| Year |
Citation |
Score |
| 2024 |
Stojalnikova V, Webster SJ, Liu K, Fletcher SP. Chelation enables selectivity control in enantioconvergent Suzuki-Miyaura cross-couplings on acyclic allylic systems. Nature Chemistry. PMID 38332329 DOI: 10.1038/s41557-023-01430-8 |
0.342 |
|
| 2023 |
Mishra S, Karabiyikoglu S, Fletcher SP. Catalytic Enantioselective Synthesis of 3-Piperidines from Arylboronic Acids and Pyridine. Journal of the American Chemical Society. 145: 14221-14226. PMID 37345648 DOI: 10.1021/jacs.3c05044 |
0.382 |
|
| 2023 |
Egea-Arrebola D, Goetzke FW, Fletcher SP. Rhodium-Catalyzed Asymmetric Arylation of Cyclobutenone Ketals. Angewandte Chemie (International Ed. in English). PMID 36728888 DOI: 10.1002/anie.202217381 |
0.336 |
|
| 2022 |
Cunningham L, Portela MS, Fletcher SP. Scale-Up of a Rh-Catalyzed Asymmetric sp-sp Suzuki-Miyaura-Type Reaction. Organic Process Research & Development. 26: 3153-3160. PMID 36437898 DOI: 10.1021/acs.oprd.2c00268 |
0.3 |
|
| 2022 |
Zhang Y, Goetzke FW, Christensen KE, Fletcher SP. Asymmetric Synthesis of Nortropanes Rh-Catalyzed Allylic Arylation. Acs Catalysis. 12: 8995-9002. PMID 35966601 DOI: 10.1021/acscatal.2c02259 |
0.321 |
|
| 2021 |
Goetzke FW, Sidera M, Fletcher SP. Catalytic asymmetric hydrometallation of cyclobutenes with salicylaldehydes. Chemical Science. 13: 236-240. PMID 35059172 DOI: 10.1039/d1sc06035j |
0.301 |
|
| 2021 |
Goetzke FW, Hell AML, van Dijk L, Fletcher SP. A catalytic asymmetric cross-coupling approach to the synthesis of cyclobutanes. Nature Chemistry. PMID 34211118 DOI: 10.1038/s41557-021-00725-y |
0.348 |
|
| 2021 |
Babu D, Scanes RJH, Plamont R, Ryabchun A, Lancia F, Kudernac T, Fletcher SP, Katsonis N. Acceleration of lipid reproduction by emergence of microscopic motion. Nature Communications. 12: 2959. PMID 34011926 DOI: 10.1038/s41467-021-23022-1 |
0.566 |
|
| 2020 |
Wang JYJ, Fletcher SP. Synthesis of the Taxol Core via Catalytic Asymmetric 1,4-Addition of an Alkylzirconium Nucleophile. Organic Letters. PMID 32396003 DOI: 10.1021/Acs.Orglett.0C01165 |
0.427 |
|
| 2020 |
Kučera R, Goetzke FW, Fletcher SP. An Asymmetric Suzuki-Miyaura Approach to Prostaglandins: Synthesis of Tafluprost. Organic Letters. PMID 32216289 DOI: 10.1021/Acs.Orglett.0C00745 |
0.421 |
|
| 2020 |
Karabiyikoglu S, Brethomé AV, Palacin T, Paton RS, Fletcher SP. Enantiomerically enriched tetrahydropyridine allyl chlorides Chemical Science. 11: 4125-4130. DOI: 10.1039/D0Sc00377H |
0.393 |
|
| 2019 |
Brethomé AV, Paton RS, Fletcher SP. Retooling Asymmetric Conjugate Additions for Sterically Demanding Substrates with an Iterative Data-Driven Approach. Acs Catalysis. 9: 7179-7187. PMID 32064147 DOI: 10.1021/Acscatal.9B01814 |
0.392 |
|
| 2019 |
González J, Schäfer P, Fletcher SP. Highly Enantioselective Hiyama Cross-Coupling via Rh-Catalyzed Allylic Arylation of Racemic Allyl Chlorides. Organometallics. 38: 3991-3995. PMID 32055086 DOI: 10.1021/Acs.Organomet.9B00197 |
0.427 |
|
| 2019 |
González J, van Dijk L, Goetzke FW, Fletcher SP. Highly enantioselective rhodium-catalyzed cross-coupling of boronic acids and racemic allyl halides. Nature Protocols. 14: 2972-2985. PMID 31541227 DOI: 10.1038/S41596-019-0209-8 |
0.439 |
|
| 2019 |
Goetzke FW, Mortimore M, Fletcher SP. Enantio- and Diastereoselective Suzuki-Miyaura Coupling with Racemic Bicycles. Angewandte Chemie (International Ed. in English). PMID 31246358 DOI: 10.1002/Anie.201906478 |
0.454 |
|
| 2019 |
Jacques R, Pullin RDC, Fletcher SP. Desymmetrization of meso-bisphosphates using copper catalysis and alkylzirconocene nucleophiles. Nature Communications. 10: 21. PMID 30604753 DOI: 10.1038/S41467-018-07871-X |
0.402 |
|
| 2019 |
Jacques R, Hell AM, Pullin RD, Fletcher SP. Desymmetrization of meso-bisphosphates via rhodium catalyzed asymmetric allylic arylation Tetrahedron. 75: 130560. DOI: 10.1016/J.Tet.2019.130560 |
0.454 |
|
| 2018 |
Wang JYJ, Palacin T, Fletcher SP. β-Chloroaldehydes from Trapping Zirconium Enolates Produced in Asymmetric 1,4-Additions. Organic Letters. PMID 30596505 DOI: 10.1021/Acs.Orglett.8B03520 |
0.42 |
|
| 2018 |
Mistry N, Fletcher SP. Catalytic asymmetric synthesis of geminal-dicarboxylates. Chemical Science. 9: 6307-6312. PMID 30123485 DOI: 10.1039/C8Sc01786G |
0.423 |
|
| 2018 |
Post EAJ, Bissette AJ, Fletcher SP. Self-reproducing micelles coupled to a secondary catalyst. Chemical Communications (Cambridge, England). 54: 8777-8780. PMID 30035281 DOI: 10.1039/C8Cc02136H |
0.302 |
|
| 2018 |
Ardkhean R, Mortimore M, Paton RS, Fletcher SP. Formation of quaternary centres by copper catalysed asymmetric conjugate addition to β-substituted cyclopentenones with the aid of a quantitative structure-selectivity relationship. Chemical Science. 9: 2628-2632. PMID 29675255 DOI: 10.1039/C7Sc05304E |
0.335 |
|
| 2018 |
Gao Z, Fletcher SP. Construction of β to carbonyl stereogenic centres by asymmetric 1,4-addition of alkylzirconocenes to dienones and ynenones. Chemical Communications (Cambridge, England). PMID 29568835 DOI: 10.1039/C8Cc01201F |
0.325 |
|
| 2017 |
Schäfer P, Sidera M, Palacin T, Fletcher SP. Asymmetric cross-coupling of alkyl, alkenyl and (hetero)aryl nucleophiles with racemic allyl halides. Chemical Communications (Cambridge, England). PMID 29098227 DOI: 10.1039/C7Cc07151E |
0.371 |
|
| 2017 |
Gao Z, Fletcher SP. Asymmetric conjugate addition of alkylzirconium reagents to α,β-unsaturated thioesters: access to fragrances and acyclic stereochemical arrays. Chemical Communications (Cambridge, England). PMID 28861568 DOI: 10.1039/C7Cc05433E |
0.351 |
|
| 2017 |
Schäfer P, Palacin T, Sidera M, Fletcher SP. Asymmetric Suzuki-Miyaura coupling of heterocycles via Rhodium-catalysed allylic arylation of racemates. Nature Communications. 8: 15762. PMID 28607510 DOI: 10.1038/Ncomms15762 |
0.414 |
|
| 2017 |
Gao Z, Fletcher SP. Acyclic quaternary centers from asymmetric conjugate addition of alkylzirconium reagents to linear trisubstituted enones. Chemical Science. 8: 641-646. PMID 28451211 DOI: 10.1039/C6Sc02811J |
0.374 |
|
| 2017 |
Rideau E, You H, Sidera M, Claridge TD, Fletcher SP. Mechanistic studies on a Cu-catalyzed asymmetric allylic alkylation with cyclic racemic starting materials. Journal of the American Chemical Society. PMID 28362495 DOI: 10.1021/Jacs.7B02440 |
0.381 |
|
| 2017 |
Aßhoff SJ, Lancia F, Iamsaard S, Matt B, Kudernac T, Fletcher SP, Katsonis N. High-Power Actuation from Molecular Photoswitches in Enantiomerically Paired Soft Springs. Angewandte Chemie (International Ed. in English). PMID 28181400 DOI: 10.1002/Anie.201611325 |
0.602 |
|
| 2017 |
Ardkhean R, Roth PMC, Maksymowicz RM, Curran A, Peng Q, Paton RS, Fletcher SP. Enantioselective Conjugate Addition Catalyzed by a Copper Phosphoramidite Complex: Computational and Experimental Exploration of Asymmetric Induction Acs Catalysis. 7: 6729-6737. DOI: 10.1021/Acscatal.7B01453 |
0.334 |
|
| 2016 |
Iamsaard S, Villemin E, Lancia F, Aβhoff SJ, Fletcher SP, Katsonis N. Preparation of biomimetic photoresponsive polymer springs. Nature Protocols. 11: 1788-97. PMID 27583641 DOI: 10.1038/Nprot.2016.087 |
0.605 |
|
| 2016 |
Garrec K, Fletcher SP. Cp2ZrMeCl: A Reagent for Asymmetric Methyl Addition. Organic Letters. PMID 27458650 DOI: 10.1021/Acs.Orglett.6B01829 |
0.403 |
|
| 2016 |
Iamsaard S, Anger E, Aßhoff SJ, Depauw A, Fletcher SP, Katsonis N. Fluorinated Azobenzenes for Shape-Persistent Liquid Crystal Polymer Networks. Angewandte Chemie (International Ed. in English). PMID 27430357 DOI: 10.1002/Anie.201603579 |
0.592 |
|
| 2016 |
Macdonald JP, Sidera M, Fletcher SP, Shaver MP. Living and immortal polymerization of seven and six membered lactones to high molecular weights with aluminum salen and salan catalysts European Polymer Journal. 74: 287-295. DOI: 10.1016/J.Eurpolymj.2015.11.032 |
0.307 |
|
| 2016 |
Mistry N, Fletcher SP. Phosphoramidite Ligands Based on Simple 1,2-Diols: Synthesis, Use in Copper-Catalyzed Asymmetric Additions, and Achirotopic Stereogenic Phosphorus Centres Advanced Synthesis & Catalysis. 358: 2489-2496. DOI: 10.1002/Adsc.201600368 |
0.339 |
|
| 2015 |
Rideau E, Fletcher SP. Copper-catalysed asymmetric allylic alkylation of alkylzirconocenes to racemic 3,6-dihydro-2H-pyrans. Beilstein Journal of Organic Chemistry. 11: 2435-43. PMID 26734091 DOI: 10.3762/Bjoc.11.264 |
0.335 |
|
| 2015 |
Sidera M, Fletcher SP. Rhodium-catalysed asymmetric allylic arylation of racemic halides with arylboronic acids. Nature Chemistry. 7: 935-9. PMID 26492015 DOI: 10.1038/Nchem.2360 |
0.471 |
|
| 2015 |
Sidera M, Fletcher SP. Cu-catalyzed asymmetric addition of sp²-hybridized zirconium nucleophiles to racemic allyl bromides. Chemical Communications (Cambridge, England). 51: 5044-7. PMID 25705853 DOI: 10.1039/C5Cc00421G |
0.386 |
|
| 2015 |
Roth PM, Fletcher SP. Enantioselective copper(I)-phosphoramidite catalyzed addition of alkylzirconium species to acyclic enones. Organic Letters. 17: 912-5. PMID 25634651 DOI: 10.1021/Acs.Orglett.5B00021 |
0.375 |
|
| 2015 |
Maksymowicz RM, Bissette AJ, Fletcher SP. Asymmetric conjugate additions and allylic alkylations using nucleophiles generated by hydro- or carbometallation. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 5668-78. PMID 25603764 DOI: 10.1002/Chem.201405855 |
0.358 |
|
| 2015 |
You H, Rideau E, Sidera M, Fletcher SP. Non-stabilized nucleophiles in Cu-catalysed dynamic kinetic asymmetric allylic alkylation. Nature. 517: 351-5. PMID 25592541 DOI: 10.1038/Nature14089 |
0.42 |
|
| 2015 |
Mola L, Sidera M, Fletcher SP. Asymmetric Remote C-H Functionalization: Use of Internal Olefins in Tandem Hydrometallation-Isomerization-Asymmetric Conjugate Addition Sequences Australian Journal of Chemistry. 68: 401-403. DOI: 10.1071/Ch14556 |
0.357 |
|
| 2015 |
Rideau E, Mäsing F, Fletcher SP. Asymmetric Conjugate Addition of Alkylzirconocenes to Cyclopent-4-ene-1,3-dione Monoacetals Synthesis (Germany). 47: 2217-2222. DOI: 10.1055/S-0034-1379928 |
0.423 |
|
| 2015 |
Anger E, Fletcher SP. Simple azo dyes provide access to versatile chiroptical switches European Journal of Organic Chemistry. 2015: 3651-3655. DOI: 10.1002/Ejoc.201500485 |
0.332 |
|
| 2015 |
Maksymowicz RM, Bissette AJ, Fletcher SP. Asymmetric conjugate additions and allylic alkylations using nucleophiles generated by hydro- or carbometallation Chemistry - a European Journal. 21: 5668-5678. DOI: 10.1002/chem.201405855 |
0.317 |
|
| 2014 |
Bissette AJ, Odell B, Fletcher SP. Physical autocatalysis driven by a bond-forming thiol-ene reaction. Nature Communications. 5: 4607. PMID 25178358 DOI: 10.1038/Ncomms5607 |
0.311 |
|
| 2014 |
Maciver EE, Maksymowicz RM, Wilkinson N, Roth PM, Fletcher SP. Asymmetric conjugate addition of alkylzirconium reagents to α,β-unsaturated lactones. Organic Letters. 16: 3288-91. PMID 24893570 DOI: 10.1021/Ol501292X |
0.345 |
|
| 2014 |
Iamsaard S, Aßhoff SJ, Matt B, Kudernac T, Cornelissen JJ, Fletcher SP, Katsonis N. Conversion of light into macroscopic helical motion. Nature Chemistry. 6: 229-35. PMID 24557138 DOI: 10.1038/Nchem.1859 |
0.6 |
|
| 2014 |
Bassolino G, Sovdat T, Liebel M, Schnedermann C, Odell B, Claridge TDW, Kukura P, Fletcher SP. Synthetic control of retinal photochemistry and photophysics in solution Journal of the American Chemical Society. 136: 2650-2658. PMID 24479840 DOI: 10.1021/Ja4121814 |
0.314 |
|
| 2014 |
Roth PMC, Sidera M, Maksymowicz RM, Fletcher SP. Copper-catalyzed asymmetric conjugate addition of alkylzirconium reagents to cyclic enones to form quaternary centers Nature Protocols. 9: 104-111. PMID 24336474 DOI: 10.1038/Nprot.2013.169 |
0.38 |
|
| 2013 |
Sidera M, Roth PM, Maksymowicz RM, Fletcher SP. Formation of quaternary centers by copper-catalyzed asymmetric conjugate addition of alkylzirconium reagents. Angewandte Chemie (International Ed. in English). 52: 7995-9. PMID 23780788 DOI: 10.1002/Anie.201303202 |
0.385 |
|
| 2013 |
Maksymowicz RM, Roth PM, Thompson AL, Fletcher SP. Hydrometallation-asymmetric conjugate addition: application to complex molecule synthesis. Chemical Communications (Cambridge, England). 49: 4211-3. PMID 23192003 DOI: 10.1039/C2Cc37155C |
0.41 |
|
| 2013 |
Maksymowicz RM, Sidera M, Roth PMC, Fletcher SP. A convenient catalytic asymmetric conjugate addition reaction to enones using alkylzirconium reagents Synthesis (Germany). 45: 2662-2668. DOI: 10.1055/S-0033-1339485 |
0.355 |
|
| 2012 |
Maksymowicz RM, Roth PM, Fletcher SP. Catalytic asymmetric carbon-carbon bond formation using alkenes as alkylmetal equivalents. Nature Chemistry. 4: 649-54. PMID 22824897 DOI: 10.1038/Nchem.1394 |
0.353 |
|
| 2011 |
Fletcher SP, Solà J, Holt D, Brown RA, Clayden J. Synthesis of enantiomerically enriched (R)-C-labelled 2-aminoisobutyric acid (Aib) by conformational memory in the alkylation of a derivative of L-alanine. Beilstein Journal of Organic Chemistry. 7: 1304-9. PMID 22043239 DOI: 10.3762/Bjoc.7.152 |
0.668 |
|
| 2011 |
Mao B, Geurts K, Fañanás-Mastral M, van Zijl AW, Fletcher SP, Minnaard AJ, Feringa BL. Catalytic enantioselective synthesis of naturally occurring butenolides via hetero-allylic alkylation and ring closing metathesis. Organic Letters. 13: 948-51. PMID 21268603 DOI: 10.1021/Ol102994Q |
0.559 |
|
| 2011 |
Mao B, Geurts K, Fañanás-Mastral M, Zijl AWv, Fletcher SP, Minnaard AJ, Feringa BL. Asymmetric Synthesis of γ-Butenolides via SequentialMetal-Catalyzed Reactions Synfacts. 2011: 639-639. DOI: 10.1055/S-0030-1260438 |
0.378 |
|
| 2010 |
Solà J, Fletcher SP, Castellanos A, Clayden J. Nanometer-range communication of stereochemical information by reversible switching of molecular helicity. Angewandte Chemie (International Ed. in English). 49: 6836-9. PMID 20687056 DOI: 10.1002/Anie.201001130 |
0.593 |
|
| 2010 |
Clayden J, Fletcher SP, Senior J, Worrall CP. Hindered diarylether and diarylsulfone bisphosphine ligands: Atropisomerism and palladium complexes Tetrahedron Asymmetry. 21: 1355-1360. DOI: 10.1016/J.Tetasy.2010.06.017 |
0.487 |
|
| 2009 |
Fletcher SP. Building blocks of life: Growing the seeds of homochirality Nature Chemistry. 1: 692-693. PMID 21124355 DOI: 10.1038/Nchem.455 |
0.328 |
|
| 2009 |
Clayden J, Fletcher SP, Rowbottom SJ, Helliwell M. Conformational preferences of a polar biaryl: a phase- and enantiomeric purity-dependent molecular hinge. Organic Letters. 11: 2313-6. PMID 19435372 DOI: 10.1021/Ol9006635 |
0.451 |
|
| 2009 |
Clayden J, Fletcher SP, McDouall JJ, Rowbottom SJ. Controlling axial conformation in 2-arylpyridines and 1-arylisoquinolines: application to the asymmetric synthesis of QUINAP by dynamic thermodynamic resolution. Journal of the American Chemical Society. 131: 5331-43. PMID 19309078 DOI: 10.1021/Ja900722Q |
0.502 |
|
| 2008 |
Clive DL, Peng J, Fletcher SP, Ziffle VE, Wingert D. Synthesis of diverse 2,3-dihydroindoles, 1,2,3,4-tetrahydroquinolines, and benzo-fused azepines by formal radical cyclization onto aromatic rings. The Journal of Organic Chemistry. 73: 2330-44. PMID 18278944 DOI: 10.1021/Jo7026307 |
0.725 |
|
| 2008 |
Geurts K, Fletcher SP, Van Zijl AW, Minnaard AJ, Feringa BL. Copper-catalyzed asymmetric allylic substitution reactions with organozinc and Grignard reagents Pure and Applied Chemistry. 80: 1025-1037. DOI: 10.1351/Pac200880051025 |
0.535 |
|
| 2007 |
Fletcher SP, Jagt RB, Feringa BL. An astrophysically-relevant mechanism for amino acid enantiomer enrichment. Chemical Communications (Cambridge, England). 2578-80. PMID 17579743 DOI: 10.1039/B702882B |
0.745 |
|
| 2007 |
Feringa B, Howell G, Fletcher S, Geurts K, ter Horst B. Synthesis of (-)-Phaseolinic Acid Synfacts. 2007: 0349-0349. DOI: 10.1055/S-2007-968290 |
0.515 |
|
| 2007 |
Feringa B, Geurts K, Fletcher S. Cu-Catalyzed Asymmetric Synthesis of Chiral Allylic Esters Synfacts. 2007: 0310-0310. DOI: 10.1055/S-2007-968177 |
0.482 |
|
| 2006 |
Geurts K, Fletcher SP, Feringa BL. Copper catalyzed asymmetric synthesis of chiral allylic esters. Journal of the American Chemical Society. 128: 15572-3. PMID 17147350 DOI: 10.1021/Ja065780B |
0.548 |
|
| 2006 |
Howell GP, Fletcher SP, Geurts K, ter Horst B, Feringa BL. Catalytic asymmetric synthesis of acyclic arrays by tandem 1,4-addition-aldol reactions. Journal of the American Chemical Society. 128: 14977-85. PMID 17105309 DOI: 10.1021/Ja0651862 |
0.535 |
|
| 2005 |
Fletcher SP, Dumur F, Pollard MM, Feringa BL. A reversible, unidirectional molecular rotary motor driven by chemical energy. Science (New York, N.Y.). 310: 80-2. PMID 16210531 DOI: 10.1126/Science.1117090 |
0.395 |
|
| 2005 |
Fletcher SP, Clive DL, Peng J, Wingert DA. Oxidation of p-aminophenols and formal radical cyclization onto benzene rings: formation of benzo-fused nitrogen heterocycles. Organic Letters. 7: 23-6. PMID 15624968 DOI: 10.1021/Ol047977J |
0.717 |
|
| 2004 |
Clive DL, Fletcher SP, Liu D. Formal radical cyclization onto benzene rings: a general method and its use in the synthesis of ent-nocardione A. The Journal of Organic Chemistry. 69: 3282-93. PMID 15132533 DOI: 10.1021/Jo030364K |
0.694 |
|
| 2003 |
Clive DL, Fletcher SP. Synthesis of (+)-nocardione A--use of formal radical cyclization onto a benzene ring. Chemical Communications (Cambridge, England). 2464-5. PMID 14587733 DOI: 10.1039/B307937F |
0.692 |
|
| 2003 |
Clive DL, Fletcher SP, Zhu M. Formal radical cyclization onto benzene rings--a general method proceeding via cross-conjugated dienones. Chemical Communications (Cambridge, England). 526-7. PMID 12638982 DOI: 10.1039/B212223E |
0.685 |
|
| 2003 |
Clive DLJ, Fletcher SP. Synthesis of (+)-nocardione A - Use of formal radical cyclization onto a benzene ring Chemical Communications. 9: 2464-2465. |
0.313 |
|
| 2002 |
Clive DL, Fletcher SP. Synthesis of the bicyclic dienone core of the antitumor agent ottelione B. Chemical Communications (Cambridge, England). 1940-1. PMID 12271684 DOI: 10.1039/B205753K |
0.615 |
|
| 1984 |
Taylor E, Palmer D, George T, Fletcher S, Tseng C, Harrington P, Beardsley G. Additions and Corrections - Synthesis and Biological Activity of L-5 Deazafolic Acid and 1,5-Deazaaminopterin: Synthetic Strategies to 5-Deazapteridines. The Journal of Organic Chemistry. 49: 1472-1472. DOI: 10.1021/Jo00182A604 |
0.339 |
|
| 1978 |
Barradas RG, Fletcher S, Porter JD. The electrochemical formation of mercuric oxide in alkaline solution Canadian Journal of Chemistry. 56: 336-342. DOI: 10.1139/V78-052 |
0.301 |
|
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