| Year |
Citation |
Score |
| 2019 |
Gorman RM, Hurst TE, Petersen WF, Taylor RJ. A copper(II)-mediated radical cross-dehydrogenative coupling/sulfinic acid elimination approach to 2-quinolones Tetrahedron. 75: 130711. DOI: 10.1016/J.Tet.2019.130711 |
0.301 |
|
| 2018 |
Hurst TE, Gorman R, Drouhin P, Taylor RJ. Application of copper(II)-mediated radical cross-dehydrogenative coupling to prepare spirocyclic oxindoles and to a formal total synthesis of Satavaptan Tetrahedron. 74: 6485-6496. DOI: 10.1016/J.Tet.2018.09.026 |
0.319 |
|
| 2017 |
Petersen WF, Taylor RJ, Donald JR. Photoredox-Catalyzed Reductive Carbamoyl Radical Generation: A Redox-Neutral Intermolecular Addition-Cyclization Approach to Functionalized 3,4-Dihydroquinolin-2-ones. Organic Letters. PMID 28135099 DOI: 10.1021/Acs.Orglett.7B00022 |
0.311 |
|
| 2016 |
James MJ, Grant ND, O'Brien P, Taylor RJ, Unsworth WP. Catalytic Dearomatization Approach to Quinolizidine Alkaloids: Five Step Total Synthesis of (±)-Lasubine II. Organic Letters. 18: 6256-6259. PMID 27978692 DOI: 10.1021/Acs.Orglett.6B03017 |
0.34 |
|
| 2016 |
Liddon JT, Clarke AK, Taylor RJ, Unsworth WP. Preparation and Reactions of Indoleninyl Halides: Scaffolds for the Synthesis of Spirocyclic Indole Derivatives. Organic Letters. 18: 6328-6331. PMID 27978677 DOI: 10.1021/Acs.Orglett.6B03221 |
0.319 |
|
| 2016 |
Clarke AK, Liddon JT, Cuthbertson JD, Taylor RJ, Unsworth WP. Dearomatisation approaches to spirocyclic dienones via the electrophilic activation of alkynes. Organic & Biomolecular Chemistry. PMID 27901167 DOI: 10.1039/C6Ob02426B |
0.767 |
|
| 2016 |
Ronson TO, Kitsiou C, Unsworth WP, Taylor RJ. Synthetic approaches to pallimamine and analogues using direct imine acylation Tetrahedron. 72: 6099-6106. DOI: 10.1016/J.Tet.2016.05.009 |
0.334 |
|
| 2015 |
James MJ, O'Brien P, Taylor RJ, Unsworth WP. Synthesis of Spirocyclic Indolenines. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26661053 DOI: 10.1002/Chem.201503835 |
0.315 |
|
| 2015 |
Ronson TO, Burns MJ, Voelkel MH, Evans KJ, Lynam JM, Taylor RJ, Fairlamb IJ. Total Synthesis and Stereochemical Revision of Phacelocarpus 2-Pyrone A. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26568186 DOI: 10.1002/Chem.201504089 |
0.31 |
|
| 2015 |
James MJ, Clubley RE, Palate KY, Procter TJ, Wyton AC, O'Brien P, Taylor RJ, Unsworth WP. Silver(I)-Catalyzed Dearomatization of Alkyne-Tethered Indoles: Divergent Synthesis of Spirocyclic Indolenines and Carbazoles. Organic Letters. 17: 4372-5. PMID 26293968 DOI: 10.1021/Acs.Orglett.5B02216 |
0.324 |
|
| 2015 |
James MJ, Cuthbertson JD, O'Brien P, Taylor RJ, Unsworth WP. Silver(I)- or Copper(II)-Mediated Dearomatization of Aromatic Ynones: Direct Access to Spirocyclic Scaffolds. Angewandte Chemie (International Ed. in English). 54: 7640-3. PMID 25960013 DOI: 10.1002/Anie.201501812 |
0.765 |
|
| 2015 |
Drouhin P, Hurst TE, Whitwood AC, Taylor RJ. Substrate scope in the copper-mediated construction of bis-oxindoles via a double C–H/Ar–H coupling process Tetrahedron. 71: 7124-7136. DOI: 10.1016/J.Tet.2015.02.060 |
0.319 |
|
| 2015 |
Ronson TO, Taylor RJ, Fairlamb IJ. Palladium-catalysed macrocyclisations in the total synthesis of natural products Tetrahedron. 71: 989-1009. DOI: 10.1016/J.Tet.2014.11.009 |
0.31 |
|
| 2015 |
Lloyd MG, D'Acunto M, Taylor RJ, Unsworth WP. α-Alkylidene-γ-butyrolactone synthesis via one-pot C–H insertion/olefination: substrate scope and the total synthesis of (±)-cedarmycins A and B Tetrahedron. 71: 7107-7123. DOI: 10.1016/J.Tet.2014.09.054 |
0.322 |
|
| 2014 |
Burns MJ, Ronson TO, Taylor RJ, Fairlamb IJ. 4-Hydroxy-6-alkyl-2-pyrones as nucleophilic coupling partners in Mitsunobu reactions and oxa-Michael additions. Beilstein Journal of Organic Chemistry. 10: 1159-65. PMID 24991267 DOI: 10.3762/Bjoc.10.116 |
0.306 |
|
| 2013 |
Unsworth WP, Taylor RJ. 'Upenamide: trials and tribulations. Organic & Biomolecular Chemistry. 11: 7250-61. PMID 24057754 DOI: 10.1039/C3Ob41519H |
0.303 |
|
| 2013 |
Unsworth WP, Kitsiou C, Taylor RJ. An expedient protecting-group-free total synthesis of (±)-dievodiamine. Organic Letters. 15: 3302-5. PMID 23786450 DOI: 10.1021/Ol4013469 |
0.342 |
|
| 2013 |
Unsworth WP, Cuthbertson JD, Taylor RJ. Total synthesis of spirobacillene A. Organic Letters. 15: 3306-9. PMID 23786419 DOI: 10.1021/Ol4013958 |
0.778 |
|
| 2013 |
Burns DJ, Mommer S, O'Brien P, Taylor RJ, Whitwood AC, Hachisu S. Stereocontrolled synthesis of the AB rings of samaderine C. Organic Letters. 15: 394-7. PMID 23302065 DOI: 10.1021/Ol303385A |
0.325 |
|
| 2013 |
Unsworth WP, Gallagher KA, Jean M, Schmidt JP, Diorazio LJ, Taylor RJ. Direct imine acylation: synthesis of the proposed structures of 'upenamide. Organic Letters. 15: 262-5. PMID 23265326 DOI: 10.1021/Ol3030764 |
0.332 |
|
| 2013 |
Unsworth WP, Kitsiou C, Taylor RJ. Direct imine acylation: rapid access to diverse heterocyclic scaffolds. Organic Letters. 15: 258-61. PMID 23265307 DOI: 10.1021/Ol303073B |
0.302 |
|
| 2013 |
Cuthbertson JD, Taylor RJ. A telescoped route to 2,6-disubstituted 2,3,4,5-tetrahydropyridines and 2,6-syn-disubstituted piperidines: total synthesis of (-)-grandisine G. Angewandte Chemie (International Ed. in English). 52: 1490-3. PMID 23239287 DOI: 10.1002/Anie.201208118 |
0.765 |
|
| 2012 |
Burns DJ, Hachisu S, O'Brien P, Taylor RJ. Catalytic asymmetric synthesis of butane diacetal-protected (4S,5S)-dihydroxycyclohexen-1-one and use in natural product synthesis. Organic & Biomolecular Chemistry. 10: 7666-8. PMID 22930235 DOI: 10.1039/C2Ob26406D |
0.325 |
|
| 2012 |
Doveston RG, Steendam R, Jones S, Taylor RJ. Total synthesis of an oxepine natural product, (±)-janoxepin. Organic Letters. 14: 1122-5. PMID 22288766 DOI: 10.1021/Ol300039X |
0.745 |
|
| 2012 |
Craven PG, Taylor RJ. Total synthesis and structural confirmation of (±)-cuevaene A Tetrahedron Letters. 53: 5422-5425. DOI: 10.1016/J.Tetlet.2012.07.121 |
0.314 |
|
| 2012 |
Doveston RG, Taylor RJ. An expedient synthesis of the proposed biosynthetic precursor of the oxepine natural product, janoxepin Tetrahedron Letters. 53: 2533-2536. DOI: 10.1016/J.Tetlet.2012.03.025 |
0.325 |
|
| 2011 |
Franckevičius V, Cuthbertson JD, Pickworth M, Pugh DS, Taylor RJ. Asymmetric decarboxylative allylation of oxindoles. Organic Letters. 13: 4264-7. PMID 21776973 DOI: 10.1055/S-0030-1261132 |
0.773 |
|
| 2011 |
Cuthbertson JD, Godfrey AA, Taylor RJ. The preparation of (-)-grandisine B from (+)-grandisine D; a biomimetic total synthesis or formation of an isolation artefact? Organic Letters. 13: 3976-9. PMID 21718048 DOI: 10.1021/Ol2014939 |
0.769 |
|
| 2011 |
Kitson RR, McAllister GD, Taylor RJ. Synthesis of yomogin using a telescoped α-methylene-γ-butyrolactone annelation procedure Tetrahedron Letters. 52: 561-564. DOI: 10.1016/J.Tetlet.2010.11.143 |
0.751 |
|
| 2010 |
Burns AR, McAllister GD, Shanahan SE, Taylor RJ. Total synthesis and structural reassignment of (+)-dictyosphaeric acid A: a tandem intramolecular Michael addition/alkene migration approach. Angewandte Chemie (International Ed. in English). 49: 5574-7. PMID 20583023 DOI: 10.1002/Anie.201002416 |
0.313 |
|
| 2010 |
Sehnal P, Taylor RJ, Fairlamb IJ. Emergence of palladium(IV) chemistry in synthesis and catalysis. Chemical Reviews. 110: 824-89. PMID 20143876 DOI: 10.1021/Cr9003242 |
0.324 |
|
| 2010 |
Kapdi AR, Taylor RJ, Fairlamb IJ. Highly regio- and chemoselective palladium(0)-mediated allylic substitution of difunctional allylic halides with phenols Tetrahedron Letters. 51: 6378-6380. DOI: 10.1016/J.Tetlet.2010.09.125 |
0.339 |
|
| 2010 |
Lubkoll J, Millemaggi A, Perry A, Taylor RJ. Tandem Horner–Wadsworth–Emmons/Heck procedures for the preparation of 3-alkenyl-oxindoles: the synthesis of Semaxanib and GW441756 Tetrahedron. 66: 6606-6612. DOI: 10.1016/J.Tet.2010.03.018 |
0.337 |
|
| 2009 |
Kitson RR, Millemaggi A, Taylor RJ. The renaissance of alpha-methylene-gamma-butyrolactones: new synthetic approaches. Angewandte Chemie (International Ed. in English). 48: 9426-51. PMID 19938025 DOI: 10.1002/Anie.200903108 |
0.723 |
|
| 2009 |
Kitson RR, Taylor RJ, Wood JL. A one-pot, base-free annelation approach to alpha-alkylidene-gamma-butyrolactones. Organic Letters. 11: 5338-41. PMID 19860387 DOI: 10.1021/Ol902191D |
0.726 |
|
| 2009 |
Catozzi N, Edwards MG, Raw SA, Wasnaire P, Taylor RJ. Synthesis of the louisianin alkaloid family via a 1,2,4-triazine inverse-electron-demand Diels-Alder approach. The Journal of Organic Chemistry. 74: 8343-54. PMID 19780559 DOI: 10.1021/Jo901761R |
0.519 |
|
| 2009 |
Edwards MG, Pugh DS, Whitwood AC, Taylor RJ. gem-Dimethylcyclopropanation of dibenzylideneacetone using triisopropyl sulfoxonium tetrafluoroborate. Acta Crystallographica. Section C, Crystal Structure Communications. 65: o39-41. PMID 19190384 DOI: 10.1107/S0108270108042431 |
0.502 |
|
| 2009 |
Kitson R, Millemaggi A, Taylor R. Die Renaissance der α-Methylen-γ-butyrolactone: neue Syntheseansätze Angewandte Chemie. 121: 9590-9615. DOI: 10.1002/Ange.200903108 |
0.711 |
|
| 2008 |
Edwards MG, Kenworthy MN, Kitson RR, Scott MS, Taylor RJ. The telescoped intramolecular michael/olefination (TIMO) approach to alpha-alkylidene-gamma-butyrolactones: synthesis of (+)-paeonilactone B. Angewandte Chemie (International Ed. in English). 47: 1935-7. PMID 18228235 DOI: 10.1002/Anie.200705329 |
0.77 |
|
| 2008 |
Barfoot CW, Burns AR, Edwards MG, Kenworthy MN, Ahmed M, Shanahan SE, Taylor RJ. A convergent synthesis of the tricyclic core of the dictyosphaeric acids. Organic Letters. 10: 353-6. PMID 18095699 DOI: 10.1021/Ol702887E |
0.538 |
|
| 2008 |
Taylor R, Edwards M, Kenworthy M, Kitson R, Scott M. Synthesis of (+)-Paeonilactone B Synfacts. 2008: 0675-0675. DOI: 10.1055/S-2008-1077860 |
0.767 |
|
| 2008 |
Catozzi N, Wasnaire P, Taylor RJ. An efficient 1,2,4-triazine-based route to the louisianin alkaloids Tetrahedron Letters. 49: 2865-2868. DOI: 10.1016/J.Tetlet.2008.03.026 |
0.31 |
|
| 2008 |
Webb MR, Addie MS, Crawforth CM, Dale JW, Franci X, Pizzonero M, Donald C, Taylor RJ. The syntheses of rac-inthomycin A, (+)-inthomycin B and (+)-inthomycin C using a unified synthetic approach Tetrahedron. 64: 4778-4791. DOI: 10.1016/J.Tet.2008.01.116 |
0.338 |
|
| 2007 |
Schmidt JP, Beltrán-Rodil S, Cox RJ, McAllister GD, Reid M, Taylor RJ. The first synthesis of the ABC-ring system of 'upenamide. Organic Letters. 9: 4041-4. PMID 17764195 DOI: 10.1021/Ol701772D |
0.328 |
|
| 2007 |
Taylor R, Catozzi N, Bromley W, Wasnaire P, Gibson M. Improved and Practical Procedures for the Preparation of Highly Substituted Pyridines and Pyridazines via Silica-Mediated Aromatisation Synlett. 2007: 2217-2221. DOI: 10.1055/S-2007-984918 |
0.319 |
|
| 2007 |
Donald JR, Edwards MG, Taylor RJ. Tandem oxime formation—epoxide ring opening sequences for the preparation of oxazines related to the trichodermamides Tetrahedron Letters. 48: 5201-5204. DOI: 10.1016/J.Tetlet.2007.05.145 |
0.536 |
|
| 2007 |
Bromley WJ, Gibson M, Lang S, Raw SA, Whitwood AC, Taylor RJ. Tandem inverse electron demand Diels–Alder, retro-Diels–Alder and intramolecular Diels–Alder sequences: one-pot synthesis of diaza-polycycles Tetrahedron. 63: 6004-6014. DOI: 10.1016/J.Tet.2007.02.056 |
0.333 |
|
| 2006 |
Taylor RJ, McAllister GD, Franck RW. The Ramberg-Bäcklund reaction for the synthesis of C-glycosides, C-linked-disaccharides and related compounds. Carbohydrate Research. 341: 1298-311. PMID 16631146 DOI: 10.1016/J.Carres.2006.03.013 |
0.307 |
|
| 2006 |
Khorphueng P, Tummatorn J, Petsom A, Taylor RJ, Roengsumran S. Total synthesis of 6-deoxyclitoriacetal isolated from Stemona collinsae Craib. Tetrahedron Letters. 47: 5989-5991. DOI: 10.1016/J.Tetlet.2006.05.188 |
0.342 |
|
| 2006 |
Webb MR, Donald C, Taylor RJ. A general route to the Streptomyces-derived inthomycin family: the first synthesis of (+)-inthomycin B Tetrahedron Letters. 47: 549-552. DOI: 10.1016/J.Tetlet.2005.11.042 |
0.335 |
|
| 2005 |
Fernández Sainz Y, Raw SA, Taylor RJ. Improved methodologies for the preparation of highly substituted pyridines. The Journal of Organic Chemistry. 70: 10086-95. PMID 16292844 DOI: 10.1021/Jo0518304 |
0.332 |
|
| 2005 |
Krebs O, Taylor RJ. Synthesis of the eastern portion of ajudazol a based on Stille coupling and double acetylene carbocupration. Organic Letters. 7: 1063-6. PMID 15760139 DOI: 10.1021/Ol047313+ |
0.323 |
|
| 2005 |
Foot JS, Giblin GM, Whitwood AC, Taylor RJ. Unexpected Z-stereoselectivity in the Ramberg-Bäcklund reaction of diarylsulfones leading to cis-stilbenes: the effect of aryl substituents and application in the synthesis of the integrastatin nucleus. Organic & Biomolecular Chemistry. 3: 756-63. PMID 15731861 DOI: 10.1039/B418426B |
0.304 |
|
| 2005 |
Bundu A, Berry NG, Gill CD, Dwyer CL, Stachulski AV, Taylor RJ, Whittall J. The design and synthesis of novel anomeric hydroperoxides: influence of the carbohydrate residue in the enantioselective epoxidation of quinones Tetrahedron: Asymmetry. 16: 283-293. DOI: 10.1016/J.Tetasy.2004.11.015 |
0.316 |
|
| 2004 |
Raw SA, Taylor RJ. Cascade reactions of substituted 1,2,4-triazines: rapid access to nitrogen-containing polycycles. Journal of the American Chemical Society. 126: 12260-1. PMID 15453747 DOI: 10.1021/Ja045780G |
0.305 |
|
| 2004 |
Raw SA, Taylor RJ. Highly substituted pyridines via tethered imine-enamine (TIE) methodology. Chemical Communications (Cambridge, England). 508-9. PMID 14973581 DOI: 10.1039/B316107B |
0.308 |
|
| 2004 |
Reid M, Taylor RJ. A stannous chloride-induced deacetalisation–cyclisation process to prepare the ABC ring system of 'upenamide Tetrahedron Letters. 45: 4181-4183. DOI: 10.1016/J.Tetlet.2004.03.119 |
0.3 |
|
| 2004 |
Martina SL, Taylor RJ. New solid-supported phosphonate reagents for the synthesis of Z-α,β-unsaturated esters Tetrahedron Letters. 45: 3279-3282. DOI: 10.1016/J.Tetlet.2004.02.138 |
0.302 |
|
| 2004 |
McAllister GD, Taylor RJ. An improved synthesis of the scyphostatin side-chain Tetrahedron Letters. 45: 2551-2554. DOI: 10.1016/J.Tetlet.2004.01.156 |
0.327 |
|
| 2004 |
Harvey JE, Kenworthy MN, Taylor RJ. Synthesis of non-proteinogenic phenylalanine analogues by Suzuki cross-coupling of a serine-derived alkyl boronic acid Tetrahedron Letters. 45: 2467-2471. DOI: 10.1016/J.Tetlet.2003.12.154 |
0.307 |
|
| 2004 |
Chaignon NM, Fairlamb IJ, Kapdi AR, Taylor RJ, Whitwood AC. Bis(triphenylphosphine)palladium(II)phthalimide – an easily prepared precatalyst for efficient Suzuki–Miyaura coupling of aryl bromides Journal of Molecular Catalysis a: Chemical. 219: 191-199. DOI: 10.1016/J.Molcata.2004.05.008 |
0.306 |
|
| 2003 |
Foot JS, Giblin GM, Taylor RJ. Synthesis of the integrastatin nucleus using the Ramberg-Bäcklund reaction. Organic Letters. 5: 4441-4. PMID 14602020 DOI: 10.1021/Ol035786V |
0.32 |
|
| 2003 |
Lewis A, Stefanuti I, Swain SA, Smith SA, Taylor RJ. A formal total synthesis of (+)-apicularen A: base-induced conversion of apicularen-derived intermediates into salicylihalamide-like products. Organic & Biomolecular Chemistry. 1: 104-16. PMID 12929396 DOI: 10.1039/B209637B |
0.348 |
|
| 2003 |
Murray LM, O'Brien P, Taylor RJ. Stereoselective reactions of a (-)-quinic acid-derived enone: application to the synthesis of the core of scyphostatin. Organic Letters. 5: 1943-6. PMID 12762692 DOI: 10.1021/Ol034521D |
0.319 |
|
| 2003 |
Murphy PV, McDonnell C, Hämig L, Paterson DE, Taylor RJ. Confirmation of the structure of a glucono-1,4-lactone derivative obtained from silylation of glucono-1,5-lactone Tetrahedron: Asymmetry. 14: 79-85. DOI: 10.1016/S0957-4166(02)00747-4 |
0.53 |
|
| 2002 |
Collier PN, Campbell AD, Patel I, Raynham TM, Taylor RJ. Enantiomerically pure alpha-amino acid synthesis via hydroboration-suzuki cross-coupling. The Journal of Organic Chemistry. 67: 1802-15. PMID 11895396 DOI: 10.1021/Jo010865A |
0.314 |
|
| 2002 |
Runcie KA, Taylor RJ. A short and efficient route to novel scyphostatin analogues. Organic Letters. 3: 3237-9. PMID 11594803 DOI: 10.1021/Ol0164132 |
0.342 |
|
| 2002 |
Collier PN, Patel I, Taylor RJ. Heck reactions of amino acid building blocks: application to the synthesis of pyrrololine analogues Tetrahedron Letters. 43: 3401-3405. DOI: 10.1016/S0040-4039(02)00512-9 |
0.303 |
|
| 2002 |
Collier PN, Campbell AD, Patel I, Taylor RJ. Hydroboration–Suzuki cross coupling of unsaturated amino acids; the synthesis of pyrimine derivatives Tetrahedron. 58: 6117-6125. DOI: 10.1016/S0040-4020(02)00541-0 |
0.311 |
|
| 2002 |
Paterson D, Griffin F, Alcaraz M, Taylor R. A Ramberg−Bäcklund Approach to the Synthesis ofC-Glycosides,C-Linked Disaccharides, andC-Glycosyl Amino Acids European Journal of Organic Chemistry. 2002: 1323-1336. DOI: 10.1002/1099-0690(200204)2002:7<1323::Aid-Ejoc1323>3.0.Co;2-8 |
0.316 |
|
| 2002 |
Griffin F, Paterson D, Murphy P, Taylor R. A New Route toexo-Glycals Using the Ramberg−Bäcklund Rearrangement European Journal of Organic Chemistry. 2002: 1305-1322. DOI: 10.1002/1099-0690(200204)2002:7<1305::Aid-Ejoc1305>3.0.Co;2-0 |
0.492 |
|
| 2001 |
Collier PN, Patel I, Taylor RJ. A concise, stereoselective synthesis of meso-2,6-diaminopimelic acid (DAP) Tetrahedron Letters. 42: 5953-5954. DOI: 10.1016/S0040-4039(01)01150-9 |
0.322 |
|
| 2001 |
McAllister GD, Taylor RJ. The synthesis of polyoxygenated, enantiopure cyclopentene derivatives using the Ramberg–Bäcklund rearrangement Tetrahedron Letters. 42: 1197-1200. DOI: 10.1016/S0040-4039(00)02209-7 |
0.344 |
|
| 2000 |
Papillon JP, Taylor RJ. The first syntheses of the 1-oxo-2-oxa-5-azaspiro[3.4]octane ring system found in oxazolomycin. Organic Letters. 2: 1987-90. PMID 10891211 DOI: 10.1021/Ol0058792 |
0.309 |
|
| 2000 |
Collier PN, Campbell AD, Patel I, Taylor RJ. The direct synthesis of novel enantiomerically pure α-amino acids in protected form via Suzuki cross-coupling Tetrahedron Letters. 41: 7115-7119. DOI: 10.1016/S0040-4039(00)01174-6 |
0.317 |
|
| 1999 |
Murphy PV, Hubbard RE, Manallack DT, Wills RE, Montana JG, Taylor RJ. The design, synthesis, and evaluation of novel conformationally rigid analogues of sialyl Lewis(x). Bioorganic & Medicinal Chemistry. 6: 2421-39. PMID 9925299 DOI: 10.1016/S0968-0896(98)80017-5 |
0.502 |
|
| 1999 |
Campbell AD, Raynham TM, Taylor RJ. The synthesis of novel amino acids via hydroboration-Suzuki cross coupling Tetrahedron Letters. 40: 5263-5266. DOI: 10.1016/S0040-4039(99)00997-1 |
0.31 |
|
| 1999 |
Alcaraz L, Macdonald G, Ragot J, Lewis NJ, Taylor RJ. Synthetic approaches to the Manumycin A, B and C antibiotics: The first total synthesis of (+)-Manumycin A Tetrahedron. 55: 3707-3716. DOI: 10.1016/S0040-4020(98)00879-5 |
0.348 |
|
| 1998 |
Alcaraz M, Griffin FK, Paterson DE, Taylor RJ. Synthetic applications of Ramberg-Bäcklund derived exo-glycals Tetrahedron Letters. 39: 8183-8186. DOI: 10.1016/S0040-4039(98)01823-1 |
0.326 |
|
| 1998 |
Griffin FK, Murphy PV, Paterson DE, Taylor RJ. A Ramberg-Bäcklund approach to exo-glycals Tetrahedron Letters. 39: 8179-8182. DOI: 10.1016/S0040-4039(98)01822-X |
0.526 |
|
| 1998 |
Macdonald G, Alcaraz L, Lewis NJ, Taylor RJ. Asymmetric synthesis of the mC7N core of the manumycin family: Preparation of (+)-MT 35214 and a formal total synthesis of (−)-alisamycin Tetrahedron Letters. 39: 5433-5436. DOI: 10.1016/S0040-4039(98)01047-8 |
0.33 |
|
| 1998 |
Murphy PV, Hubbard RE, Manallack DT, Montana JG, Taylor RJ. The synthesis of novel structural analogues of sialyl Lewisx Tetrahedron Letters. 39: 3273-3276. DOI: 10.1016/S0040-4039(98)00468-7 |
0.55 |
|
| 1998 |
Macdonald G, Alcaraz L, Wei X, Lewis NJ, Taylor RJ. Unsaturated amides derived from 2-amino-3-hydroxycyclopentenone: A stille approach to the synthesis of asuka-mABA, 2880-II, and limocrocin Tetrahedron. 54: 9823-9836. DOI: 10.1016/S0040-4020(98)00536-5 |
0.315 |
|
| 1997 |
Wei X, Taylor RJ. Organolithium additions to styrene derivatives—III.1,2 Enantioselective routes to 2-arylalkanoic acids Tetrahedron: Asymmetry. 8: 665-668. DOI: 10.1016/S0957-4166(97)00032-3 |
0.303 |
|
| 1996 |
Charoenying P, Huw Davies D, McKerrecher D, Taylor RJ. A new stereocontrolled, pyrylium-based route to conjugated dienynes: The first synthesis of carduusyne A Tetrahedron Letters. 37: 1913-1916. DOI: 10.1016/0040-4039(96)00153-0 |
0.345 |
|
| 1996 |
McNaughton-Smith GA, Taylor RJ. The preparation of 9-substituted Δ5-octenolides: Synthesis of 8-deoxy-pseudo-ascidiatrienolide C Tetrahedron. 52: 2113-2124. DOI: 10.1016/0040-4020(95)01028-9 |
0.314 |
|
| 1996 |
Hubbard RE, Montana JG, Murphy PV, Taylor RJ. Glycosylation reactions of 2,3,4-tri-O-chlorosulfonyl-β-l-fucopyranosyl chloride and 2,3,4-tri-O-chlorosulfonyl-β-d-xylopyranosyl chloride Carbohydrate Research. 287: 247-253. DOI: 10.1016/0008-6215(96)00077-8 |
0.461 |
|
| 1994 |
Guo ZX, Haines AH, Pyke SM, Pyke SG, Taylor RJ. Improved preparation of (+/-)-(1,3/2,4)-5-cyclohexene-1,2,3,4-tetrol [(+/-)-conduritol-B] and its reaction with hydrobromic and hydrochloric acid; synthesis and characterisation of some (+/-)-1-deoxy-1-halo- and (+/-)- 1,4-dideoxy-1,4-dihalo-conduritols. Carbohydrate Research. 264: 147-53. PMID 8001016 DOI: 10.1016/0008-6215(94)00188-X |
0.317 |
|
| 1992 |
Davies AJ, Taylor RJ, Scopes DI, Wadsworth AH. The preparation of novel dopamine analogues via palladium catalysed cyclisation reactions Bioorganic & Medicinal Chemistry Letters. 2: 481-484. DOI: 10.1016/S0960-894X(00)80174-2 |
0.31 |
|
| 1989 |
Casy G, Taylor RJ. The synthesis of 2,3-disubstituted cyclopentenones using the ramberg-bäcklund reaction in conjunction with organocopper chemistry Tetrahedron. 45: 455-466. DOI: 10.1016/0040-4020(89)80073-0 |
0.352 |
|
| 1985 |
Furber M, Taylor RJ, Burford S. ,-dienes via acetylene carbocupration: synthesis of navel orangeworm pheromone Tetrahedron Letters. 26: 3285-3288. DOI: 10.1016/S0040-4039(00)98174-7 |
0.302 |
|
| 1985 |
Lane S, Taylor RJ. Conjugate addition to thiin-4-ones; A novel route to thiathromboxane analogues Tetrahedron Letters. 26: 2821-2824. DOI: 10.1016/S0040-4039(00)94922-0 |
0.351 |
|
| 1985 |
Furber M, Taylor RJ, Cliff Burford S. The synthesis of leukotriene analogues via acetylene carbocupration Tetrahedron Letters. 26: 2731-2734. DOI: 10.1016/S0040-4039(00)94897-4 |
0.311 |
|
| 1982 |
Dixon AJ, Taylor RJ, Newton RF, Wadsworth A. 11-deoxyhomoprostacyclin analogues Tetrahedron Letters. 23: 327-330. DOI: 10.1016/S0040-4039(00)86822-7 |
0.347 |
|
| 1975 |
Harrison I, Taylor R, Fried J. Synthesis of 11-thiaprostaglandins Tetrahedron Letters. 16: 1165-1168. DOI: 10.1016/S0040-4039(00)72085-5 |
0.325 |
|
| 1974 |
Jones DN, Lewton DA, Msonthi JD, Taylor RJ. Steroidal sulphur compounds. (part)X1. 4-Thia-5alpha- and 5beta-cholestane and their oxides and dioxides. Journal of the Chemical Society. Perkin Transactions 1. 2637-45. PMID 4477770 |
0.424 |
|
| 1973 |
Jones DN, Blenkinsopp J, Edmonds AC, Helmy E, Taylor RJ. Steroidal sulphur compounds. IX. 6alpha- and 6beta-methylsulphinyl-cholest-4-ene and related compounds; Stereochemical aspects of the allyl sulphoxide-sulphenate rearrangement. Journal of the Chemical Society. Perkin Transactions 1. 21: 2602-13. PMID 4797715 |
0.439 |
|
| 1973 |
Buchanan GL, Raphael RA, Taylor R. A convenient stereoselective synthesis of syn-bishomoquinone (tri-cyclo[5,1,0,0]octane-2,6-dione) Journal of the Chemical Society-Perkin Transactions 1. 373-375. DOI: 10.1039/P19730000373 |
0.346 |
|
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