101336 |
0.406 |
|
| 2011 |
Crampton R, Woodward S, Fox M. Bis-Sulfamyl Imines: Potent Substrates for Asymmetric Additions of Arylboroxines under Rhodium Catalysis Advanced Synthesis & Catalysis. 353: 903-906. DOI: 10.1002/Adsc.201000838 |
0.345 |
|
| 2011 |
Vinogradov A, Woodward S. Palladium‐Catalyzed Cross‐Coupling Using an Air‐Stable Trimethylaluminum Source. Preparation of Ethyl 4‐Methylbenzoate Organic Syntheses. 104-114. DOI: 10.1002/0471264229.Os087.12 |
0.308 |
|
| 2010 |
Hawner C, Müller D, Gremaud L, Felouat A, Woodward S, Alexakis A. Rhodium-catalyzed asymmetric 1,4-addition of aryl alanes to trisubstituted enones: binap as an effective ligand in the formation of quaternary stereocenters. Angewandte Chemie (International Ed. in English). 49: 7769-72. PMID 20821780 DOI: 10.1002/Anie.201003300 |
0.439 |
|
| 2010 |
Welker M, Woodward S, Veiros LF, Calhorda MJ. Chemoselectivity as a delineator of cuprate structure in catalytic 1,4-addition of diorganozinc reagents to Michael acceptors. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 5620-9. PMID 20391573 DOI: 10.1002/Chem.200903310 |
0.459 |
|
| 2010 |
Welker M, Woodward S, Alexakis A. Tandem reactions with chiral enolates: preparation of allylic alcohols via trapping with vinyl oxiranes. Organic Letters. 12: 576-9. PMID 20058893 DOI: 10.1021/Ol9027682 |
0.425 |
|
| 2010 |
Glynn D, Shannon J, Woodward S. On the scope of trimethylaluminum-promoted 1,2-additions of ArZnX reagents to aldehydes. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 1053-60. PMID 19938004 DOI: 10.1002/Chem.200901803 |
0.391 |
|
| 2010 |
Tang X, Rawson D, Woodward S. Direct Reaction of Aryl Iodideswith Activated Aluminium Powder and Reactions of the DerivedAryl Sesquiiodides Synlett. 2010: 636-638. DOI: 10.1055/S-0029-1219179 |
0.368 |
|
| 2010 |
Asikainen M, Lewis W, Blake AJ, Woodward S. An SN2′ displacement approach to allenyl acetates Tetrahedron Letters. 51: 6454-6456. DOI: 10.1016/J.Tetlet.2010.10.013 |
0.442 |
|
| 2010 |
Welker M, Woodward S. Chiral enolates for highly stereoselective aldol reactionsdScope and limitations Tetrahedron. 66: 9954-9963. DOI: 10.1016/J.Tet.2010.10.048 |
0.361 |
|
| 2010 |
Woodward S, Diéguez M, Pàmies O. Use of sugar-based ligands in selective catalysis: Recent developments Coordination Chemistry Reviews. 254: 2007-2030. DOI: 10.1016/J.Ccr.2010.03.005 |
0.619 |
|
| 2009 |
Blake AJ, Novak A, Davies M, Robinson RI, Woodward S. Preparation of 1,1′-Oxy-bis(3,3-bis(trifluoromethyl)-3(1H)-1,2-benziodoxole) and 2-(N-(p-Toluenesulfonyl)imino)iodobenzylmethyl Ether Synthetic Communications. 39: 1065-1075. DOI: 10.1080/00397910802474990 |
0.412 |
|
| 2009 |
Bertolini F, Woodward S, Crotti S, Pineschi M. A practical regioselective ring-opening of activated aziridines with organoalanes Tetrahedron Letters. 50: 4515-4518. DOI: 10.1016/J.Tetlet.2009.05.081 |
0.328 |
|
| 2009 |
Crampton RH, Hajjaji SE, Fox ME, Woodward S. Reaction prospecting by 31P NMR: enantioselective rhodium-DuPhos catalysed addition of ZnMe2 to diphenylphosphinoylimines Tetrahedron Asymmetry. 20: 2497-2503. DOI: 10.1016/J.Tetasy.2009.09.020 |
0.432 |
|
| 2009 |
Tang X, Blake AJ, Lewis W, Woodward S. Asymmetric conjugate additions to 1,1′-diactivated cyclic enones—a comparative study Tetrahedron: Asymmetry. 20: 1881-1891. DOI: 10.1016/J.Tetasy.2009.07.006 |
0.419 |
|
| 2009 |
Tang X, Woodward S, Krause N. Synthesis of α-Hydroxyallenes by Copper-Catalyzed SN2′ Substitution of Propargylic Dioxolanones European Journal of Organic Chemistry. 2009: 2836-2844. DOI: 10.1002/Ejoc.200900226 |
0.387 |
|
| 2009 |
Novak A, Calhorda MJ, Costa PJ, Woodward S. Mapping the Mechanism of Nickel-Ferrophite Catalysed Methylation of Baylis-Hillman-Derived SN2′ Electrophiles European Journal of Organic Chemistry. 2009: 898-903. DOI: 10.1002/Ejoc.200801029 |
0.397 |
|
| 2008 |
De Roma A, Ruffo F, Woodward S. Amino-sugar modular ligands-useful cores for the formation of asymmetric copper 1,4-addition catalysts. Chemical Communications (Cambridge, England). 5384-6. PMID 18985218 DOI: 10.1039/B813137F |
0.387 |
|
| 2008 |
Glynn D, Bernier D, Woodward S. Microwave acceleration in DABAL-Me3-mediated amide formation Tetrahedron Letters. 49: 5687-5688. DOI: 10.1016/J.Tetlet.2008.07.090 |
0.385 |
|
| 2008 |
Biswas K, Woodward S. Stereoselective 1,4-addition of Grignard reagents to α,β-enamides using a combined chiral auxiliary-catalyst approach Tetrahedron-Asymmetry. 19: 1702-1708. DOI: 10.1016/J.Tetasy.2008.06.017 |
0.39 |
|
| 2008 |
Meadows RE, Woodward S. Steric effects in palladium-catalysed amination of aryl triflates and nonaflates with the primary amines PhCH(R)NH2 (R=H, Me) Tetrahedron. 64: 1218-1224. DOI: 10.1016/J.Tet.2007.11.074 |
0.411 |
|
| 2008 |
Mata Y, Diéguez M, Pàmies O, Woodward S. Screening of modular sugar phosphite-oxazoline and phosphite-phosphoroamidite ligand libraries in the asymmetric nickel-catalyzed trialkylaluminium addition to aldehydes Inorganica Chimica Acta. 361: 1381-1384. DOI: 10.1016/J.Ica.2007.09.005 |
0.628 |
|
| 2007 |
Shannon J, Bernier D, Rawson D, Woodward S. Direct asymmetric catalytic 1,2-addition of RZnX to aldehydes promoted by AlMe3 and reversal of expected stereochemistry. Chemical Communications (Cambridge, England). 3945-7. PMID 17896041 DOI: 10.1039/B710681E |
0.447 |
|
| 2007 |
Blake AJ, Shannon J, Stephens JC, Woodward S. Demonstration of promoted zinc Schlenk equilibria, their equilibrium values and derived reactivity. Chemistry (Weinheim An Der Bergstrasse, Germany). 13: 2462-72. PMID 17285664 DOI: 10.1002/Chem.200601739 |
0.441 |
|
| 2007 |
Blake AJ, Giunta D, Shannon J, Solinas M, Walzer F, Woodward S. In Search of New Approaches to Asymmetric Conjugate Addition: Screening Studies on the Use of [Zn(bpy*)X(R)] Reagents and α,β-Unsaturated Amide Michael Acceptors Collection of Czechoslovak Chemical Communications. 72: 1107-1121. DOI: 10.1135/Cccc20071107 |
0.42 |
|
| 2007 |
Woodward S. Design versus Discovery in Synthetic Applications of Organoalanes Synlett. 2007: 1490-1500. DOI: 10.1055/S-2007-980376 |
0.377 |
|
| 2007 |
Diéguez M, Pàmies O, Woodward S, Mata Y. Asymmetric Ni Phosphite Catalyzed Trialkylaluminum Addition to Aldehydes Synfacts. 2007: 0078-0078. DOI: 10.1055/S-2006-955705 |
0.554 |
|
| 2007 |
Mata Y, Diéguez M, Pàmies O, Biswas K, Woodward S. Sugar–phosphite–oxazoline and phosphite–phosphoroamidite ligand libraries for Cu-catalyzed asymmetric 1,4-addition reactions Tetrahedron-Asymmetry. 18: 1613-1617. DOI: 10.1016/J.Tetasy.2007.06.024 |
0.645 |
|
| 2007 |
Mata Y, Diéguez M, Pàmies O, Woodward S. Screening of a modular sugar-based phosphite ligand library in the Cu-catalyzed asymmetric 1,4-addition reactions Journal of Organometallic Chemistry. 692: 4315-4320. DOI: 10.1016/J.Jorganchem.2007.06.063 |
0.62 |
|
| 2007 |
Novak A, Fryatt R, Woodward S. Nickel-catalysed asymmetric SN2′ substitution chemistry of Baylis–Hillman derived allylic electrophiles Comptes Rendus Chimie. 10: 206-212. DOI: 10.1016/J.Crci.2006.10.008 |
0.498 |
|
| 2007 |
Solinas M, Meadows RE, Wilson C, Blake AJ, Woodward S. Efficient Synthesis of 2-Methyl Derivatives of 1,1′-Bi(2-naphthol) and 1,1′-Bi(2-phenols) European Journal of Organic Chemistry. 2007: 1613-1623. DOI: 10.1002/Ejoc.200600962 |
0.43 |
|
| 2006 |
Mata Y, Diéguez M, Pàmies O, Woodward S. Screening of a modular sugar-based phosphite ligand library in the asymmetric nickel-catalyzed trialkylaluminum addition to aldehydes. The Journal of Organic Chemistry. 71: 8159-65. PMID 17025306 DOI: 10.1021/Jo0613535 |
0.63 |
|
| 2006 |
Biswas K, Chapron A, Cooper T, Fraser PK, Novak A, Prieto O, Woodward S. Dabbling with air-stable organoaluminum species Pure and Applied Chemistry. 78: 511-518. DOI: 10.1351/Pac200678020511 |
0.422 |
|
| 2006 |
Novak A, Humphreys LD, Walker MD, Woodward S. Amide Bond Formation Using an Air-Stable Source of AlMe3. Cheminform. 37. DOI: 10.1016/J.Tetlet.2006.06.004 |
0.357 |
|
| 2006 |
Prieto O, Woodward S. Enantioselective catalytic allylation of arylmethylketones using tetraallyltin and tin(IV) chloride mixtures Journal of Organometallic Chemistry. 691: 1515-1519. DOI: 10.1016/J.Jorganchem.2005.11.017 |
0.431 |
|
| 2006 |
Albrow V, Blake AJ, Chapron A, Wilson C, Woodward S. Preparation of planar chiral ferrocenes containing a fluorous alcohol function Inorganica Chimica Acta. 359: 1731-1742. DOI: 10.1016/J.Ica.2005.05.040 |
0.379 |
|
| 2006 |
Robinson RI, Fryatt R, Wilson C, Woodward S. Sulfonamide Ligands Attained Through Opening of Saccharin Derivatives European Journal of Organic Chemistry. 2006: 4483-4489. DOI: 10.1002/Ejoc.200600508 |
0.404 |
|
| 2006 |
Albrow VE, Blake AJ, Fryatt R, Wilson C, Woodward S. Aryl Ferrophites – A New Class of Ligands for Asymmetric Catalysis European Journal of Organic Chemistry. 2006: 2549-2557. DOI: 10.1002/Ejoc.200600071 |
0.462 |
|
| 2006 |
Cooper T, Novak A, Humphreys LD, Walker MD, Woodward S. User-friendly methylation of aryl and vinyl halides and pseudohalides with DABAL-Me3 Advanced Synthesis & Catalysis. 348: 686-690. DOI: 10.1002/Adsc.200505405 |
0.379 |
|
| 2005 |
Alexakis A, Albrow V, Biswas K, d'Augustin M, Prieto O, Woodward S. Highly enantioselective copper(I)-phosphoramidite-catalysed additions of organoaluminium reagents to enones. Chemical Communications (Cambridge, England). 2843-5. PMID 15928777 DOI: 10.1039/B503074A |
0.396 |
|
| 2005 |
Biswas K, Prieto O, Goldsmith PJ, Woodward S. Remarkably stable (Me3Al)2DABCO and stereoselective nickel-catalyzed AlR3 (R=Me, Et) additions to aldehydes. Angewandte Chemie (International Ed. in English). 44: 2232-4. PMID 15768433 DOI: 10.1002/Anie.200462569 |
0.354 |
|
| 2005 |
Biswas K, Börner C, Gimeno J, Goldsmith PJ, Ramazzotti D, So ALK, Woodward S. Expedient synthesis of β,β-disubstituted α-methylenepropionates Tetrahedron. 61: 1433-1442. DOI: 10.1016/J.Tet.2004.12.002 |
0.425 |
|
| 2005 |
Timofte RS, Titman JJ, Shao L, Stephens JC, Woodward S. Investigations into the utility of high-surface area silica pellets as potential solid-phase synthesis supports Tetrahedron. 61: 51-59. DOI: 10.1016/J.Tet.2004.10.064 |
0.319 |
|
| 2004 |
Cunningham A, Mokal-Parekh V, Wilson C, Woodward S. On the use of mixtures of organotin species for catalytic enantioselective ketone allylation--a detective story. Organic & Biomolecular Chemistry. 2: 741-8. PMID 14985815 DOI: 10.1039/B313384B |
0.42 |
|
| 2004 |
Timofte RS, Woodward S. Preparation of silane-grafted pellets: silica bound reagents in a very convenient form Tetrahedron Letters. 45: 39-42. DOI: 10.1016/J.Tetlet.2003.10.140 |
0.372 |
|
| 2004 |
Robinson RI, Stephens JC, Worden SM, Blake AJ, Wilson C, Woodward S. Sulfonic acid libraries attained through opening of 2-sulfobenzoic acid anhydride European Journal of Organic Chemistry. 4596-4605. DOI: 10.1002/Ejoc.200400562 |
0.423 |
|
| 2003 |
Fraser PK, Woodward S. Highly enantioselective conjugate addition of AlMe3 to linear aliphatic enones by a designed catalyst. Chemistry (Weinheim An Der Bergstrasse, Germany). 9: 776-83. PMID 12569471 DOI: 10.1002/Chem.200390087 |
0.406 |
|
| 2003 |
Albrow V, Biswas K, Crane A, Chaplin N, Easun T, Gladiali S, Lygo B, Woodward S. Synthesis of an octahydro-1,1′-binaphthyl thioether ligand and comparison with unhydrogenated binaphthyl analogues Tetrahedron Asymmetry. 14: 2813-2819. DOI: 10.1016/S0957-4166(03)00583-4 |
0.438 |
|
| 2003 |
Robinson RI, Woodward S. Direct formation of cyclic sulfates utilising hypervalent iodine species and sulfur trioxide adducts Tetrahedron Letters. 44: 1655-1657. DOI: 10.1016/S0040-4039(03)00039-X |
0.373 |
|
| 2002 |
Cunningham A, Woodward S. Highly Enantioselective Catalytic Ketone Allylation with Sn(CH2CH=CH2)4/RSn(CH2CH=CH2)3 Mixtures (R = Et, Bu) Synlett. 2004: 914-914. DOI: 10.1055/S-2004-820040 |
0.39 |
|
| 2002 |
Garcia-Ruiz V, Woodward S. On the absolute stereochemistry of (−)-4-alkylnonan-2-ones Tetrahedron: Asymmetry. 13: 2177-2180. DOI: 10.1016/S0957-4166(02)00574-8 |
0.397 |
|
| 2002 |
Schrader Tv, Woodward S. Highly Chemoselective Lithium Metal Reductions of Benzaldehyde Bis(2‐Methoxyethyl) Acetals European Journal of Organic Chemistry. 2002: 3833-3836. DOI: 10.1002/1099-0690(200211)2002:22<3833::Aid-Ejoc3833>3.0.Co;2-K |
0.408 |
|
| 2001 |
Fraser PK, Woodward S. Strong ligand accelerated catalysis by an Arduengo-type carbene in copper-catalysed conjugate addition Tetrahedron Letters. 42: 2747-2749. DOI: 10.1016/S0040-4039(01)00280-5 |
0.433 |
|
| 2001 |
Börner C, König WA, Woodward S. Enone structure as a probe to Lewis acid carbonyl binding in copper-catalysed asymmetric conjugate addition Tetrahedron Letters. 42: 327-329. DOI: 10.1016/S0040-4039(00)01940-7 |
0.355 |
|
| 2001 |
Börner C, Dennis M, Sinn E, Woodward S. Copper-Catalysed Asymmetric 1,4-Addition of Organozinc Compounds to Linear Aliphatic Enones Using 2,2′-Dihydroxy 3,3′-Dithioether Derivatives of 1,1′-Binaphthalene European Journal of Organic Chemistry. 2001: 2435-2446. DOI: 10.1002/1099-0690(200107)2001:13<2435::Aid-Ejoc2435>3.0.Co;2-0 |
0.465 |
|
| 2000 |
Blake AJ, Cunningham A, Ford A, Teat SJ, Woodward S. Enantioselective reduction of prochiral ketones by catecholborane catalysed by chiral group 13 complexes Chemistry (Weinheim An Der Bergstrasse, Germany). 6: 3586-94. PMID 11072824 DOI: 10.1002/1521-3765(20001002)6:19<3586::Aid-Chem3586>3.0.Co;2-S |
0.405 |
|
| 2000 |
Börner C, Gimeno J, Gladiali S, Goldsmith PJ, Ramazzotti D, Woodward S. Asymmetric chemo- and regiospecific addition of organozinc reagents to Baylis–Hillman derived allylic electrophiles Chemical Communications. 2433-2434. DOI: 10.1039/B006943O |
0.5 |
|
| 2000 |
Cunningham A, Dennis MR, Woodward S. Efficient routes to alkyl ether linked derivatives of 1,1′-(bi-2-naphthol) bearing 3-N,N-dialkylamide substituents Journal of the Chemical Society-Perkin Transactions 1. 4422-4426. DOI: 10.1039/B005701K |
0.317 |
|
| 2000 |
Woodward S. Decoding the ‘black box’ reactivity that is organocuprate conjugate addition chemistry Chemical Society Reviews. 29: 393-401. DOI: 10.1039/B002690P |
0.324 |
|
| 2000 |
Chipperfield JR, Clayton J, Khan SA, Woodward S. Combined visible spectroscopy-conductance-electrospray mass spectrometry studies of paramagnetic catalysts. Speciation of Jacobsen's manganese salen complex † in the presence of σ-donor ligands, hydroxide sources, and cumyl hydroperoxide‡ Journal of the Chemical Society, Dalton Transactions. 1087-1094. DOI: 10.1039/B001059F |
0.351 |
|
| 2000 |
Pàmies O, Net G, Ruiz A, Claver C, Woodward S. Copper-catalysed asymmetric conjugate addition of organometallic reagents to enones using S,O-ligands with a xylofuranose backbone Tetrahedron: Asymmetry. 11: 871-877. DOI: 10.1016/S0957-4166(99)00546-7 |
0.36 |
|
| 2000 |
Bennett SMW, Brown SM, Cunningham A, Dennis MR, Muxworthy JP, Oakley MA, Woodward S. Copper-Catalysed Asymmetric Conjugate Addition of Organometallic Reagents to Linear Enones Tetrahedron. 56: 2847-2855. DOI: 10.1016/S0040-4020(00)00140-X |
0.379 |
|
| 1999 |
Ford A, Woodward S. Catalytic Enantioselective Reduction of Ketones by a Chiral Gallium Complex and Catecholborane. Angewandte Chemie (International Ed. in English). 38: 335-336. PMID 29711655 DOI: 10.1002/(Sici)1521-3773(19990201)38:3<335::Aid-Anie335>3.0.Co;2-T |
0.418 |
|
| 1999 |
Ford A, Woodward S. Enantioselective Reduction of Ketones by in situ Generated Borane and Cbs Catalyst: Economical Alternative to Bh3-Thf Synthetic Communications. 29: 189-192. DOI: 10.1080/00397919908085756 |
0.377 |
|
| 1999 |
Bennett SMW, Brown SM, Conole G, Dennis MR, Fraser PK, Radojevic S, McPartlin M, Topping CM, Woodward S. Catalytic conjugate addition promoted by the copper(I)-monothiobinaphthol system. Part 3. Comparison of three thiolate-based catalytic systems Journal of the Chemical Society-Perkin Transactions 1. 3127-3132. DOI: 10.1039/A906373K |
0.417 |
|
| 1999 |
Oakley MA, Woodward S, Coupland K, Parker D, Temple-Heald C. Practical dihydroxylation and C–C cleavage of unsaturated fatty acids Journal of Molecular Catalysis a: Chemical. 150: 105-111. DOI: 10.1016/S1381-1169(99)00213-7 |
0.335 |
|
| 1999 |
Blackmore IJ, Boa AN, Murray EJ, Dennis M, Woodward S. A simple preparation of iodoarenes, iodoalkenes and iodoalkynes by reaction of organolithiums with 2,2,2-trifluoro-1-iodoethane Tetrahedron Letters. 40: 6671-6672. DOI: 10.1016/S0040-4039(99)01343-X |
0.363 |
|
| 1999 |
Bennett SM, Brown SM, Muxworthy JP, Woodward S. Copper-catalysed asymmetric conjugate addition of organometallic reagents to linear enones using thiourethane ligands Tetrahedron Letters. 40: 1767-1770. DOI: 10.1016/S0040-4039(98)02686-0 |
0.412 |
|
| 1998 |
Dennis MR, Woodward S. Enantiopure 3-amido or 3,3′-bisamido substituted 1,1′-bi-2-naphthols by anionic Fries rearrangements Journal of the Chemical Society-Perkin Transactions 1. 1081-1086. DOI: 10.1039/A708436F |
0.401 |
|
| 1997 |
Ford AR, Sinn E, Woodward S. Exploitation of Differential Reactivity of the Carbon-Chlorine Bonds in 1,3-Dichloroisoquinoline. Routes to New N,N-Chelate Ligands and 1,3- Disubstituted Isoquinolines. Journal of the Chemical Society-Perkin Transactions 1. 927-934. DOI: 10.1039/A605827B |
0.411 |
|
| 1997 |
Azad SM, Bennett SMW, Brown SM, Green J, Sinn E, Topping CM, Woodward S. Catalytic conjugate addition promoted by the copper(I)–monothiobinaphthol system. Part 2.1 Optimal ligand synthesis and initial catalytic results Journal of the Chemical Society-Perkin Transactions 1. 687-694. DOI: 10.1039/A605620B |
0.451 |
|
| 1997 |
Rhodes B, Rowling S, Tidswell P, Woodward S, Brown SM. Aerobic epoxidation via alkyl-2-oxocyclopentanecarboxylate co-oxidation with cobalt or manganese Jacobsen-type catalysts Journal of Molecular Catalysis a-Chemical. 116: 375-384. DOI: 10.1016/S1381-1169(96)00360-3 |
0.362 |
|
| 1995 |
Green J, Woodward S. Selective Monoacylation of 2,2’-Binaphthol as a Route to New Monothiobinaphthol-based Copper Catalysts for Conjugate Addition Synlett. 1995: 155-156. DOI: 10.1055/S-1995-4891 |
0.324 |
|
| 1995 |
Backhouse JR, Lowe HM, Sinn E, Suzuki S, Woodward S. Bromination of Molybdenum Carbonyls Revisited: Oxo Complexes and Routes to New Materials Chemistry Journal of the Chemical Society-Dalton Transactions. 1489-1495. DOI: 10.1039/Dt9950001489 |
0.407 |
|
| 1995 |
Bennett S, Brown SM, Conole G, Kessler M, Rowling S, Sinn E, Woodward S. Structure and Mechanism in Aerobic Alkene Epoxidations Promoted by Ruthenium Complexes of Bis(dihydrooxazole) Ligands Journal of the Chemical Society-Dalton Transactions. 367-376. DOI: 10.1039/Dt9950000367 |
0.414 |
|
| 1995 |
Ford AR, Sinn E, Woodward S. Regioselectivity in metallation reactions of 2-(2′-naphthyl)pyridine: 1′-versus 3′-reactivity in mercuration and palladation reactions. Crystal structure of chloro(pyridine) [2-(2−pyridiny)naphthyl-C3,N]palladium Journal of Organometallic Chemistry. 493: 215-220. DOI: 10.1016/0022-328X(94)05367-K |
0.391 |
|
| 1995 |
Green J, Sinn E, Woodward S. Convenient preparation of [CuX(PCy3)2](X = Br, I, SCN, N3) complexes. X-ray crystal structure of [Cu(N3)(PCy3)2] (Cy = cyclo-C6H11) Inorganica Chimica Acta. 230: 231-233. DOI: 10.1016/0020-1693(94)04296-8 |
0.324 |
|
| 1994 |
Chipperfield JR, Woodward S. Reliable and Economical Preparation of Macrocyclic Complexes: Synthesis and Reactivity of a Tetraazaligand for an Advanced Inorganic Laboratory Journal of Chemical Education. 71: 75. DOI: 10.1021/Ed071P75 |
0.325 |
|
| 1994 |
Ford A, Sinn E, Woodward S. Preparation of dimolybdenum cations with triply bridged cores [Mo2(μ-F)2(μ-X)(CO)4(PPh3 )4]+ (X F, Cl, Br, OH),.. Polyhedron. 13: 635-645. DOI: 10.1016/S0277-5387(00)84740-3 |
0.313 |
|
| 1993 |
Green J, Sinn E, Woodward S, Butcher R. Mechanistic insights into catalytic cyclopropanation by copper(I) phosphine complexes. X-ray crystal structures of [Cu(FBF3)(PCy3)2] (Cy = cyclo-C6H11) and [Cu(MeCN)2{1,2-C6H4CH2NMe2(PPh2)}]BF4 Polyhedron. 12: 991-1001. DOI: 10.1016/S0277-5387(00)87175-2 |
0.335 |
|
| 1991 |
Adams H, Bailey NA, Gauntlett JT, Winter MJ, Woodward S. Synthesis and X-ray crystal structure of the dimolybdenum acetaldehyde complex [Mo2(η-MeCHO)(CO)4(η-C5H 5)2] Journal of the Chemical Society, Dalton Transactions. 2217-2221. DOI: 10.1039/Dt9910002217 |
0.647 |
|
| 1991 |
Gauntlett JT, Mann BE, Winter MJ, Woodward S. Reaction of [WMe(CO)3(η-C5H5)] with LiBHEt3. Formation and reactions of the anionic formyl trans-[W(CHO)Me(CO)2(η-C5H5)]− and the anionic hydrido acyl trans-[WH(COMe)(CO)2(η-C5H5)]− Journal of the Chemical Society-Dalton Transactions. 1427-1432. DOI: 10.1039/Dt9910001427 |
0.632 |
|
| 1991 |
Adams H, Bailey NA, Gauntlett JT, Harkin IM, Winter MJ, Woodward S. Formation of the alkoxyalkyl complexes [m{CHMe(OMe)}(CO)2(η-C5H4R)] (M = Mo, R = H; M = W, R = H or Me) and their transformations by loss of MeOH into η3-propenoyl or vinyl complexes. Crystal structures of [Mo{CHMe(PPh3)}(CO)2(PPh3)(η-C 5H5)]BF4.. Journal of the Chemical Society, Dalton Transactions. 1117-1128. DOI: 10.1039/Dt9910001117 |
0.651 |
|
| 1991 |
Adams H, Bailey NA, Winter MJ, Woodward S. Hydride to carbene migration in the CpMH{C(OEt)Ph}(CO)2 (M = Mo, W) system and subsequent rearrangement of the consequent products to η3-benzyl complexes. X-Ray crystal structure of the η3-benzyl CpW(CO)2{η3-C6H5CH(OEt)} Journal of Organometallic Chemistry. 418: C39-C42. DOI: 10.1016/0022-328X(91)80230-H |
0.62 |
|
| 1991 |
Adams H, Bailey NA, Winter MJ, Woodward S. Hydride to carbene migration in the CpMH{=C(NHEt)Ph}(CO)2 (M = Mo, W) system. X-Ray crystal structure of CpMo η2-CH(Ph)NHEt (CO)2 Journal of Organometallic Chemistry. 410: C21-C24. DOI: 10.1016/0022-328X(91)80013-A |
0.611 |
|
| 1990 |
Woodward S, Riaz U, Curtis MD, Haggerty BS, Rheingold AL. Cyclopentadienylniobium and -molybdenum phosphorodithioate complexes. X-ray crystal structures of CpNbCl3[S2P(OPr-iso)2], CpNbCl(.mu.-Cl)2Nb[S2P(OPr-iso)2]Cp, and cis-Cp'Mo(CO)2[S2P(OPr-iso)2] Organometallics. 9: 2703-2708. DOI: 10.1021/Om00160A017 |
0.333 |
|
| 1989 |
Winter MJ, Woodward S. Synthesis of molybdenum and tungsten nonheteroatom stabilised carbene complexes M(SnPh3)(CO)2(CPhR)(η-C5H5)(M = Mo, W; R = H, Me); and an example of triphenyltin to nonheteroatom stabilised carbene migration Journal of the Chemical Society, Chemical Communications. 457-458. DOI: 10.1039/C39890000457 |
0.626 |
|
| 1989 |
Bentley GW, Hough G, Winter MJ, Woodward S. Synthesis and reactions of LM(SnPh3)(CO)2{C(OEt)Ph} (L = C5Me5 or η5-C9H7; M = Mo or W) Polyhedron. 8: 1861-1862. DOI: 10.1016/S0277-5387(00)80674-9 |
0.637 |
|
| 1989 |
Ridgway C, Winter MJ, Woodward S. Vinyl to carbonyl migration at molybdenum Polyhedron. 8: 1859-1860. DOI: 10.1016/S0277-5387(00)80673-7 |
0.597 |
|
| 1989 |
Winter MJ, Woodward S. Synthesis and reactions of the tungsten nonheteroatom-stabilised carbene anion [CpW(CO)2(CHPh)]− Journal of Organometallic Chemistry. 361. DOI: 10.1016/0022-328X(89)87365-6 |
0.614 |
|
| 1988 |
Bailey NA, Dunn DA, Foxcroft CN, Harrison GR, Winter MJ, Woodward S. Pentamethylcyclopentadienyl molybdenum and tungsten carbene complexes. X-Ray crystal structures of cis- and trans-[Mol(CO)2{=C(CH2)3O}(η-C 5Me5)] Journal of the Chemical Society, Dalton Transactions. 1449-1456. DOI: 10.1039/Dt9880001449 |
0.638 |
|
| 1988 |
Trevor Gauntlett J, Mann BE, Winter MJ, Woodward S. The reaction of CpWMe(CO)3 with LiEt3BH. Formation of the formyl complex trans-[CpWMe(CHO)(CO)2]− and the (hydrido)(acyl) complex trans-[CpWH(COMe)(CO)2]− Journal of Organometallic Chemistry. 342: C5-C9. DOI: 10.1016/0022-328X(88)80052-4 |
0.616 |
|
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