Year |
Citation |
Score |
2023 |
Agasti S, Beltran F, Pye E, Kaltsoyannis N, Crisenza GEM, Procter DJ. A catalytic alkene insertion approach to bicyclo[2.1.1]hexane bioisosteres. Nature Chemistry. PMID 36781910 DOI: 10.1038/s41557-023-01135-y |
0.738 |
|
2022 |
Dewanji A, van Dalsen L, Rossi-Ashton JA, Gasson E, Crisenza GEM, Procter DJ. A general arene C-H functionalization strategy via electron donor-acceptor complex photoactivation. Nature Chemistry. PMID 36471045 DOI: 10.1038/s41557-022-01092-y |
0.739 |
|
2022 |
Morrill C, Péter Á, Amalina I, Pye E, Crisenza GEM, Kaltsoyannis N, Procter DJ. Diastereoselective Radical 1,4-Ester Migration: Radical Cyclizations of Acyclic Esters with SmI. Journal of the American Chemical Society. 144: 13946-13952. PMID 35858251 DOI: 10.1021/jacs.2c05972 |
0.826 |
|
2022 |
Péter Á, Crisenza GEM, Procter DJ. Asymmetric Total Synthesis of (-)-Phaeocaulisin A. Journal of the American Chemical Society. PMID 35417150 DOI: 10.1021/jacs.2c02188 |
0.804 |
|
2021 |
Péter Á, Agasti S, Knowles O, Pye E, Procter DJ. Recent advances in the chemistry of ketyl radicals. Chemical Society Reviews. 50: 5349-5365. PMID 33972956 DOI: 10.1039/d0cs00358a |
0.815 |
|
2021 |
Dherbassy Q, Manna S, Shi C, Prasitwatcharakorn W, Crisenza G, Perry G, Procter DJ. Enantioselective copper-catalyzed borylative cyclization for the synthesis of quinazolinones. Angewandte Chemie (International Ed. in English). PMID 33847459 DOI: 10.1002/anie.202103259 |
0.784 |
|
2021 |
Agasti S, Beattie NA, McDouall JJW, Procter DJ. SmI-Catalyzed Intermolecular Coupling of Cyclopropyl Ketones and Alkynes: A Link between Ketone Conformation and Reactivity. Journal of the American Chemical Society. 143: 3655-3661. PMID 33629852 DOI: 10.1021/jacs.1c01356 |
0.744 |
|
2020 |
Dherbassy Q, Manna S, Talbot FJT, Prasitwatcharakorn W, Perry GJP, Procter DJ. Copper-catalyzed functionalization of enynes. Chemical Science. 11: 11380-11393. PMID 34094380 DOI: 10.1039/d0sc04012f |
0.717 |
|
2020 |
Kiraly P, Kern N, Plesniak MP, Nilsson M, Procter DJ, Morris GA, Adams RW. Needles from haystacks: single-scan selective excitation of individual NMR signals in overlapping multiplets. Angewandte Chemie (International Ed. in English). PMID 32965750 DOI: 10.1002/anie.202011642 |
0.748 |
|
2020 |
Talbot F, Dherbassy Q, Manna S, Shi C, Zhang S, Howell GP, Perry G, Procter DJ. Copper-Catalyzed Borylative Couplings with C-N Electrophiles. Angewandte Chemie (International Ed. in English). PMID 32544295 DOI: 10.1002/Anie.202007251 |
0.73 |
|
2020 |
Wang D, Carlton CG, Tayu M, McDouall JJW, Perry GJP, Procter DJ. Trifluoromethyl sulfoxides: New reagents for metal-free C-H trifluoromethylthiolation. Angewandte Chemie (International Ed. in English). PMID 32463942 DOI: 10.1002/Anie.202005531 |
0.353 |
|
2020 |
Péter Á, Procter DJ. Cascades, Catalysis and Chiral Ligand Control with SmI₂; The Rebirth of a Reagent. Chimia. 74: 18-22. PMID 32200782 DOI: 10.2533/Chimia.2020.18 |
0.82 |
|
2020 |
Manna S, Dherbassy Q, Perry GJP, Procter DJ. Enantio- and Diastereoselective Synthesis of Homopropargyl Amines by Copper-Catalyzed Coupling of Imines, 1,3-Enynes, and Diborons. Angewandte Chemie (International Ed. in English). PMID 31917893 DOI: 10.1002/Anie.201915191 |
0.737 |
|
2020 |
He Z, Perry GJP, Procter DJ. Sulfoxide-mediated oxidative cross-coupling of phenols Chemical Science. 11: 2001-2005. DOI: 10.1039/C9Sc05668H |
0.336 |
|
2020 |
He Z, Biremond T, Perry GJP, Procter DJ. Para-coupling of phenols with C2/C3-substituted benzothiophene S-oxides Tetrahedron. 131315. DOI: 10.1016/J.Tet.2020.131315 |
0.35 |
|
2020 |
Péter Á, Perry GJP, Procter DJ. Radical C–C bond formation using sulfonium salts and light Advanced Synthesis & Catalysis. 362: 2135-2142. DOI: 10.1002/Adsc.202000220 |
0.323 |
|
2019 |
Yan J, Pulis AP, Perry GJP, Procter DJ. Metal-free synthesis of benzothiophenes via 2-fold C-H functionalization: direct access to materials-oriented heteroaromatics. Angewandte Chemie (International Ed. in English). PMID 31479175 DOI: 10.1002/Anie.201908319 |
0.395 |
|
2019 |
Huang HM, Garduño-Castro MH, Morrill C, Procter DJ. Catalytic cascade reactions by radical relay. Chemical Society Reviews. PMID 31298671 DOI: 10.1039/C8Cs00947C |
0.782 |
|
2019 |
Marshall SA, Payne KAP, Fisher K, Gahloth D, Bailey SS, Balaikaite A, Saaret A, Gostimskaya I, Aleku G, Huang H, Rigby SEJ, Procter D, Leys D. Heterologous production, reconstitution and EPR spectroscopic analysis of prFMN dependent enzymes. Methods in Enzymology. 620: 489-508. PMID 31072499 DOI: 10.1016/Bs.Mie.2019.03.022 |
0.726 |
|
2019 |
Šiaučiulis M, Ahlsten N, Pulis AP, Procter DJ. Transition-Metal-Free Cross-Coupling of Benzothiophenes and Styrenes in a Stereoselective Synthesis of Substituted (E,Z)-1,3-Dienes. Angewandte Chemie (International Ed. in English). PMID 30964596 DOI: 10.1002/Anie.201902903 |
0.408 |
|
2019 |
He Z, Pulis AP, Procter DJ. The interrupted Pummerer reaction in a sulfoxide-catalyzed oxidative coupling of 2-naphthols. Angewandte Chemie (International Ed. in English). PMID 30958633 DOI: 10.1002/Anie.201903492 |
0.42 |
|
2019 |
He Z, Pulis AP, Perry GJP, Procter DJ. Pummerer chemistry of benzothiophene S-oxides: Metal-free alkylation and arylation of benzothiophenes Phosphorus, Sulfur, and Silicon and the Related Elements. 194: 669-677. DOI: 10.1080/10426507.2019.1602626 |
0.335 |
|
2019 |
Huang H, He Q, Procter DJ. Samarium Diiodide Catalyzed Radical Cascade Cyclizations that Construct Quaternary Stereocenters Synlett. 31: 45-50. DOI: 10.1055/S-0039-1690196 |
0.794 |
|
2019 |
Huang H, McDouall JJW, Procter DJ. SmI2-catalysed cyclization cascades by radical relay Nature Catalysis. 2: 211-218. DOI: 10.1038/s41929-018-0219-x |
0.757 |
|
2019 |
Perry GJP, Jia T, Procter DJ. Copper-Catalyzed Functionalization of 1,3-Dienes: Hydrofunctionalization, Borofunctionalization, and Difunctionalization Acs Catalysis. 10: 1485-1499. DOI: 10.1021/Acscatal.9B04767 |
0.363 |
|
2019 |
Jia T, Smith MJ, Pulis AP, Perry GJP, Procter DJ. Enantioselective and Regioselective Copper-Catalyzed Borocyanation of 1-Aryl-1,3-Butadienes Acs Catalysis. 9: 6744-6750. DOI: 10.1021/Acscatal.9B01911 |
0.41 |
|
2019 |
Yeung K, Talbot FJT, Howell GP, Pulis AP, Procter DJ. Copper-Catalyzed Borylative Multicomponent Synthesis of Quaternary α-Amino Esters Acs Catalysis. 9: 1655-1661. DOI: 10.1021/Acscatal.8B04563 |
0.377 |
|
2018 |
Plesniak MP, Garduño-Castro MH, Lenz P, Just-Baringo X, Procter DJ. Samarium(II) folding cascades involving hydrogen atom transfer for the synthesis of complex polycycles. Nature Communications. 9: 4802. PMID 30442955 DOI: 10.1038/S41467-018-07194-X |
0.441 |
|
2018 |
Yang K, Pulis AP, Perry GJP, Procter DJ. Transition-Metal-Free Synthesis of C3-Arylated Benzofurans from Benzothiophenes and Phenols. Organic Letters. PMID 30427186 DOI: 10.1021/Acs.Orglett.8B03267 |
0.436 |
|
2018 |
Huang HM, Adams RW, Procter DJ. Reductive cyclisations of amidines involving aminal radicals. Chemical Communications (Cambridge, England). PMID 30132765 DOI: 10.1039/C8Cc05178J |
0.822 |
|
2018 |
Jia T, He Q, Ruscoe RE, Pulis AP, Procter DJ. Regiodivergent copper catalyzed borocyanation of 1,3-dienes. Angewandte Chemie (International Ed. in English). PMID 29992705 DOI: 10.1002/Anie.201806169 |
0.379 |
|
2018 |
Aukland MH, Talbot FJT, Fernández-Salas JA, Ball M, Pulis AP, Procter DJ. An Interrupted Pummerer/Nickel-Catalysed Cross-Coupling Sequence. Angewandte Chemie (International Ed. in English). PMID 29882623 DOI: 10.1002/Anie.201805396 |
0.361 |
|
2018 |
Šiaučiulis M, Sapmaz S, Pulis AP, Procter DJ. Dual vicinal functionalisation of heterocycles an interrupted Pummerer coupling/[3,3]-sigmatropic rearrangement cascade. Chemical Science. 9: 754-759. PMID 29629145 DOI: 10.1039/C7Sc04723A |
0.44 |
|
2018 |
He Z, Shrives H, Fernández-Salas JA, Abengózar A, Neufeld J, Yang K, Pulis AP, Procter DJ. Synthesis of C2 Substituted Benzothiophenes via an Interrupted Pummerer/[3,3]-Sigmatropic/1,2-Migration Cascade of Benzothiophene S-Oxides. Angewandte Chemie (International Ed. in English). PMID 29528177 DOI: 10.1002/Anie.201801982 |
0.456 |
|
2018 |
Huang HM, McDouall J, Procter DJ. Radical Anions from Urea-type Carbonyls: Radical Cyclizations and Cyclization Cascades. Angewandte Chemie (International Ed. in English). PMID 29493858 DOI: 10.1002/Anie.201800667 |
0.789 |
|
2018 |
Morrill C, Jensen C, Just-Baringo X, Grogan G, Turner N, Procter DJ. Biocatalytic conversion of cyclic ketones bearing alpha-quaternary stereocenters to lactones in an enantioselective radical approach to medium-sized carbocycles. Angewandte Chemie (International Ed. in English). PMID 29393988 DOI: 10.1002/Anie.201800121 |
0.396 |
|
2018 |
Huang H, Procter DJ. Selective Electron Transfer Reduction of Urea-Type Carbonyls European Journal of Organic Chemistry. 2019: 313-317. DOI: 10.1002/Ejoc.201800794 |
0.735 |
|
2017 |
Kern N, Plesniak MP, McDouall JJW, Procter DJ. Enantioselective cyclizations and cyclization cascades of samarium ketyl radicals. Nature Chemistry. 9: 1198-1204. PMID 29168498 DOI: 10.1038/Nchem.2841 |
0.826 |
|
2017 |
Pulis AP, Yeung K, Procter DJ. Enantioselective copper catalysed, direct functionalisation of allenes via allyl copper intermediates. Chemical Science. 8: 5240-5247. PMID 28959423 DOI: 10.1039/C7Sc01968H |
0.41 |
|
2017 |
Huang HM, Procter DJ. Radical heterocyclization and heterocyclization cascades triggered by electron transfer to amide-type carbonyls. Angewandte Chemie (International Ed. in English). PMID 28940768 DOI: 10.1002/Anie.201708354 |
0.785 |
|
2017 |
Huang HM, Bonilla P, Procter DJ. Selective construction of quaternary stereocentres in radical cyclisation cascades triggered by electron-transfer reduction of amide-type carbonyls. Organic & Biomolecular Chemistry. PMID 28426047 DOI: 10.1039/C7Ob00739F |
0.779 |
|
2017 |
Shrives HJ, Fernández-Salas JA, Hedtke C, Pulis AP, Procter DJ. Regioselective synthesis of C3 alkylated and arylated benzothiophenes. Nature Communications. 8: 14801. PMID 28317882 DOI: 10.1038/Ncomms14801 |
0.354 |
|
2017 |
Plesniak MP, Huang H, Procter DJ. Radical cascade reactions triggered by single electron transfer Nature Reviews Chemistry. 1. DOI: 10.1038/s41570-017-0077 |
0.756 |
|
2016 |
Eberhart AJ, Shrives H, Zhang Y, Carrër A, Parry AVS, Tate DJ, Turner ML, Procter DJ. Sulfoxide-directed metal-free cross-couplings in the expedient synthesis of benzothiophene-based components of materials. Chemical Science. 7: 1281-1285. PMID 29910885 DOI: 10.1039/C5Sc03823E |
0.311 |
|
2016 |
Huang HM, Procter DJ. Dearomatizing radical cyclizations and cyclization cascades triggered by electron-transfer reduction of amide-type carbonyls. Journal of the American Chemical Society. PMID 27995785 DOI: 10.1021/Jacs.6B12077 |
0.797 |
|
2016 |
Thurow S, Lenardão EJ, Just-Baringo X, Procter DJ. Reduction of Selenoamides to Amines Using SmI2-H2O. Organic Letters. PMID 27935310 DOI: 10.1021/Acs.Orglett.6B03325 |
0.415 |
|
2016 |
Plesniak MP, Just-Baringo X, Ortu F, Mills DP, Procter DJ. SmCp(R)2-mediated cross-coupling of allyl and propargyl ethers with ketoesters and a telescoped approach to complex cycloheptanols. Chemical Communications (Cambridge, England). PMID 27803945 DOI: 10.1039/C6Cc07318B |
0.347 |
|
2016 |
Fernández-Salas JA, Pulis AP, Procter DJ. Metal-free C-H thioarylation of arenes using sulfoxides: a direct, general diaryl sulfide synthesis. Chemical Communications (Cambridge, England). 52: 12364-12367. PMID 27722278 DOI: 10.1039/C6Cc07627K |
0.373 |
|
2016 |
Just-Baringo X, Clark J, Gutmann MJ, Procter DJ. Selective Synthesis of Cyclooctanoids by Radical Cyclization of Seven-Membered Lactones: Neutron Diffraction Study of the Stereoselective Deuteration of a Chiral Organosamarium Intermediate. Angewandte Chemie (International Ed. in English). PMID 27600354 DOI: 10.1002/Anie.201606792 |
0.481 |
|
2016 |
Yeung K, Ruscoe RE, Rae J, Pulis AP, Procter DJ. Enantioselective Generation of Adjacent Stereocenters in a Copper-Catalyzed Three-Component Coupling of Imines, Allenes, and Diboranes. Angewandte Chemie (International Ed. in English). PMID 27539673 DOI: 10.1002/Anie.201606710 |
0.392 |
|
2016 |
Pulis AP, Procter DJ. C-H Coupling Reactions Directed by Sulfoxides: Teaching an Old Functional Group New Tricks. Angewandte Chemie (International Ed. in English). PMID 27409984 DOI: 10.1002/Anie.201601540 |
0.32 |
|
2016 |
Huang H, Procter DJ. Radical-radical cyclization cascades of barbiturates triggered by electron-transfer reduction of amide-type carbonyls. Journal of the American Chemical Society. PMID 27243379 DOI: 10.1021/Jacs.6B04086 |
0.793 |
|
2016 |
Cavanagh CW, Aukland MH, Laurent Q, Hennessy A, Procter DJ. Iron-mediated oxidative C-H coupling of arenes and alkenes directed by sulfur: an expedient route to dihydrobenzofurans. Organic & Biomolecular Chemistry. PMID 27198174 DOI: 10.1039/C6Ob00883F |
0.359 |
|
2016 |
Zhao X, Perrin L, Procter DJ, Maron L. The role of H2O in the electron transfer-activation of substrates using SmI2: insights from DFT. Dalton Transactions (Cambridge, England : 2003). PMID 26865402 DOI: 10.1039/C6Dt00241B |
0.37 |
|
2016 |
Fernández-Salas JA, Eberhart AJ, Procter DJ. Metal-free CH-CH-type cross coupling of arenes and alkynes di-rected by a multi-functional sulfoxide group. Journal of the American Chemical Society. PMID 26745643 DOI: 10.1021/Jacs.5B12579 |
0.331 |
|
2016 |
Just-Baringo X, Morrill C, Procter DJ. Highly selective SmI2-H2O-promoted radical cyclisation of five-membered lactones Tetrahedron. DOI: 10.1016/J.Tet.2016.03.056 |
0.473 |
|
2015 |
Rae J, Yeung K, McDouall JJ, Procter DJ. Copper-Catalyzed Borylative Cross-Coupling of Allenes and Imines: Selective Three-Component Assembly of Branched Homoallyl Amines. Angewandte Chemie (International Ed. in English). PMID 26632675 DOI: 10.1002/Anie.201508959 |
0.387 |
|
2015 |
Ruscoe RE, Fazakerley NJ, Huang H, Flitsch S, Procter DJ. Copper-catalyzed double additions and radical cyclization cascades in the re-engineering of the antibacterial pleuromutilin. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26527052 DOI: 10.1002/Chem.201504343 |
0.777 |
|
2015 |
Cavanagh CW, Aukland MH, Hennessy A, Procter DJ. Iron-mediated C-H coupling of arenes and unactivated terminal alkenes directed by sulfur. Chemical Communications (Cambridge, England). 51: 9272-5. PMID 25959365 DOI: 10.1039/C5Cc02676H |
0.403 |
|
2015 |
Just-Baringo X, Procter DJ. Sm(II)-Mediated Electron Transfer to Carboxylic Acid Derivatives: Development of Complexity-Generating Cascades. Accounts of Chemical Research. 48: 1263-75. PMID 25871998 DOI: 10.1021/Acs.Accounts.5B00083 |
0.466 |
|
2015 |
Eberhart AJ, Shrives HJ, Álvarez E, Carrër A, Zhang Y, Procter DJ. Sulfoxide-Directed Metal-Free ortho-Propargylation of Aromatics and Heteroaromatics. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 7428-34. PMID 25752800 DOI: 10.1002/Chem.201406424 |
0.408 |
|
2014 |
Szostak M, Spain M, Sautier B, Procter DJ. Switching between reaction pathways by an alcohol cosolvent effect: SmI2-ethylene glycol VS SmI2-H2O mediated synthesis of uracils Organic Letters. 16: 5694-5697. PMID 25343692 DOI: 10.1021/Ol502775W |
0.422 |
|
2014 |
Szostak M, Spain M, Procter DJ. Selective synthesis of α,α-dideuterio alcohols by the reduction of carboxylic acids using Smi2 and D2O as deuterium source under set conditions Organic Letters. 16: 5052-5055. PMID 25247236 DOI: 10.1021/Ol502404E |
0.374 |
|
2014 |
Szostak M, Spain M, Eberhart AJ, Procter DJ. Mechanism of SmI2/amine/H2O-promoted chemoselective reductions of carboxylic acid derivatives (esters, acids, and amides) to alcohols. The Journal of Organic Chemistry. 79: 11988-2003. PMID 25232891 DOI: 10.1021/Jo5018525 |
0.409 |
|
2014 |
Yalavac I, Lyons SE, Webb MR, Procter DJ. SmI2-H2O-mediated 5-exo/6-exo lactone radical cyclisation cascades Chemical Communications. 50: 12863-12866. PMID 25211167 DOI: 10.1039/C4Cc05404K |
0.462 |
|
2014 |
Rae J, Hu YC, Procter DJ. Cu(I)-NHC-catalyzed silylation of allenes: diastereoselective three-component coupling with aldehydes. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 13143-5. PMID 25146221 DOI: 10.1002/Chem.201404330 |
0.394 |
|
2014 |
Szostak M, Lyons SE, Spain M, Procter DJ. Mechanistic investigation of the selective reduction of Meldrum's acids to β-hydroxy acids using SmI2 and H2O Chemical Communications. 50: 8391-8394. PMID 24942543 DOI: 10.1039/C4Cc03216K |
0.416 |
|
2014 |
An J, Work DN, Kenyon C, Procter DJ. Evaluating a sodium dispersion reagent for the Bouveault-Blanc reduction of esters. The Journal of Organic Chemistry. 79: 6743-7. PMID 24941291 DOI: 10.1021/Jo501093G |
0.552 |
|
2014 |
Szostak M, Spain M, Procter DJ. Ketyl-type radicals from cyclic and acyclic esters are stabilized by SmI2(H2O)n: the role of SmI2(H2O)n in post-electron transfer steps. Journal of the American Chemical Society. 136: 8459-66. PMID 24810096 DOI: 10.1021/Ja503494B |
0.476 |
|
2014 |
Szostak M, Fazakerley NJ, Parmar D, Procter DJ. Cross-coupling reactions using samarium(II) iodide. Chemical Reviews. 114: 5959-6039. PMID 24758360 DOI: 10.1021/Cr400685R |
0.335 |
|
2014 |
Levick MT, Grace I, Dai SY, Kasch N, Muryn C, Lambert C, Turner ML, Procter DJ. A Sm(II)-mediated cascade approach to dibenzoindolo[3,2-b]carbazoles: synthesis and evaluation. Organic Letters. 16: 2292-5. PMID 24712719 DOI: 10.1021/Ol500841B |
0.35 |
|
2014 |
Szostak M, Spain M, Procter DJ. On the role of pre- and post-electron-transfer steps in the SmI2 /amine/H(2)O-mediated reduction of esters: new mechanistic insights and kinetic studies. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 4222-6. PMID 24615806 DOI: 10.1002/Chem.201400295 |
0.489 |
|
2014 |
Szostak M, Spain M, Procter DJ. Determination of the effective redox potentials of SmI2, SmBr2, SmCl2, and their complexes with water by reduction of aromatic hydrocarbons. Reduction of anthracene and stilbene by samarium(II) iodide-water complex Journal of Organic Chemistry. 79: 2522-2537. PMID 24517639 DOI: 10.1021/Jo4028243 |
0.367 |
|
2014 |
Szostak M, Sautier B, Spain M, Procter DJ. Electron transfer reduction of nitriles using SmI2-Et 3N-H2O: Synthetic utility and mechanism Organic Letters. 16: 1092-1095. PMID 24494855 DOI: 10.1021/Ol403668E |
0.446 |
|
2014 |
Szostak M, Sautier B, Procter DJ. Structural analysis and reactivity of unusual tetrahedral intermediates enabled by SmI2-mediated reduction of barbituric acids: vinylogous N-acyliminium additions to α-hydroxy-N-acyl-carbamides. Chemical Communications (Cambridge, England). 50: 2518-21. PMID 24463565 DOI: 10.1039/C3Cc48932A |
0.372 |
|
2014 |
Szostak M, Spain M, Eberhart AJ, Procter DJ. Highly chemoselective reduction of amides (primary, secondary, tertiary) to alcohols using SmI2/amine/H2O under mild conditions Journal of the American Chemical Society. 136: 2268-2271. PMID 24460078 DOI: 10.1021/Ja412578T |
0.411 |
|
2014 |
Szostak M, Sautier B, Procter DJ. Stereoselective capture of n-acyliminium ions generated from a-hydroxy-n-acylcarbamides: Direct synthesis of uracils from barbituric acids enabled by smi2 reduction Organic Letters. 16: 452-455. PMID 24359321 DOI: 10.1021/Ol403340J |
0.425 |
|
2014 |
Pace V, Rae JP, Procter DJ. Cu(I)-NHC catalyzed asymmetric silyl transfer to unsaturated lactams and amides. Organic Letters. 16: 476-9. PMID 24350760 DOI: 10.1021/Ol4033623 |
0.328 |
|
2014 |
Fazakerley NJ, Procter DJ. Synthesis and synthetic chemistry of pleuromutilin Tetrahedron. 70: 6911-6930. DOI: 10.1016/J.Tet.2014.05.092 |
0.302 |
|
2013 |
Szostak M, Sautier B, Spain M, Behlendorf M, Procter DJ. Selective reduction of barbituric acids using SmI2/H 2O: Synthesis, reactivity, and structural analysis of tetrahedral adducts Angewandte Chemie - International Edition. 52: 12559-12563. PMID 24123558 DOI: 10.1002/Anie.201306484 |
0.395 |
|
2013 |
Szostak M, Spain M, Choquette KA, Flowers RA, Procter DJ. Substrate-directable electron transfer reactions. Dramatic rate enhancement in the chemoselective reduction of cyclic esters using SmI2-H 2O: Mechanism, scope, and synthetic utility Journal of the American Chemical Society. 135: 15702-15705. PMID 24079360 DOI: 10.1021/Ja4078864 |
0.475 |
|
2013 |
Szostak M, Spain M, Procter DJ. Recent advances in the chemoselective reduction of functional groups mediated by samarium(II) iodide: a single electron transfer approach. Chemical Society Reviews. 42: 9155-83. PMID 24013846 DOI: 10.1039/C3Cs60223K |
0.438 |
|
2013 |
Sautier B, Collins KD, Procter DJ. Development of an additive-controlled, SmI2-mediated stereoselective sequence: Telescoped spirocyclisation, lactone reduction and Peterson elimination. Beilstein Journal of Organic Chemistry. 9: 1443-7. PMID 23946841 DOI: 10.3762/Bjoc.9.163 |
0.34 |
|
2013 |
Eberhart AJ, Cicoira C, Procter DJ. Nucleophilic ortho -allylation of pyrroles and pyrazoles: An accelerated pummerer/thio-claisen rearrangement sequence Organic Letters. 15: 3994-3997. PMID 23855635 DOI: 10.1021/Ol401786D |
0.418 |
|
2013 |
Szostak M, Spain M, Procter DJ. Uncovering the importance of proton donors in TmI2-promoted electron transfer: Facile C-N bond cleavage in unactivated amides Angewandte Chemie - International Edition. 52: 7237-7241. PMID 23828793 DOI: 10.1002/Anie.201303178 |
0.327 |
|
2013 |
Pinho VD, Procter DJ, Burtoloso ACB. SmI2-mediated couplings of α-amino acid derivatives. Formal synthesis of (-)-pumiliotoxin 251D and (±)-epiquinamide Organic Letters. 15: 2434-2437. PMID 23639065 DOI: 10.1021/Ol400903N |
0.333 |
|
2013 |
Pace V, Rae JP, Harb HY, Procter DJ. NHC-Cu(I) catalysed asymmetric conjugate silyl transfer to unsaturated lactones: application in kinetic resolution. Chemical Communications (Cambridge, England). 49: 5150-2. PMID 23629548 DOI: 10.1039/C3Cc42160K |
0.395 |
|
2013 |
Fazakerley NJ, Helm MD, Procter DJ. Total synthesis of (+)-pleuromutilin Chemistry - a European Journal. 19: 6718-6723. PMID 23589420 DOI: 10.1002/Chem.201300968 |
0.462 |
|
2013 |
Eberhart AJ, Procter DJ. Nucleophilic ortho-propargylation of aryl sulfoxides: An interrupted pummerer/allenyl thio-Claisen rearrangement sequence Angewandte Chemie - International Edition. 52: 4008-4011. PMID 23447131 DOI: 10.1002/Anie.201300223 |
0.312 |
|
2013 |
Fazakerley NJ, Helm MD, Procter DJ. Cover Picture: Total Synthesis of (+)-Pleuromutilin (Chem. Eur. J. 21/2013) Chemistry - a European Journal. 19: 6509-6509. DOI: 10.1002/Chem.201390073 |
0.313 |
|
2012 |
Levick MT, Coote SC, Grace I, Lambert C, Turner ML, Procter DJ. Phase tag-assisted synthesis of benzo[b]carbazole end-capped oligothiophenes. Organic Letters. 14: 5744-7. PMID 23106380 DOI: 10.1021/Ol302748H |
0.751 |
|
2012 |
Szostak M, Procter DJ. Beyond samarium diiodide: vistas in reductive chemistry mediated by lanthanides(II). Angewandte Chemie (International Ed. in English). 51: 9238-56. PMID 22893612 DOI: 10.1002/Anie.201201065 |
0.412 |
|
2012 |
Parmar D, Matsubara H, Price K, Spain M, Procter DJ. Lactone radical cyclizations and cyclization cascades mediated by SmI2-H2O. Journal of the American Chemical Society. 134: 12751-7. PMID 22746316 DOI: 10.1021/Ja3047975 |
0.521 |
|
2012 |
Szostak M, Spain M, Procter DJ. Selective synthesis of 3-hydroxy acids from Meldrum's acids using SmI2-H2O. Nature Protocols. 7: 970-977. PMID 22538848 DOI: 10.1038/Nprot.2012.034 |
0.355 |
|
2012 |
Szostak M, Spain M, Procter DJ. Preparation of samarium(II) iodide: Quantitative evaluation of the effect of water, oxygen, and peroxide content, preparative methods, and the activation of samarium metal Journal of Organic Chemistry. 77: 3049-3059. PMID 22375820 DOI: 10.1021/Jo300135V |
0.361 |
|
2012 |
Szostak M, Collins KD, Fazakerley NJ, Spain M, Procter DJ. A general electron transfer reduction of lactones using SmI 2-H2O Organic and Biomolecular Chemistry. 10: 5820-5824. PMID 22367284 DOI: 10.1039/C2Ob00017B |
0.464 |
|
2012 |
Szostak M, Spain M, Procter DJ. Electron transfer reduction of carboxylic acids using SmI 2-H 2O-Et 3N Organic Letters. 14: 840-843. PMID 22272578 DOI: 10.1021/Ol203361K |
0.409 |
|
2012 |
Sautier B, Lyons SE, Webb MR, Procter DJ. Radical cyclization cascades of unsaturated Meldrum's acid derivatives Organic Letters. 14: 146-149. PMID 22126403 DOI: 10.1021/Ol2029367 |
0.496 |
|
2012 |
Szostak M, Spain M, Parmar D, Procter DJ. Selective reductive transformations using samarium diiodide-water Chemical Communications. 48: 330-346. PMID 21879049 DOI: 10.1039/C1Cc14252F |
0.363 |
|
2012 |
Harb HY, Procter DJ. SmI 2-mediated carbonyl-alkene couplings for the synthesis of small carbocyclic rings Synlett. 6-20. DOI: 10.1055/S-0031-1290093 |
0.354 |
|
2011 |
Eberhart AJ, Imbriglio JE, Procter DJ. Nucleophilic ortho allylation of aryl and heteroaryl sulfoxides Organic Letters. 13: 5882-5885. PMID 21999481 DOI: 10.1021/Ol2025197 |
0.389 |
|
2011 |
Smith LH, Nguyen TT, Sneddon HF, Procter DJ. Synthesis of the ABH rings of ecteinascidin 597 using a connective Pummerer-type cyclisation. Chemical Communications (Cambridge, England). 47: 10821-3. PMID 21863175 DOI: 10.1039/C1Cc13992D |
0.365 |
|
2011 |
Szostak M, Spain M, Procter DJ. Electron transfer reduction of unactivated esters using SmI 2-H 2O Chemical Communications. 47: 10254-10256. PMID 21858308 DOI: 10.1039/C1Cc14014K |
0.376 |
|
2011 |
Szostak M, Procter DJ. Concise syntheses of strychnine and englerin A: The power of reductive cyclizations triggered by samarium iodide Angewandte Chemie - International Edition. 50: 7737-7739. PMID 21780264 DOI: 10.1002/Anie.201103128 |
0.308 |
|
2011 |
Coote SC, Quenum S, Procter DJ. Exploiting Sm(ii) and Sm(iii) in SmI2-initiated reaction cascades: Application in a tag removal-cyclisation approach to spirooxindole scaffolds Organic and Biomolecular Chemistry. 9: 5104-5108. PMID 21617813 DOI: 10.1039/C1Ob05710C |
0.782 |
|
2011 |
Findley TJ, Sucunza D, Miller LC, Helm MD, Helliwell M, Davies DT, Procter DJ. A stereoselective, Sm(II)-mediated approach to decorated cis-hydrindanes: synthetic studies on faurinone and pleuromutilin. Organic & Biomolecular Chemistry. 9: 2433-51. PMID 21327225 DOI: 10.1039/C0Ob01086C |
0.351 |
|
2011 |
Parmar D, Price K, Spain M, Matsubara H, Bradley PA, Procter DJ. Reductive cyclization cascades of lactones using SmI2-H2O. Journal of the American Chemical Society. 133: 2418-20. PMID 21306121 DOI: 10.1021/Ja1114908 |
0.387 |
|
2010 |
Harb HY, Collins KD, Altur JVG, Bowker S, Campbell L, Procter DJ. SmI2-mediated radical cyclizations directed by a C-Si bond Organic Letters. 12: 5446-5449. PMID 21049913 DOI: 10.1021/Ol102278C |
0.418 |
|
2010 |
Sadasivam DV, Teprovich JA, Procter DJ, Flowers RA. Dynamic ligand exchange in reactions of samarium diiodide. Organic Letters. 12: 4140-3. PMID 20722385 DOI: 10.1021/Ol101722C |
0.385 |
|
2010 |
Collins KD, Oliveira JM, Guazzelli G, Sautier B, De Grazia S, Matsubara H, Helliwell M, Procter DJ. Selective reductions of cyclic 1,3-diesters by using SmI2 and H2O Chemistry - a European Journal. 16: 10240-10249. PMID 20645340 DOI: 10.1002/Chem.201000632 |
0.489 |
|
2010 |
Smith LH, Coote SC, Sneddon HF, Procter DJ. Beyond the Pummerer reaction: recent developments in thionium ion chemistry. Angewandte Chemie (International Ed. in English). 49: 5832-44. PMID 20583014 DOI: 10.1002/Anie.201000517 |
0.767 |
|
2010 |
Baker TM, Sloan LA, Choudhury LH, Murai M, Procter DJ. A stereoselective cyclisation cascade mediated by SmI2-H 2O: Synthetic studies towards stolonidiol Tetrahedron Asymmetry. 21: 1246-1261. DOI: 10.1016/J.Tetasy.2010.03.047 |
0.406 |
|
2010 |
Procter DJ, Archer NJ, Needham RA, Bell D, Marchington AP, Rayner CM. ChemInform Abstract: Stereocontrolled Synthesis of Novel Enantiomerically Pure Sulfides and Selenides from (+)-Camphor and (+)-Camphor-10-sulfonyl Chloride. Cheminform. 30: no-no. DOI: 10.1002/chin.199948097 |
0.599 |
|
2010 |
Johnston D, McCusker CM, Procter DJ. ChemInform Abstract: Samarium(II)-Mediated 4-exo trig Ketyl-Olefin Cyclization of Unsaturated Aldehydes. A General, Stereoselective Synthesis of Functionalized Cyclobutanols. Cheminform. 30: no-no. DOI: 10.1002/chin.199936094 |
0.302 |
|
2010 |
PROCTER DJ, THORNTON-PETT M, RAYNER CM. ChemInform Abstract: Discovery, Characterization, and Utilization of Selenoxide-Sulfonic Acid Salts: A New Class of Selenoxide-Based Oxidant and Stable Selenoxide Equivalent. Cheminform. 27: no-no. DOI: 10.1002/chin.199620061 |
0.554 |
|
2010 |
PROCTER DJ, LOVELL SJ, RAYNER CM. ChemInform Abstract: Selenoxide-Sulfonic Acid Adducts: A New System for the Mild, Selective Oxidation of Sulfides to Sulfoxides. Cheminform. 25: no-no. DOI: 10.1002/chin.199435122 |
0.559 |
|
2010 |
PROCTER DJ, RAYNER CM. ChemInform Abstract: Selenoxide-Sulfonic Acid Adducts; a New Class of Stable, Selenoxide- Based Oxidants. Cheminform. 25: no-no. DOI: 10.1002/chin.199428100 |
0.546 |
|
2009 |
Helm MD, Da Silva M, Sucunza D, Findley TJK, Procter DJ. A dialdehyde cyclization cascade: An approach to pleuromutilin Angewandte Chemie - International Edition. 48: 9315-9317. PMID 19902447 DOI: 10.1002/Anie.200905490 |
0.315 |
|
2009 |
Parmar D, Duffy LA, Sadasivam DV, Matsubara H, Bradley PA, Flowers RA, Procter DJ. Studies on the mechanism, selectivity, and synthetic utility of lactone reduction using SmI2 and H2O Journal of the American Chemical Society. 131: 15467-15473. PMID 19764763 DOI: 10.1021/Ja906396U |
0.465 |
|
2009 |
Ovens C, Vogel JC, Martin NG, Procter DJ. Intramolecular aryl transfer to thionium ions in an approach to α-arylacetamides Chemical Communications. 3101-3103. PMID 19462100 DOI: 10.1039/B904577E |
0.341 |
|
2009 |
Guazzelli G, De Grazia S, Collins KD, Matsubara H, Spain M, Procter DJ. Selective reductions of cyclic 1,3-diesters using SmI2 and H2O Journal of the American Chemical Society. 131: 7214-7215. PMID 19422232 DOI: 10.1021/Ja901715D |
0.466 |
|
2009 |
Miller M, Vogel JC, Tsang W, Merrit A, Procter DJ. Formation of N-heterocycles by the reaction of thiols with glyoxamides: Exploring a connective Pummerer-type cyclisation Organic and Biomolecular Chemistry. 7: 589-597. PMID 19156326 DOI: 10.1039/B816608K |
0.414 |
|
2009 |
Helm MD, Sucunza D, Silva MD, Helliwell M, Procter DJ. SmI2-mediated dialdehyde cyclization cascades Tetrahedron Letters. 50: 3224-3226. DOI: 10.1016/J.Tetlet.2009.02.025 |
0.335 |
|
2009 |
Helm MD, Da Silva M, Sucunza D, Helliwell M, Procter DJ. SmI2-mediated dialdehyde 'radical then aldol' cyclization cascades: a feasibility study Tetrahedron. 65: 10816-10829. DOI: 10.1016/J.Tet.2009.09.035 |
0.45 |
|
2008 |
Guazzelli G, Duffy LA, Procter DJ. A Samarium(II)-mediated, stereoselective cyclization for the synthesis of azaspirocycles. Organic Letters. 10: 4291-4. PMID 18767854 DOI: 10.1021/Ol8017209 |
0.419 |
|
2008 |
Shirai A, Miyata O, Tohnai N, Miyata M, Procter DJ, Sucunza D, Naito T. Total synthesis of (-)-martinellic acid via radical addition-cyclization- elimination reaction Journal of Organic Chemistry. 73: 4464-4475. PMID 18473441 DOI: 10.1021/Jo800560P |
0.48 |
|
2008 |
James KM, Willetts N, Procter DJ. Samarium(II) - mediated linker cleavage - cyclization in fluorous synthesis: Reactions of samarium enolates Organic Letters. 10: 1203-1206. PMID 18278933 DOI: 10.1021/Ol800070Y |
0.453 |
|
2008 |
Duffy LA, Matsubara H, Procter DJ. A ring size-selective reduction of lactones using SmI2 and H2O. Journal of the American Chemical Society. 130: 1136-7. PMID 18183982 DOI: 10.1021/Ja078137D |
0.378 |
|
2008 |
Vogel JC, Butler R, Procter DJ. An asymmetric, SmI2-mediated approach to γ-butyrolactones using a new, fluorous-tagged auxiliary Tetrahedron. 64: 11876-11883. DOI: 10.1016/J.Tet.2008.08.110 |
0.341 |
|
2007 |
Miller M, Tsang W, Merritt A, Procter DJ. Exploring a new, connective Pummerer reaction: formation of oxindoles by the reaction of thiols with glyoxamides. Chemical Communications (Cambridge, England). 498-500. PMID 17252107 DOI: 10.1039/B613591A |
0.399 |
|
2007 |
McAllister LA, McCormick RA, James KM, Brand S, Willetts N, Procter DJ. A fluorous, pummerer cyclative-capture strategy for the synthesis of N-heterocycles Chemistry - a European Journal. 13: 1032-1046. PMID 17201006 DOI: 10.1002/Chem.200601429 |
0.381 |
|
2007 |
Sloan LA, Baker TM, Macdonald SJF, Procter DJ. Application of a samarium(II)-mediated spirocyclisation in an asymmetric approach to the cyclopentanol motif of stolonidiol Synlett. 3155-3159. DOI: 10.1055/S-2007-1000821 |
0.38 |
|
2006 |
Sloan LA, Procter DJ. Lanthanide reagents in solid phase synthesis. Chemical Society Reviews. 35: 1221-9. PMID 17225884 DOI: 10.1039/B509215A |
0.341 |
|
2006 |
McAllister LA, Turner KL, Brand S, Stefaniak M, Procter DJ. Solid phase approaches to N-heterocycles using a sulfur linker cleaved by SmI2 Journal of Organic Chemistry. 71: 6497-6507. PMID 16901135 DOI: 10.1021/Jo060940N |
0.423 |
|
2006 |
Turner KL, Baker TM, Islam S, Procter DJ, Stefaniak M. Solid-phase approach to tetrahydroquinolones using a sulfur linker cleaved by SmI2. Organic Letters. 8: 329-32. PMID 16408907 DOI: 10.1021/Ol052730N |
0.398 |
|
2006 |
McCormick RA, James KM, Willetts N, Procter DJ. Developing new cleavage strategies in a fluorous phase pummerer cyclative-capture approach for the synthesis of N-heterocycles Qsar and Combinatorial Science. 25: 709-712. DOI: 10.1002/Qsar.200640050 |
0.374 |
|
2005 |
McKerlie F, Rudkin IM, Wynne G, Procter DJ. Evaluation of a new linker system cleaved using samarium(II) iodide. Application in the solid phase synthesis of carbonyl compounds Organic and Biomolecular Chemistry. 3: 2805-2816. PMID 16032358 DOI: 10.1039/B506294B |
0.384 |
|
2004 |
Kerrigan NJ, Hutchison PC, Heightman TD, Procter DJ. Development of a solid-phase 'asymmetric resin-capture-release' process: Application of an ephedrine chiral resin in an approach to γ- butyrolactonest Organic and Biomolecular Chemistry. 2: 2476-2482. PMID 15326528 DOI: 10.1039/B408836K |
0.373 |
|
2004 |
Edmonds DJ, Johnston D, Procter DJ. Samarium(II)-iodide-mediated cyclizations in natural product synthesis Chemical Reviews. 104: 3371-3403. PMID 15250745 DOI: 10.1021/Cr030017A |
0.408 |
|
2004 |
Hutchison PC, Heightman TD, Procter DJ. Application of A Recyclable Pseudoephedrine Resin in Asymmetric Alkylations on Solid Phase Journal of Organic Chemistry. 69: 790-801. PMID 14750806 DOI: 10.1021/Jo0354950 |
0.379 |
|
2004 |
Kerrigan NJ, Upadhyay T, Procter DJ. The samarium(II)-mediated intermolecular couplings of ketones and β-alkoxyacrylates: A short asymmetric synthesis of an antifungal γ-butyrolactone Tetrahedron Letters. 45: 9087-9090. DOI: 10.1016/J.Tetlet.2004.10.027 |
0.331 |
|
2003 |
Hutton TK, Muir KW, Procter DJ. Switching between novel samarium(II)-mediated cyclizations by a simple change in alcohol cosolvent. Organic Letters. 5: 4811-4. PMID 14653680 DOI: 10.1021/Ol0358399 |
0.307 |
|
2003 |
McAllister LA, Brand S, de Gentile R, Procter DJ. The first Pummerer cyclisations on solid phase. Convenient construction of oxindoles enabled by a sulfur-link to resin. Chemical Communications (Cambridge, England). 2380-1. PMID 14518924 DOI: 10.1039/B307586A |
0.35 |
|
2003 |
Johnston D, Couché E, Edmonds DJ, Muir KW, Procter DJ. The first synthetic studies on pestalotiopsin A. A stereocontrolled approach to the functionalised bicyclic core. Organic & Biomolecular Chemistry. 1: 328-37. PMID 12929428 DOI: 10.1039/B209066J |
0.383 |
|
2003 |
Kerrigan NJ, Hutchison PC, Heightman TD, Procter DJ. Application of an ephedrine chiral linker in a solid-phase, 'asymmetric catch-release' approach to gamma-butyrolactones. Chemical Communications (Cambridge, England). 1402-3. PMID 12841262 DOI: 10.1039/B302471G |
0.314 |
|
2003 |
Edmonds DJ, Muir KW, Procter DJ. The remarkable effect of cosolvent on a samarium(II)-mediated 4-exo-trig cyclization: further synthetic studies on pestalotiopsin A. The Journal of Organic Chemistry. 68: 3190-8. PMID 12688790 DOI: 10.1021/Jo026827O |
0.434 |
|
2002 |
Hutchison PC, Heightman TD, Procter DJ. Evaluation of a pseudoephedrine linker for asymmetric alkylations on solid phase. Organic Letters. 4: 4583-5. PMID 12489935 DOI: 10.1021/Ol0268788 |
0.381 |
|
2002 |
McKerlie F, Procter DJ, Wynne G. Reduction of alpha-aryloxy carbonyl compounds with samarium(II) iodide. A new traceless linker for the solid phase synthesis of carbonyl compounds. Chemical Communications (Cambridge, England). 584-5. PMID 12120134 DOI: 10.1039/B200365C |
0.322 |
|
2002 |
Hutton TK, Muir K, Procter DJ. Samarium(II)-mediated reactions of gamma,delta-unsaturated ketones. Cyclization and fragmentation processes. Organic Letters. 4: 2345-7. PMID 12098243 DOI: 10.1021/Ol0260472 |
0.42 |
|
2001 |
Johnston D, Francon N, Edmonds DJ, Procter DJ. Samarium(II)-mediated 4-exo-trig cyclization. A stereocontrolled approach to the core of pestalotiopsin A. Organic Letters. 3: 2001-4. PMID 11418034 DOI: 10.1021/Ol015976A |
0.353 |
|
2000 |
Procter DJ, Rayner CM. Synthesis of (R)-4,5-Dihydro-3H-Dinaphtho-[2,1-c:1',2'-e]Selenepin Oxide and Preliminary Studies on Its Use in the Oxidation of Sulfides Synthetic Communications. 30: 2975-2987. DOI: 10.1080/00397910008087448 |
0.534 |
|
2000 |
Procter DJ, Rayner CM. Synthesis of (R)-4,5-dihydro-3H-dinaphtho-[2,1-c:1',2'-e]-selenepin oxide and preliminary studies on its use in the oxidation of sulfides Synthetic Communications. 30: 2975-2987. DOI: 10.1080/00397910008087448 |
0.612 |
|
2000 |
Johnston D, McCusker CF, Muir K, Procter DJ. Samarium(II)-mediated 4-exo-trig cyclisations of unsaturated aldehydes. A stereoselective approach to functionalised cyclobutanols Journal of the Chemical Society-Perkin Transactions 1. 681-695. DOI: 10.1039/A909549G |
0.386 |
|
2000 |
Dowsland J, McKerlie F, Procter DJ. Convenient preparation of ytterbium(III) chalcogenolate complexes by insertion of ytterbium into chalcogen-chalcogen bonds. Application in the ring-opening of epoxides Tetrahedron Letters. 41: 4923-4927. DOI: 10.1016/S0040-4039(00)00687-0 |
0.379 |
|
2000 |
Procter DJ, Rayner CM. ChemInform Abstract: Synthesis of (R)-4,5-Dihydro-3H-dinaphtho[2,1-c:1′,2′-e]selenepin Oxide and Preliminary Studies on Its Use in the Oxidation of Sulfides. Cheminform. 31: no-no. DOI: 10.1002/chin.200047057 |
0.545 |
|
1999 |
Procter DJ. The synthesis of thiols, selenols, sulfides, selenides, sulfoxides, selenoxides, sulfones and selenones Journal of the Chemical Society-Perkin Transactions 1. 335-354. DOI: 10.1039/B002081H |
0.328 |
|
1999 |
Johnston D, McCusker CM, Procter DJ. Samarium(II)-mediated 4-exo trig ketyl-olefin cyclisation of unsaturated aldehydes. A general, stereoselective synthesis of functionalised cyclobutanols Tetrahedron Letters. 40: 4913-4916. DOI: 10.1016/S0040-4039(99)00910-7 |
0.434 |
|
1999 |
Procter DJ, Archer NJ, Needham RA, Bell D, Marchington AP, Rayner CM. Stereocontrolled synthesis of novel enantiomerically pure sulfides and selenides from (+)-camphor and (+)-camphor-10-sulfonyl chloride Tetrahedron. 55: 9611-9622. DOI: 10.1016/S0040-4020(99)00507-4 |
0.677 |
|
1998 |
Holton RA, Zhang Z, Clarke PA, Nadizadeh H, Procter DJ. Selective protection of the C(7) and C(10) hydroxyl groups in 10- deacetyl baccatin III Tetrahedron Letters. 39: 2883-2886. DOI: 10.1016/S0040-4039(98)00424-9 |
0.631 |
|
1994 |
Procter DJ, Lovell SJ, Rayner CM. Selenoxide - Sulfonic Acid Adducts: A New System for the Mild, Selective Oxidation of Sulfides to Sulfoxides Synlett. 1994: 204-206. DOI: 10.1055/s-1994-22795 |
0.551 |
|
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