| Year |
Citation |
Score |
| 2023 |
Ali R, Patra T, Wirth T. Alkene reactions with superoxide radical anions in flow electrochemistry. Faraday Discussions. PMID 37475579 DOI: 10.1039/d3fd00050h |
0.695 |
|
| 2022 |
Patra T, Wirth T. Oxidative Cleavage of Alkenes by Photosensitized Nitroarenes. Angewandte Chemie (International Ed. in English). 61: e202213772. PMID 36205628 DOI: 10.1002/anie.202213772 |
0.687 |
|
| 2022 |
Zhang H, Wirth T. Oxidation of BINOLs by Hypervalent Iodine Reagents: Facile Synthesis of Xanthenes and Lactones. Chemistry (Weinheim An Der Bergstrasse, Germany). 28: e202200181. PMID 35225370 DOI: 10.1002/chem.202200181 |
0.331 |
|
| 2021 |
Zhang H, Cormanich RA, Wirth T. Chiral Ligands in Hypervalent Iodine Compounds: Synthesis and Structures of Binaphthyl-based λ3-Iodanes. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 34783401 DOI: 10.1002/chem.202103623 |
0.339 |
|
| 2021 |
Winterson B, Rennigholtz T, Wirth T. Flow electrochemistry: a safe tool for fluorine chemistry. Chemical Science. 12: 9053-9059. PMID 34276934 DOI: 10.1039/d1sc02123k |
0.316 |
|
| 2021 |
Alharbi H, Elsherbini M, Qurban J, Wirth T. C-N Axial Chiral Hypervalent Iodine Reagents: Catalytic Stereose-lective α-Oxytosylation of Ketones. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 33428245 DOI: 10.1002/chem.202005253 |
0.315 |
|
| 2020 |
Huynh F, Tailby M, Finniear A, Stephens K, Allemann RK, Wirth T. Accelerating biphasic biocatalysis through new process windows. Angewandte Chemie (International Ed. in English). PMID 32567753 DOI: 10.1002/Anie.202005183 |
0.404 |
|
| 2020 |
Raynbird MY, Silva F, Smallman H, Khokhar SS, Neef D, Evans GJS, Wirth T. Short Total Synthesis of Ajoene In Batch and an Isomeric Precursor in Continuous Flow. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32364668 DOI: 10.1002/Chem.202001598 |
0.428 |
|
| 2020 |
Elsherbini M, Huynh F, Dunbabin A, Allemann R, Wirth T. Selective hydroboration - oxidation of terminal alkenes under flow conditions. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32329919 DOI: 10.1002/Chem.202001650 |
0.386 |
|
| 2020 |
Wirth T, Hokamp T. Hypervalent Iodine(III)-Catalysed Enantioselective α-Acetoxylation of Ketones. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32233006 DOI: 10.1002/Chem.202000927 |
0.435 |
|
| 2020 |
Gazis TA, Mohajeri Thaker BAJ, Willcox D, Ould DMC, Wenz J, Rawson JM, Hill MS, Wirth T, Melen RL. 1,3-Carboboration of iodonium ylides. Chemical Communications (Cambridge, England). PMID 32090215 DOI: 10.1039/C9Cc08749D |
0.305 |
|
| 2020 |
Amri N, Wirth T. Accelerating Electrochemical Synthesis through Automated Flow: Efficient Synthesis of Chalcogenophosphites Synlett. DOI: 10.1055/S-0040-1707141 |
0.397 |
|
| 2020 |
Amri N, Wirth T. Automated Electrochemical Selenenylations Synthesis. 52: 1751-1761. DOI: 10.1055/S-0039-1690868 |
0.382 |
|
| 2019 |
Elsherbini M, Wirth T. Electroorganic Synthesis under Flow Conditions. Accounts of Chemical Research. PMID 31693339 DOI: 10.1021/Acs.Accounts.9B00497 |
0.401 |
|
| 2019 |
Santi M, Seitz J, Cicala R, Hardwick T, Ahmed N, Wirth T. Memory of Chirality in Flow Electrochemistry: Fast Optimisation with DoE and Online 2D-HPLC. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31692141 DOI: 10.1002/Chem.201904711 |
0.381 |
|
| 2019 |
Allen BDW, Hareram MD, Seastram AC, McBride T, Wirth T, Browne DL, Morrill LC. Manganese-Catalyzed Electrochemical Deconstructive Chlorination of Cycloalkanols via Alkoxy Radicals. Organic Letters. PMID 31687826 DOI: 10.1021/Acs.Orglett.9B03652 |
0.364 |
|
| 2019 |
Gazis TA, Dasgupta A, Hill MS, Rawson JM, Wirth T, Melen RL. Reactions of hydrazones and hydrazides with Lewis acidic boranes. Dalton Transactions (Cambridge, England : 2003). PMID 31397460 DOI: 10.1039/C9Dt01359H |
0.335 |
|
| 2019 |
Qurban J, Elsherbini M, Alharbi H, Wirth T. Synthesis, characterisation, and reactivity of novel pseudocyclic hypervalent iodine reagents with heteroaryl carbonyl substituents. Chemical Communications (Cambridge, England). PMID 31225543 DOI: 10.1039/C9Cc03905H |
0.357 |
|
| 2019 |
Yusubov MS, Soldatova NS, Postnikov PS, Valiev RR, Yoshimura A, Wirth T, Nemykin VN, Zhdankin VV. 2-Iodoxybenzoic acid ditriflate: the most powerful hypervalent iodine(v) oxidant. Chemical Communications (Cambridge, England). PMID 31209449 DOI: 10.1039/C9Cc04203B |
0.311 |
|
| 2019 |
Hokamp T, Wirth T. Structurally Defined α-Tetralol-Based Chiral Hypervalent Iodine Reagents. The Journal of Organic Chemistry. PMID 31179710 DOI: 10.1021/Acs.Joc.9B01315 |
0.401 |
|
| 2019 |
Elsherbini M, Winterson B, Alharbi H, Folgueiras-Amador AA, Génot C, Wirth T. Continuous Electrochemical Generator of Hypervalent Iodine Reagents: Synthetic Applications in Flow. Angewandte Chemie (International Ed. in English). PMID 31050149 DOI: 10.1002/Anie.201904379 |
0.374 |
|
| 2019 |
Santi M, Ould DMC, Wenz J, Soltani Y, Melen RL, Wirth T. Metal-Free Tandem Rearrangement/Lactonization: Access to 3,3-Disubstituted Benzofuran-2-(3H)-ones. Angewandte Chemie (International Ed. in English). PMID 30897253 DOI: 10.1002/Anie.201902985 |
0.38 |
|
| 2019 |
Singh FV, Wirth T. Selenium and Tellurium Electrophiles in Organic Synthesis Physical Sciences Reviews. 4: 131. DOI: 10.1515/Psr-2017-0131 |
0.317 |
|
| 2019 |
Amri N, Skilton RA, Guthrie D, Wirth T. Efficient Flow Electrochemical Alkoxylation of Pyrrolidine-1-carbaldehyde Synlett. 30: 1183-1186. DOI: 10.1055/S-0037-1611774 |
0.435 |
|
| 2019 |
Aldmairi AH, Knight DW, Wirth T. Morpholin-2-one derivatives via intramolecular acid-catalyzed hydroamination Synthesis. 51: 1643-1648. DOI: 10.1055/S-0037-1610674 |
0.413 |
|
| 2019 |
Gao W, Xiong Z, Pirhaghani S, Wirth T. Enantioselective Electrochemical Lactonization Using Chiral Iodoarenes as Mediators Synthesis. 51: 276-284. DOI: 10.1055/S-0037-1610373 |
0.391 |
|
| 2019 |
Singh FV, Wirth T. Selenium reagents as catalysts Catalysis Science & Technology. 9: 1073-1091. DOI: 10.1039/C8Cy02274G |
0.435 |
|
| 2019 |
Soldatova NS, Postnikov PS, Yusubov MS, Wirth T. Flow Synthesis of Iodonium Trifluoroacetates through Direct Oxidation of Iodoarenes by Oxone European Journal of Organic Chemistry. 2019: 2081-2088. DOI: 10.1002/Ejoc.201900220 |
0.372 |
|
| 2019 |
Islam M, Kariuki BM, Shafiq Z, Wirth T, Ahmed N. Efficient Electrosynthesis of Thiazolidin‐2‐imines via Oxysulfurization of Thiourea‐Tethered Terminal Alkenes Using the Flow Microreactor European Journal of Organic Chemistry. 2019: 1371-1376. DOI: 10.1002/Ejoc.201801688 |
0.431 |
|
| 2018 |
Silva F, Khokhar SS, Williams DM, Saunders R, Evans GJS, Graz M, Wirth T. Short Total Synthesis of Ajoene. Angewandte Chemie (International Ed. in English). PMID 30079981 DOI: 10.1002/Anie.201808605 |
0.338 |
|
| 2018 |
Hokamp T, Mollari L, Wilkins LC, Melen RL, Wirth T. Alternative Strategies with Iodine: Fast Access to New Iodine(III) Compounds. Angewandte Chemie (International Ed. in English). PMID 29744994 DOI: 10.1002/Anie.201804642 |
0.45 |
|
| 2018 |
Soldatova N, Postnikov P, Kukurina O, Zhdankin VV, Yoshimura A, Wirth T, Yusubov MS. One-pot synthesis of diaryliodonium salts from arenes and aryl iodides with Oxone-sulfuric acid. Beilstein Journal of Organic Chemistry. 14: 849-855. PMID 29719579 DOI: 10.3762/Bjoc.14.70 |
0.392 |
|
| 2018 |
Elsherbini M, Wirth T. Hypervalent Iodine Reagents by Anodic Oxidation: a Powerful Green Synthesis. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29655209 DOI: 10.1002/Chem.201801232 |
0.364 |
|
| 2018 |
Silva F, Baker A, Stansall J, Michalska W, Yusubov MS, Graz M, Saunders R, Evans GJS, Wirth T. Selective Oxidation of Sulfides in Flow Chemistry European Journal of Organic Chemistry. 2018: 2134-2137. DOI: 10.1002/Ejoc.201800339 |
0.344 |
|
| 2018 |
Yusubov MS, Soldatova NS, Postnikov PS, Valiev RR, Svitich DY, Yusubova RY, Yoshimura A, Wirth T, Zhdankin VV. Reactions of 1‐Arylbenziodoxolones with Azide Anion: Experimental and Computational Study of Substituent Effects European Journal of Organic Chemistry. 2018: 640-647. DOI: 10.1002/Ejoc.201701595 |
0.388 |
|
| 2018 |
Elsherbini M, Wirth T. Frontispiece: Hypervalent Iodine Reagents by Anodic Oxidation: A Powerful Green Synthesis Chemistry: a European Journal. 24. DOI: 10.1002/Chem.201885163 |
0.325 |
|
| 2017 |
Wirth T. Organic synthesis in flow for medicinal chemistry. Bioorganic & Medicinal Chemistry. 25: 6179. PMID 29153554 DOI: 10.1016/J.Bmc.2017.11.013 |
0.321 |
|
| 2017 |
Folgueiras-Amador AA, Qian XY, Xu H, Wirth T. Catalyst- and Supporting Electrolyte-Free Electrosynthesis of Benzothiazoles and Thiazolopyridines in Continuous Flow. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29125202 DOI: 10.1002/Chem.201705016 |
0.404 |
|
| 2017 |
Folgueiras-Amador AA, Philipps K, Guilbaud S, Poelakker J, Wirth T. An Easy-to-Machine Electrochemical Flow Microreactor: Efficient Synthesis of Isoindolinone and Flow Functionalization. Angewandte Chemie (International Ed. in English). 56: 15446-15450. PMID 29045019 DOI: 10.1002/Anie.201709717 |
0.342 |
|
| 2017 |
Qurban J, Elsherbini M, Wirth T. Electron-Deficient Chiral Lactic Acid-Based Hypervalent Iodine Reagents. The Journal of Organic Chemistry. 82: 11872-11876. PMID 28727455 DOI: 10.1021/Acs.Joc.7B01571 |
0.41 |
|
| 2017 |
Tang X, Demiray M, Wirth T, Allemann RK. Concise synthesis of artemisinin from a farnesyl diphosphate analogue. Bioorganic & Medicinal Chemistry. PMID 28404524 DOI: 10.1016/J.Bmc.2017.03.068 |
0.313 |
|
| 2017 |
Demiray M, Tang X, Wirth T, Faraldos JA, Allemann RK. An Efficient Chemoenzymatic Synthesis of Dihydroartemisinic Aldehyde. Angewandte Chemie (International Ed. in English). PMID 28294491 DOI: 10.1002/Anie.201609557 |
0.371 |
|
| 2017 |
Tang X, Allemann RK, Wirth T. Optimising Terpene Synthesis with Flow Biocatalysis. European Journal of Organic Chemistry. 2017: 414-418. PMID 28286413 DOI: 10.1002/Ejoc.201601388 |
0.33 |
|
| 2017 |
Soldatova N, Postnikov P, Kukurina O, Zhdankin VV, Yoshimura A, Wirth T, Yusubov MS. Facile One-Pot Synthesis of Diaryliodonium Salts from Arenes and Aryl Iodides with Oxone. Chemistryopen. 6: 18-20. PMID 28168145 DOI: 10.1002/Open.201600129 |
0.464 |
|
| 2017 |
Wirth T. Novel Organic Synthesis through Ultrafast Chemistry. Angewandte Chemie (International Ed. in English). 56: 682-684. PMID 27891736 DOI: 10.1002/Anie.201609595 |
0.354 |
|
| 2017 |
Aldmairi AH, Knight DW, Wirth T. Acid-Catalyzed Tandem Process for the One-Pot Synthesis of Oxazolidines Synlett. 28: 2976-2978. DOI: 10.1055/S-0036-1591513 |
0.45 |
|
| 2017 |
Hokamp T, Storm AT, Yusubov M, Wirth T. Iodine monoacetate for efficient oxyiodinations of alkenes and alkynes Synlett. 29: 415-418. DOI: 10.1055/S-0036-1589119 |
0.377 |
|
| 2017 |
Elsherbini M, Wirth T. Mechanochemical synthesis of N-tert-butanesulfinyl imines under metal-free conditions Tetrahedron. 74: 3101-3106. DOI: 10.1016/J.Tet.2017.11.028 |
0.324 |
|
| 2017 |
Santi M, Müller STR, Folgueiras‐Amador AA, Uttry A, Hellier P, Wirth T. Enantioselective Synthesis of trans‐2,3‐Dihydro‐1H‐indoles Through C–H Insertion of α‐Diazocarbonyl Compounds European Journal of Organic Chemistry. 2017: 1889-1893. DOI: 10.1002/Ejoc.201700412 |
0.426 |
|
| 2017 |
Malmedy F, Wirth T. Cyclization of malonate derivatives with iodine(III) reagents European Journal of Organic Chemistry. 2017: 786-789. DOI: 10.1002/Ejoc.201601587 |
0.429 |
|
| 2017 |
Wirth T. Neue organische Synthesen durch ultraschnelle Chemie Angewandte Chemie. 129: 698-700. DOI: 10.1002/Ange.201609595 |
0.303 |
|
| 2017 |
Demiray M, Tang X, Wirth T, Faraldos JA, Allemann RK. Effiziente chemoenzymatische Synthese von Dihydroartemisinaldehyd Angewandte Chemie. 129: 4411-4415. DOI: 10.1002/Ange.201609557 |
0.303 |
|
| 2016 |
Malmedy F, Wirth T. Stereoselective Ketone Rearrangements with Hypervalent Iodine Reagents. Chemistry (Weinheim An Der Bergstrasse, Germany). 22: 16072-16077. PMID 27539556 DOI: 10.1002/Chem.201603022 |
0.45 |
|
| 2016 |
Wilkins LC, Günther BA, Walther M, Lawson JR, Wirth T, Melen RL. Contrasting Frustrated Lewis Pair Reactivity with Selenium- and Boron-Based Lewis Acids. Angewandte Chemie (International Ed. in English). PMID 27484052 DOI: 10.1002/Anie.201605239 |
0.352 |
|
| 2016 |
Müller ST, Hokamp T, Ehrmann S, Hellier P, Wirth T. Ethyl Lithiodiazoacetate: Extremely Unstable Intermediate Handled Efficiently in Flow. Chemistry (Weinheim An Der Bergstrasse, Germany). 22: 11940-2. PMID 27339757 DOI: 10.1002/Chem.201602133 |
0.429 |
|
| 2016 |
Brown M, Kumar R, Rehbein J, Wirth T. Enantioselective Oxidative Rearrangements with Chiral Hypervalent Iodine Reagents. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26800241 DOI: 10.1002/Chem.201504844 |
0.393 |
|
| 2016 |
Kumar R, Wirth T. Asymmetric Synthesis with Hypervalent Iodine Reagents. Topics in Current Chemistry. 373: 243-61. PMID 26044514 DOI: 10.1007/128_2015_639 |
0.413 |
|
| 2016 |
Hutchings M, Wirth T. Safe Use of Nitromethane for Aldol Reactions in Flow Journal of Flow Chemistry. 6: 202-205. DOI: 10.1556/1846.2016.00022 |
0.409 |
|
| 2016 |
Mizar P, Wirth T. Iodoaminations of Alkenes Synthesis. 49: 981-986. DOI: 10.1055/S-0036-1588630 |
0.326 |
|
| 2016 |
Hutchings M, Wirth T. A Simple Setup for Transfer Hydrogenations in Flow Chemistry Synlett. DOI: 10.1055/S-0035-1561624 |
0.32 |
|
| 2016 |
Müller STR, Murat A, Hellier P, Wirth T. Toward a Large-Scale Approach to Milnacipran Analogues Using Diazo Compounds in Flow Chemistry Organic Process Research and Development. 20: 495-502. DOI: 10.1021/Acs.Oprd.5B00308 |
0.4 |
|
| 2016 |
Malmedy F, Wirth T. Frontispiece: Stereoselective Ketone Rearrangements with Hypervalent Iodine Reagents Chemistry: a European Journal. 22. DOI: 10.1002/Chem.201684562 |
0.448 |
|
| 2016 |
Brown M, Kumar R, Rehbein J, Wirth T. Back Cover: Enantioselective Oxidative Rearrangements with Chiral Hypervalent Iodine Reagents (Chem. Eur. J. 12/2016) Chemistry: a European Journal. 22: 4296-4296. DOI: 10.1002/Chem.201600402 |
0.372 |
|
| 2015 |
Mizar P, Niebuhr R, Hutchings M, Farooq U, Wirth T. Thioamination of Alkenes with Hypervalent Iodine Reagents. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26660291 DOI: 10.1002/Chem.201504636 |
0.424 |
|
| 2015 |
Tancock J, Wirth T. Selenium-Mediated Synthesis of Tetrasubstituted Naphthalenes through Rearrangement. Molecules (Basel, Switzerland). 20: 10866-72. PMID 26076108 DOI: 10.3390/Molecules200610866 |
0.403 |
|
| 2015 |
Müller ST, Murat A, Maillos D, Lesimple P, Hellier P, Wirth T. Rapid Generation and Safe Use of Carbenes Enabled by a Novel Flow Protocol with In-line IR spectroscopy. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 7016-20. PMID 25808068 DOI: 10.1002/Chem.201500416 |
0.362 |
|
| 2015 |
Baker A, Graz M, Saunders R, Evans GJS, Pitotti I, Wirth T. Flow Alkylation of Thiols, Phenols, and Amines Using a Heterogenous Base in a Packed-Bed Reactor Journal of Flow Chemistry. 5: 65-68. DOI: 10.1556/1846.2015.00009 |
0.409 |
|
| 2015 |
Brown M, Delorme M, Malmedy F, Malmgren J, Olofsson B, Wirth T. Synthesis of New Chiral Diaryliodonium Salts Synlett. 26: 1573-1577. DOI: 10.1055/S-0034-1380687 |
0.425 |
|
| 2014 |
Mizar P, Burrelli A, Günther E, Söftje M, Farooq U, Wirth T. Organocatalytic stereoselective iodoamination of alkenes. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 13113-6. PMID 25156303 DOI: 10.1002/Chem.201404762 |
0.376 |
|
| 2014 |
Mizar P, Laverny A, El-Sherbini M, Farid U, Brown M, Malmedy F, Wirth T. Enantioselective diamination with novel chiral hypervalent iodine catalysts. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 9910-3. PMID 25042733 DOI: 10.1002/Chem.201403891 |
0.399 |
|
| 2014 |
Mizar P, Wirth T. Flexible stereoselective functionalizations of ketones through umpolung with hypervalent iodine reagents. Angewandte Chemie (International Ed. in English). 53: 5993-7. PMID 24846685 DOI: 10.1002/Anie.201400405 |
0.393 |
|
| 2014 |
Arai K, Watts K, Wirth T. Difluoro-and Trifluoromethylation of Electron-Deficient Alkenes in an Electrochemical Microreactor. Chemistryopen. 3: 23-8. PMID 24688891 DOI: 10.1002/Open.201300039 |
0.397 |
|
| 2014 |
Singh FV, Wirth T. Hypervalent iodine-catalyzed oxidative functionalizations including stereoselective reactions. Chemistry, An Asian Journal. 9: 950-71. PMID 24523252 DOI: 10.1002/Asia.201301582 |
0.462 |
|
| 2014 |
Watts K, Baker A, Wirth T. Electrochemical synthesis in microreactors Journal of Flow Chemistry. 4: 2-11. DOI: 10.1556/Jfc-D-13-00030 |
0.336 |
|
| 2014 |
Uchechukwu, Wirth T, Egu SA. Synthesis of Quinolinequinone Derivatives and related Carbocyclic Compounds Scienceopen Research. DOI: 10.14293/S2199-1006.1.Sor-Chem.Aall9P.V1 |
0.402 |
|
| 2014 |
Muller STR, Smith D, Hellier P, Wirth T. Safe generation and direct use of diazoesters in flow chemistry Synlett. 25: 871-875. DOI: 10.1055/S-0033-1340835 |
0.357 |
|
| 2014 |
Arai K, Wirth T. Rapid Electrochemical Deprotection of the Isonicotinyloxycarbonyl Group from Carbonates and Thiocarbonates in a Microfluidic Reactor Organic Process Research & Development. 18: 1377-1381. DOI: 10.1021/Op500155F |
0.339 |
|
| 2014 |
Elsherbini M, Hamama WS, Zoorob HH, Bhowmick D, Mugesh G, Wirth T. Synthesis and Antioxidant Activities of Novel Chiral Ebselen Analogues Heteroatom Chemistry. 25: 320-325. DOI: 10.1002/Hc.21164 |
0.382 |
|
| 2014 |
Ambreen N, Wirth T. High-Temperature Synthesis of Amides from Alcohols or Aldehydes by Using Flow Chemistry European Journal of Organic Chemistry. 2014: 7590-7593. DOI: 10.1002/Ejoc.201403280 |
0.393 |
|
| 2013 |
Ambreen N, Kumar R, Wirth T. Hypervalent iodine/TEMPO-mediated oxidation in flow systems: a fast and efficient protocol for alcohol oxidation. Beilstein Journal of Organic Chemistry. 9: 1437-42. PMID 23946840 DOI: 10.3762/Bjoc.9.162 |
0.346 |
|
| 2013 |
Farid U, Malmedy F, Claveau R, Albers L, Wirth T. Stereoselective rearrangements with chiral hypervalent iodine reagents. Angewandte Chemie (International Ed. in English). 52: 7018-22. PMID 23653165 DOI: 10.1002/Anie.201302358 |
0.417 |
|
| 2013 |
Baker A, Graz M, Saunders R, Evans GJS, Kaul S, Wirth T. Flow synthesis of symmetrical di- and trisulfides using phase-transfer catalysis Journal of Flow Chemistry. 3: 118-121. DOI: 10.1556/Jfc-D-13-00013 |
0.405 |
|
| 2013 |
Singh FV, Wirth T. Oxidative rearrangements with hypervalent iodine reagents Synthesis. 45: 2499-2511. DOI: 10.1055/S-0033-1339679 |
0.417 |
|
| 2013 |
Brown M, Farid U, Wirth T. Hypervalent iodine reagents as powerful electrophiles Synlett. 24: 424-431. DOI: 10.1055/S-0032-1318103 |
0.389 |
|
| 2013 |
König B, Kreitmeier P, Hilgers P, Wirth T. Flow Chemistry in Undergraduate Organic Chemistry Education Journal of Chemical Education. 90: 934-936. DOI: 10.1021/Ed3006083 |
0.322 |
|
| 2013 |
Farid U, Malmedy F, Claveau R, Albers L, Wirth T. Inside Cover: Stereoselective Rearrangements with Chiral Hypervalent Iodine Reagents (Angew. Chem. Int. Ed. 27/2013) Angewandte Chemie. 52: 6788-6788. DOI: 10.1002/Anie.201304229 |
0.368 |
|
| 2013 |
Farid U, Malmedy F, Claveau R, Albers L, Wirth T. Stereoselective rearrangements with chiral hypervalent iodine reagents Angewandte Chemie - International Edition. 52: 7018-7022. DOI: 10.1002/anie.201302358 |
0.307 |
|
| 2012 |
Singh FV, Rehbein J, Wirth T. Facile oxidative rearrangements using hypervalent iodine reagents. Chemistryopen. 1: 245-50. PMID 24551514 DOI: 10.1002/Open.201200037 |
0.47 |
|
| 2012 |
Farid U, Wirth T. Highly stereoselective metal-free oxyaminations using chiral hypervalent iodine reagents. Angewandte Chemie (International Ed. in English). 51: 3462-5. PMID 22278888 DOI: 10.1002/Anie.201107703 |
0.367 |
|
| 2012 |
Audiger L, Watts K, Elmore SC, Robinson RI, Wirth T. Ritter reactions in flow. Chemsuschem. 5: 257-60. PMID 22135007 DOI: 10.1002/Cssc.201100372 |
0.388 |
|
| 2012 |
Singh FV, Wirth T. Hypervalent iodine mediated oxidative cyclization of o-hydroxystilbenes into benzo- and naphthofurans Synthesis. 44: 1171-1177. DOI: 10.1055/S-0031-1290588 |
0.379 |
|
| 2012 |
Santi C, Di Lorenzo R, Tidei C, Bagnoli L, Wirth T. Stereoselective selenium catalyzed dihydroxylation and hydroxymethoxylation of alkenes Tetrahedron. 68: 10530-10535. DOI: 10.1016/J.Tet.2012.08.078 |
0.78 |
|
| 2012 |
Gabriele E, Singh FV, Freudendahl DM, Wirth T. Selenenylations of alkenes with styrene nucleophiles Tetrahedron. 68: 10573-10576. DOI: 10.1016/J.Tet.2012.08.034 |
0.426 |
|
| 2012 |
Farid U, Wirth T. Inside Back Cover: Highly Stereoselective Metal-Free Oxyaminations Using Chiral Hypervalent Iodine Reagents (Angew. Chem. Int. Ed. 14/2012) Angewandte Chemie. 51: 3491-3491. DOI: 10.1002/Anie.201201230 |
0.37 |
|
| 2011 |
Singh FV, Wirth T. Selenium-catalyzed regioselective cyclization of unsaturated carboxylic acids using hypervalent iodine oxidants. Organic Letters. 13: 6504-7. PMID 22085140 DOI: 10.1021/Ol202800K |
0.434 |
|
| 2011 |
Watts K, Gattrell W, Wirth T. A practical microreactor for electrochemistry in flow. Beilstein Journal of Organic Chemistry. 7: 1108-14. PMID 21915214 DOI: 10.3762/Bjoc.7.127 |
0.383 |
|
| 2011 |
Ahmed-Omer B, Barrow DA, Wirth T. Multistep reactions using microreactor chemistry Arkivoc. 2011. DOI: 10.3998/Ark.5550190.0012.404 |
0.43 |
|
| 2011 |
Wang XJ, Frutos RP, Zhang L, Sun X, Xu Y, Wirth T, Nicola T, Nummy LJ, Krishnamurthy D, Busacca CA, Yee N, Senanayake CH. Asymmetric synthesis of LFA-1 inhibitor BIRT2584 on metric ton scale Organic Process Research and Development. 15: 1185-1191. DOI: 10.1021/Op200175T |
0.365 |
|
| 2011 |
Zhao L, Li Z, Wirth T. Asymmetric Methoxyselenenylations with Chiral Selenium Electrophiles European Journal of Organic Chemistry. 2011: 7080-7082. DOI: 10.1002/Ejoc.201101373 |
0.416 |
|
| 2011 |
Zhao L, Li Z, Wirth T. Preparation of Novel Chiral Non-Racemic Diselenides and Applications in Asymmetric Synthesis European Journal of Organic Chemistry. 2011: 176-182. DOI: 10.1002/Ejoc.201001272 |
0.432 |
|
| 2011 |
Singh FV, Wirth T. Stereoselective Reactions of Organoselenium Reagents Including Catalysis Patai's Chemistry of Functional Groups. DOI: 10.1002/9780470682531.Pat0573 |
0.453 |
|
| 2010 |
Wang XJ, Xu Y, Zhang L, Krishnamurthy D, Wirth T, Nicola T, Senanayake CH. Efficient synthesis of a small molecule, nonpeptide inhibitor of LFA-1. Organic Letters. 12: 4412-5. PMID 20831178 DOI: 10.1021/Ol101960X |
0.36 |
|
| 2010 |
Schäfer S, Wirth T. A versatile and highly reactive polyfluorinated hypervalent iodine(III) compound. Angewandte Chemie (International Ed. in English). 49: 2786-9. PMID 20235257 DOI: 10.1002/Anie.200907134 |
0.368 |
|
| 2010 |
Shahzad SA, Vivant C, Wirth T. Selenium-mediated synthesis of biaryls through rearrangement. Organic Letters. 12: 1364-7. PMID 20178316 DOI: 10.1021/Ol100274E |
0.434 |
|
| 2010 |
Zhao L, Li Z, Wirth T. Triptycene Derivatives: Synthesis and Applications Chemistry Letters. 39: 658-667. DOI: 10.1246/Cl.2010.658 |
0.332 |
|
| 2010 |
Brandt JC, Elmore SC, Robinson RI, Wirth T. Safe and efficient ritter reactions in flow Synlett. 3099-3103. DOI: 10.1055/S-0030-1259075 |
0.412 |
|
| 2010 |
Farooq U, Schäfer S, Shah AA, Freudendahl DM, Wirth T. Synthesis of New EnantiomericallyPure Organoiodine Catalysts and Their Application in the α-Functionalizationof Ketones Synthesis. 2010: 1023-1029. DOI: 10.1055/S-0029-1218640 |
0.417 |
|
| 2010 |
Altermann SM, Schäfer S, Wirth T. New chiral hypervalent iodine(V) compounds as stoichiometric oxidants Tetrahedron. 66: 5902-5907. DOI: 10.1016/J.Tet.2010.05.079 |
0.373 |
|
| 2010 |
Khan ZA, Iwaoka M, Wirth T. Novel cyclization cascades to functionalized indanes and tetrahydronaphthalenes Tetrahedron. 66: 6639-6646. DOI: 10.1016/J.Tet.2010.03.062 |
0.333 |
|
| 2010 |
Freudendahl DM, Iwaoka M, Wirth T. Synthesis of New Sulfoxide-Containing Diselenides and Unexpected Cyclization Reactions to 2,3-Dihydro-1,4-benzoselenothiine 1-Oxides European Journal of Organic Chemistry. 2010: 3934-3944. DOI: 10.1002/Ejoc.201000514 |
0.467 |
|
| 2010 |
Shahzad SA, Venin C, Wirth T. Diselenide- and Disulfide-Mediated Synthesis of Isocoumarins European Journal of Organic Chemistry. 2010: 3465-3472. DOI: 10.1002/Ejoc.201000308 |
0.429 |
|
| 2009 |
Freudendahl DM, Santoro S, Shahzad SA, Santi C, Wirth T. Green chemistry with selenium reagents: development of efficient catalytic reactions. Angewandte Chemie (International Ed. in English). 48: 8409-11. PMID 19802863 DOI: 10.1002/Anie.200903893 |
0.745 |
|
| 2009 |
Shah AU, Khan ZA, Choudhary N, Lohölter C, Schäfer S, Marie GP, Farooq U, Witulski B, Wirth T. Iodoxolone-based hypervalent iodine reagents. Organic Letters. 11: 3578-81. PMID 19610610 DOI: 10.1021/Ol9014688 |
0.422 |
|
| 2009 |
Brandt JC, Wirth T. Controlling hazardous chemicals in microreactors: synthesis with iodine azide. Beilstein Journal of Organic Chemistry. 5: 30. PMID 19590743 DOI: 10.3762/Bjoc.5.30 |
0.44 |
|
| 2009 |
Shahzad SA, Wirth T. Fast synthesis of benzofluorenes by selenium-mediated carbocyclizations. Angewandte Chemie (International Ed. in English). 48: 2588-91. PMID 19241429 DOI: 10.1002/Anie.200806148 |
0.33 |
|
| 2009 |
Farooq U, Shah AU, Wirth T. Hypervalent bromine compounds: smaller, more reactive analogues of hypervalent iodine compounds. Angewandte Chemie (International Ed. in English). 48: 1018-20. PMID 19117007 DOI: 10.1002/Anie.200805027 |
0.305 |
|
| 2009 |
Khan ZA, Wirth T. Synthesis of indene derivatives via electrophilic cyclization Organic Letters. 11: 229-231. PMID 19049395 DOI: 10.1021/Ol8024956 |
0.437 |
|
| 2009 |
Uehlin L, Wirth T. Synthesis of Chiral Acetals by Asymmetric Selenenylations Phosphorus Sulfur and Silicon and the Related Elements. 184: 1374-1385. DOI: 10.1080/10426500902930167 |
0.394 |
|
| 2009 |
Ahmed-Omer B, Barrow DA, Wirth T. Heck reactions using segmented flow conditions Tetrahedron Letters. 50: 3352-3355. DOI: 10.1016/J.Tetlet.2009.02.133 |
0.389 |
|
| 2009 |
Freudendahl D, Santoro S, Shahzad S, Santi C, Wirth T. Grüne Chemie mit Selenreagentien: Entwicklung effizienter katalytischer Reaktionen Angewandte Chemie. 121: 8559-8562. DOI: 10.1002/Ange.200903893 |
0.68 |
|
| 2009 |
Shahzad SA, Wirth T. Schnelle Synthese von Benzofluorenen durch selenvermittelte Carbocyclisierungen Angewandte Chemie. 121: 2626-2628. DOI: 10.1002/Ange.200806148 |
0.329 |
|
| 2008 |
Browne DM, Niyomura O, Wirth T. Catalytic Addition-Elimination Reactions Towards Butenolides Phosphorus Sulfur and Silicon and the Related Elements. 183: 1026-1035. DOI: 10.1080/10426500801901053 |
0.419 |
|
| 2008 |
Ahmed-Omer B, Barrow DA, Wirth T. Effect of segmented fluid flow, sonication and phase transfer catalysis on biphasic reactions in capillary microreactors Chemical Engineering Journal. 135. DOI: 10.1016/J.Cej.2007.07.017 |
0.348 |
|
| 2008 |
Altermann SM, Richardson RD, Page TK, Schmidt RK, Holland E, Mohammed U, Paradine SM, French AN, Richter C, Bahar AM, Witulski B, Wirth T. Catalytic enantioselective α-oxysulfonylation of ketones mediated by iodoarenes European Journal of Organic Chemistry. 5315-5328. DOI: 10.1002/Ejoc.200800741 |
0.452 |
|
| 2007 |
Richardson RD, Zayed JM, Altermann S, Smith D, Wirth T. Tetrafluoro-IBA and-IBX: hypervalent iodine reagents. Angewandte Chemie (International Ed. in English). 46: 6529-32. PMID 17645277 DOI: 10.1002/Anie.200702313 |
0.444 |
|
| 2007 |
Browne DM, Niyomura O, Wirth T. Catalytic use of selenium electrophiles in cyclizations. Organic Letters. 9: 3169-71. PMID 17608489 DOI: 10.1021/Ol071223Y |
0.446 |
|
| 2007 |
Richardson RD, Desaize M, Wirth T. Hypervalent iodine-mediated aziridination of alkenes: mechanistic insights and requirements for catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). 13: 6745-54. PMID 17514676 DOI: 10.1002/Chem.200700306 |
0.428 |
|
| 2007 |
Bürgler FW, Fragale G, Wirth T. Stereoselective addition reactions with chalcogen electrophiles Arkivoc. 2007. DOI: 10.3998/Ark.5550190.0008.A04 |
0.458 |
|
| 2007 |
Richardson RD, Page TK, Altermann S, Paradine SM, French AN, Wirth T. Enantioselective α-oxytosylation of ketones catalysed by iodoarenes Synlett. 538-542. DOI: 10.1055/S-2007-967960 |
0.452 |
|
| 2007 |
Ahmed-Omer B, Brandt JC, Wirth T. Advanced organic synthesis using microreactor technology Organic and Biomolecular Chemistry. 5: 733-740. DOI: 10.1039/B615072A |
0.356 |
|
| 2006 |
Richardson RD, Wirth T. Hypervalent iodine goes catalytic. Angewandte Chemie (International Ed. in English). 45: 4402-4. PMID 16804953 DOI: 10.1002/Anie.200601817 |
0.335 |
|
| 2006 |
Yusubov MS, Wirth T. Solvent-free reactions with hypervalent iodine reagents. Organic Letters. 7: 519-21. PMID 15673279 DOI: 10.1021/Ol047363E |
0.423 |
|
| 2006 |
Page TK, Wirth T. Simple Direct Synthesis of [Bis(trifluoroacetoxy)iodo]arenes Synthesis. 2006: 3153-3155. DOI: 10.1055/S-2006-942543 |
0.359 |
|
| 2006 |
Ahmed B, Barrow DA, Wirth T. Enhancement of Reaction Rates by Segmented Fluid Flow in Capillary Scale Reactors Advanced Synthesis & Catalysis. 348: 1043-1048. DOI: 10.1002/Adsc.200505480 |
0.368 |
|
| 2005 |
Haas J, Bissmire S, Wirth T. Iodine monochloride-amine complexes: an experimental and computational approach to new chiral electrophiles. Chemistry: a European Journal. 11: 5777-5785. PMID 16038008 DOI: 10.1002/Chem.200500507 |
0.367 |
|
| 2005 |
Wirth T. Hypervalent iodine chemistry in synthesis: scope and new directions. Angewandte Chemie. 44: 3656-3665. PMID 15828037 DOI: 10.1002/Anie.200500115 |
0.387 |
|
| 2005 |
Wirth T, Cox M. Synthesis of a Selenium-Substituted Diselenide Phosphorus Sulfur and Silicon and the Related Elements. 180: 659-666. DOI: 10.1080/10426500590907282 |
0.464 |
|
| 2005 |
Khokhar SS, Wirth T. Control of Selenocyclisations Phosphorus Sulfur and Silicon and the Related Elements. 180: 1087-1098. DOI: 10.1080/10426500590904816 |
0.407 |
|
| 2005 |
Montoro R, Wirth T. Direct Bromination and Iodination of Non-Activated Alkanes by Hypohalite Reagents Synthesis. 2005: 1473-1478. DOI: 10.1055/S-2005-865322 |
0.381 |
|
| 2005 |
Pastor A, Adam W, Wirth T, Tóth G. Diastereoselective Reactions of the Tiglic Acid Functionality Mediated by Oxazolidine Chiral Auxiliaries: A Mechanistic Comparison of DMD andm-CPBA Epoxidations versus Singlet Oxygen and PTAD Ene Reactions European Journal of Organic Chemistry. 2005: 3075-3084. DOI: 10.1002/Ejoc.200500077 |
0.404 |
|
| 2005 |
Arrica MA, Wirth T. Fluorinations of α‐Seleno Carboxylic Acid Derivatives with Hypervalent (Difluoroiodo)toluene European Journal of Organic Chemistry. 2005: 395-403. DOI: 10.1002/Ejoc.200400659 |
0.446 |
|
| 2005 |
Wirth T. Hypervalente Iodverbindungen in der Synthese: Möglichkeiten und Grenzen Angewandte Chemie. 117: 3722-3731. DOI: 10.1002/Ange.200500115 |
0.33 |
|
| 2004 |
Nardello V, Caron L, Aubry JM, Bouttemy S, Wirth T, Saha-Möller Chantu R, Adam W. Reactivity, chemoselectivity, and diastereoselectivity of the oxyfunctionalization of chiral allylic alcohols and derivatives in microemulsions: comparison of the chemical oxidation by the hydrogen peroxide/sodium molybdate system with the photooxygenation. Journal of the American Chemical Society. 126: 10692-700. PMID 15327328 DOI: 10.1021/Ja048589F |
0.387 |
|
| 2004 |
French AN, Bissmire S, Wirth T. Iodine electrophiles in stereoselective reactions: recent developments and synthetic applications Chemical Society Reviews. 33: 354-362. PMID 15280968 DOI: 10.1039/B310389G |
0.424 |
|
| 2004 |
Montoro R, Wirth T. Direct iodination of alkanes. Organic Letters. 5: 4729-31. PMID 14627426 DOI: 10.1021/Ol0359012 |
0.36 |
|
| 2004 |
French AN, Cole J, Wirth T. Tetrahydrofuranylation of alcohols using hypervalent iodine reagents Synlett. 2004: 2291-2294. DOI: 10.1055/S-2004-832810 |
0.324 |
|
| 2004 |
Khokhar SS, Wirth T. Nucleophile-selective selenocyclizations European Journal of Organic Chemistry. 4567-4581. DOI: 10.1002/Ejoc.200400526 |
0.435 |
|
| 2004 |
Khokhar SS, Wirth T. Selenocyclizations: Control by Coordination and by the Counterion Angewandte Chemie - International Edition. 43: 631-633. DOI: 10.1002/Anie.200352884 |
0.368 |
|
| 2003 |
Boye AC, Meyer D, Ingison CK, French AN, Wirth T. Novel lactonization with phenonium ion participation induced by hypervalent iodine reagents. Organic Letters. 5: 2157-9. PMID 12790553 DOI: 10.1021/Ol034616F |
0.318 |
|
| 2003 |
Biland AS, Altermann S, Wirth T. Cyclopropanation of alkenes using hypervalent iodine reagents Arkivoc. 2003. DOI: 10.3998/Ark.5550190.0004.618 |
0.442 |
|
| 2003 |
Wirth T. Oxidations and rearrangements Topics in Current Chemistry. 224: 185-208. DOI: 10.1007/3-540-46114-0_7 |
0.358 |
|
| 2003 |
Wirth T. “New” Reagents for the “Lold” Pinacol Coupling Reaction Organic Synthesis Set. 113-118. DOI: 10.1002/9783527620784.Ch20B |
0.367 |
|
| 2003 |
Wirth T. IBX—New Reactions with an Old Reagent Organic Synthesis Set. 144-150. DOI: 10.1002/9783527620784.Ch15D |
0.378 |
|
| 2002 |
Uehlin L, Fragale G, Wirth T. New and efficient chiral selenium electrophiles Chemistry: a European Journal. 8: 1125-1133. PMID 11891900 DOI: 10.1002/1521-3765(20020301)8:5<1125::Aid-Chem1125>3.0.Co;2-I |
0.441 |
|
| 2002 |
Haas J, Piguel S, Wirth T. Reagent-controlled stereoselective iodolactonizations. Organic Letters. 4: 297-300. PMID 11796074 DOI: 10.1021/Ol0171113 |
0.372 |
|
| 2001 |
Uehlin L, Wirth T. Novel Polymer-Bound Chiral Selenium Electrophiles Organic Letters. 3: 2931-2933. PMID 11529793 DOI: 10.1021/Ol0164435 |
0.354 |
|
| 2001 |
Wirth T. IBX-New Reactions with an Old Reagent. Angewandte Chemie. 40: 2812-2814. PMID 11500874 DOI: 10.1002/1521-3773(20010803)40:15<2812::Aid-Anie2812>3.0.Co;2-X |
0.415 |
|
| 2001 |
Uehlin L, Wirth T. Mixed Acetals as New Precursors for Selenium Electrophiles Phosphorus Sulfur and Silicon and the Related Elements. 172: 189-194. DOI: 10.1080/10426500108046650 |
0.439 |
|
| 2001 |
Hirt UH, Schuster MFH, French AN, Wiest OG, Wirth T. Chiral hypervalent organo-iodine(III) compounds European Journal of Organic Chemistry. 1569-1579. DOI: 10.1002/1099-0690(200104)2001:8<1569::Aid-Ejoc1569>3.0.Co;2-T |
0.462 |
|
| 2000 |
Wirth T. Organoselenium Chemistry in Stereoselective Reactions. Angewandte Chemie. 39: 3740-3749. PMID 11091451 DOI: 10.1002/1521-3773(20001103)39:21<3740::Aid-Anie3740>3.0.Co;2-N |
0.447 |
|
| 2000 |
Adam W, Pastor A, Wirth T. Direct amination of olefins through sequential triazolinedione ene reaction and carbanion-assisted cleavage of the N-N urazole bond Organic Letters. 2: 1295-7. PMID 10810731 DOI: 10.1021/Ol000044C |
0.347 |
|
| 2000 |
Wirth T. Oxygen and Osmium-A New Alliance for Dihydroxylations? Angewandte Chemie. 39: 334-335. PMID 10649400 DOI: 10.1002/(Sici)1521-3773(20000117)39:2<334::Aid-Anie334>3.0.Co;2-5 |
0.336 |
|
| 2000 |
Spichty M, Fragale G, Wirth T. Theoretical investigations on the stereoselective selenenylation reaction of alkenes Journal of the American Chemical Society. 122: 10914-10916. DOI: 10.1021/Ja001602L |
0.4 |
|
| 2000 |
Wirth T. Organoselenchemie in der stereoselektiven Synthese Angewandte Chemie. 112: 3890-3900. DOI: 10.1002/1521-3757(20001103)112:21<3890::Aid-Ange3890>3.0.Co;2-L |
0.33 |
|
| 1999 |
Santi C, Wirth T. Synthesis of non-racemic nitrogen-containing diselenides as efficient precursor catalysts in the diethylzinc addition to benzaldehyde Tetrahedron: Asymmetry. 10: 1019-1023. DOI: 10.1016/S0957-4166(99)00090-7 |
0.612 |
|
| 1999 |
Wirth T. Chiral selenium compounds in organic synthesis Tetrahedron. 55: 1-28. DOI: 10.1016/S0040-4020(98)00946-6 |
0.343 |
|
| 1998 |
Wirth T. Stereoselection at the Steady State: The Design of New Asymmetric Reactions. Angewandte Chemie (International Ed. in English). 37: 2069-2071. PMID 29711065 DOI: 10.1002/(Sici)1521-3773(19980817)37:15<2069::Aid-Anie2069>3.0.Co;2-# |
0.441 |
|
| 1998 |
Wirth T. Asymmetric Synthesis with Chiral Diselenides Phosphorus Sulfur and Silicon and the Related Elements. 136: 235-238. DOI: 10.1080/10426509808545948 |
0.359 |
|
| 1998 |
Wirth T, Fragale G. Stereoselective Isoquinoline Alkaloid Synthesis With New Diselenides Synthesis. 1998: 162-166. DOI: 10.1055/S-1998-2011 |
0.371 |
|
| 1998 |
Fragale G, Wirth T, Neuburger M. New and efficient selenium reagents for stereoselective selenenylation reactions Chemical Communications. 1867-1868. DOI: 10.1039/A804264K |
0.448 |
|
| 1998 |
Hirt UH, Spingler B, Wirth T. New chiral hypervalent iodine compounds in asymmetric synthesis Journal of Organic Chemistry. 63: 7674-7679. DOI: 10.1021/Jo980475X |
0.444 |
|
| 1998 |
Adam W, Renze J, Wirth T. Stereoelectronic Control Of The Diastereoselectivity In The Photooxygenation (Schenck Ene Reaction) Of An Electron-Poor Allylic Alcohol And Its Ethers Journal of Organic Chemistry. 63: 226-227. DOI: 10.1021/Jo971963S |
0.325 |
|
| 1998 |
Adam W, Güthlein M, Peters E-, Peters K, Wirth T. Chiral-Auxiliary-Induced Diastereoselectivity in the [4 + 2] Cycloadditions of Optically Active 2,2-Dimethyloxazolidine Derivatives of Sorbic Acid: A Model Study with Singlet Oxygen as the Smallest Dienophile Journal of the American Chemical Society. 120: 4091-4093. DOI: 10.1021/Ja980059U |
0.31 |
|
| 1998 |
Wirth T, Fragale G, Spichty M. Mechanistic Course of the Asymmetric Methoxyselenenylation Reaction Journal of the American Chemical Society. 120: 3376-3381. DOI: 10.1021/Ja974177D |
0.347 |
|
| 1998 |
Santi C, Fragale G, Wirth T. Synthesis Of A New Chiral Nitrogen Containing Diselenide As A Precursor For Selenium Electrophiles Tetrahedron-Asymmetry. 9: 3625-3628. DOI: 10.1016/S0957-4166(98)00380-2 |
0.618 |
|
| 1998 |
Wirth T, Häuptli S, Leuenberger M. Catalytic asymmetric oxyselenenylation–elimination reactions using chiral selenium compounds Tetrahedron: Asymmetry. 9: 547-550. DOI: 10.1016/S0957-4166(98)00031-7 |
0.449 |
|
| 1998 |
Adam W, Nestler B, Pastor A, Wirth T. Hydroxy-directed diastereoselective ene reaction of triazolinediones with chiral allylic alcohols Tetrahedron Letters. 39: 2625-2628. DOI: 10.1016/S0040-4039(98)00222-6 |
0.392 |
|
| 1998 |
Fragale G, Wirth T. Chiral Diselenides in Asymmetric Cyclization Reactions European Journal of Organic Chemistry. 1998: 1361-1369. DOI: 10.1002/(Sici)1099-0690(199807)1998:7<1361::Aid-Ejoc1361>3.0.Co;2-M |
0.441 |
|
| 1998 |
Adam W, Wirth T, Pastor A, Peters K. Dramatic Diastereoselectivity Differences in the Asymmetric Ene Reactions of Triazolinediones and Singlet Oxygen with Chiral 2,2-Dimethyloxazolidine Derivatives of Tiglic Acid European Journal of Organic Chemistry. 1998: 501-506. DOI: 10.1002/(Sici)1099-0690(199803)1998:3<501::Aid-Ejoc501>3.0.Co;2-Q |
0.4 |
|
| 1997 |
Wirth T, Hirt UH. Chiral hypervalent iodine compounds Tetrahedron-Asymmetry. 8: 23-26. DOI: 10.1016/S0957-4166(96)00469-7 |
0.412 |
|
| 1997 |
Wirth T. Chiral Selenium Compounds: Versatile Reagents In Organic Synthesis Liebigs Annalen. 1997: 2189-2196. DOI: 10.1002/Jlac.199719971104 |
0.453 |
|
| 1997 |
Wirth T. First Total Synthesis of (+)-Membrine Liebigs Annalen. 1997: 1155-1158. DOI: 10.1002/Jlac.199719970616 |
0.43 |
|
| 1997 |
Wirth T, Fragale G. Asymmetric Addition Reactions with Optimized Selenium Electrophiles Chemistry: a European Journal. 3: 1894-1902. DOI: 10.1002/Chem.19970031123 |
0.431 |
|
| 1996 |
Wirth T, Kulicke KJ, Fragale G. Chiral Diselenides in the Total Synthesis of (+)-Samin Journal of Organic Chemistry. 61: 2686-2689. PMID 11667098 DOI: 10.1021/Jo952093M |
0.47 |
|
| 1996 |
Wirth T, Kulicke KJ, Fragale G. Chiral Diselenides from Benzylamines: Catalysts in the Diethylzinc Addition to Aldehydes Helvetica Chimica Acta. 79: 1957-1966. DOI: 10.1002/Hlca.19960790718 |
0.363 |
|
| 1996 |
Wirth T. “New” Reagents for the “Old” Pinacol Coupling Reaction Angewandte Chemie. 35: 61-63. DOI: 10.1002/Anie.199600611 |
0.367 |
|
| 1995 |
Blechert S, Knier R, Schroers H, Wirth T. Domino Reactions - New Concepts in the Synthesis of Indole Alkaloids and Other Polycyclic Indole Derivatives Synthesis. 1995: 592-604. DOI: 10.1055/S-1995-3950 |
0.608 |
|
| 1995 |
Wirth T. Enantioselective alkylation of aldehydes catalyzed by new chiral diselenides Tetrahedron Letters. 36: 7849-7852. DOI: 10.1016/0040-4039(95)01668-8 |
0.394 |
|
| 1995 |
Wirth T. Asymmetric Reaction of Arylalkenes with Diselenides Angewandte Chemie. 34: 1726-1728. DOI: 10.1002/Anie.199517261 |
0.399 |
|
| 1994 |
Wirth T, Blechert S. Synthesis of 2,3-Disubstituted Indoles Synlett. 1994: 717-718. DOI: 10.1055/S-1994-22982 |
0.57 |
|
| 1994 |
Kawabata T, Wirth T, Yahiro K, Suzuki H, Fuji K. Direct Asymmetric .alpha.-Alkylation of Phenylalanine Derivatives Using No External Chiral Sources Journal of the American Chemical Society. 116: 10809-10810. DOI: 10.1021/Ja00102A066 |
0.501 |
|
| 1992 |
Blechert S, Wirth T. Proton-induced Diels-Alder reactions of 2-Vinylindoles Tetrahedron Letters. 33: 6621-6624. DOI: 10.1016/S0040-4039(00)61001-8 |
0.595 |
|
| 1991 |
Blechert S, Wirth T. Nucleophilic additions to acceptor-substituted 2-vinylindoles Tetrahedron Letters. 32: 7237-7240. DOI: 10.1016/0040-4039(91)80485-O |
0.566 |
|
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