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Tobias Ritter - Publications

Affiliations: 
2006-2015 Chemistry and Chemical Biology Harvard University, Cambridge, MA, United States 
 2015- Max Planck Institute for Coal Research, Mülheim an der Ruhr, Nordrhein-Westfalen, Germany 
Area:
fluorination chemistry for late-stage functionalization of complex natural and unnatural products and bimetallic transition metal redox catalysis
Website:
https://www.kofo.mpg.de/en/research/organic-synthesis
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106 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Bai Z, Lansbergen B, Ritter T. Addition to "Bicyclopentylation of Alcohols with Thianthrenium Reagents". Journal of the American Chemical Society. PMID 38212883 DOI: 10.1021/jacs.4c00054  0.739
2023 Miller SJ, Ritter T. Introduction: Remote and Late Stage Functionalization. Chemical Reviews. 123: 13867-13868. PMID 38148744 DOI: 10.1021/acs.chemrev.3c00800  0.348
2023 Bai Z, Lansbergen B, Ritter T. Bicyclopentylation of Alcohols with Thianthrenium Reagents. Journal of the American Chemical Society. 145: 25954-25961. PMID 38010346 DOI: 10.1021/jacs.3c10024  0.768
2023 Kim J, Müller S, Ritter T. Synthesis of α-Branched Enones via Chloroacylation of Terminal Alkenes. Angewandte Chemie (International Ed. in English). e202309498. PMID 37786992 DOI: 10.1002/anie.202309498  0.494
2022 Cheng Q, Bai Z, Tewari S, Ritter T. Bifunctional sulfilimines enable synthesis of multiple N-heterocycles from alkenes. Nature Chemistry. 14: 898-904. PMID 35871706 DOI: 10.1038/s41557-022-00997-y  0.773
2020 Cheng Q, Chen J, Lin S, Ritter T. Allylic Amination of Alkenes with Iminothianthrenes to Afford Alkyl Allylamines. Journal of the American Chemical Society. PMID 33001638 DOI: 10.1021/jacs.0c08248  0.529
2020 Berger F, Alvarez EM, Frank N, Bohdan K, Kondratiuk M, Torkowski L, Engl PS, Barletta J, Ritter T. -Substitutions at Five-Membered Hetarenes Enabled by Sulfonium Salts. Organic Letters. 22: 5671-5674. PMID 32640160 DOI: 10.1021/Acs.Orglett.0C02067  0.373
2020 Alvarez EM, Plutschack MB, Berger F, Ritter T. Site-Selective C-H Functionalization-Sulfination Sequence to Access Aryl Sulfonamides. Organic Letters. PMID 32255644 DOI: 10.1021/Acs.Orglett.0C00982  0.347
2020 Börgel J, Ritter T. Late-Stage Functionalization Chem. 6: 1877-1887. DOI: 10.1016/J.Chempr.2020.07.007  0.357
2019 Ritter T, Chen J, Li J, Plutschack M, Berger F. Regio- and Stereoselective Thianthrenation of Olefins to Access Versatile Alkenyl Electrophiles. Angewandte Chemie (International Ed. in English). PMID 31782968 DOI: 10.1002/Anie.201914215  0.374
2019 Li J, Chen J, Sang R, Ham WS, Plutschack MB, Berger F, Chabbra S, Schnegg A, Genicot C, Ritter T. Photoredox catalysis with aryl sulfonium salts enables site-selective late-stage fluorination. Nature Chemistry. PMID 31767996 DOI: 10.1038/S41557-019-0353-3  0.662
2019 Ritter T, Xu P, Zhao D, Berger F, Hamad A, Rickmeier J, Petzold R, Kondratiuk M, Bohdan K. Site-selective Late-Stage Aromatic 18F-Fluorination via Aryl Sulfonium Salts. Angewandte Chemie (International Ed. in English). PMID 31697427 DOI: 10.1002/Anie.201912567  0.347
2019 Tanwar L, Börgel J, Ritter T. Synthesis of Benzylic Alcohols by C-H Oxidation. Journal of the American Chemical Society. 141: 17983-17988. PMID 31689095 DOI: 10.1021/Jacs.9B09496  0.326
2019 Ritter T, Sang R, Korkis S, Su W, Ye F, Engl P, Berger F. Site-selective C-H Oxygenation via Aryl Sulfonium Salts. Angewandte Chemie (International Ed. in English). PMID 31475767 DOI: 10.1002/Anie.201908718  0.332
2019 Engl PS, Häring AP, Berger F, Berger G, Pérez-Bitrián A, Ritter T. C-N Cross-Couplings for Site-Selective Late-Stage Diversification via Aryl Sulfonium Salts. Journal of the American Chemical Society. PMID 31411869 DOI: 10.1021/Jacs.9B07323  0.365
2019 Ritter T, Ye F, Berger F, Jia H, Ford J, Wortman A, Borgel J, Genicot C. Aryl Sulfonium Salts for Site-selective Late-stage Trifluoromethylation. Angewandte Chemie (International Ed. in English). PMID 31389649 DOI: 10.1002/Anie.201906672  0.362
2019 Hillenbrand J, Ham WS, Ritter T. C-H Pyridonation of (Hetero-)Arenes by Pyridinium Radical Cations. Organic Letters. PMID 31240940 DOI: 10.1021/Acs.Orglett.9B02054  0.624
2019 D'Amato EM, Börgel J, Ritter T. Aromatic C-H amination in hexafluoroisopropanol. Chemical Science. 10: 2424-2428. PMID 30881670 DOI: 10.1039/C8Sc04966A  0.358
2019 Berger F, Plutschack MB, Riegger J, Yu W, Speicher S, Ho M, Frank N, Ritter T. Site-selective and versatile aromatic C-H functionalization by thianthrenation. Nature. 567: 223-228. PMID 30867606 DOI: 10.1038/S41586-019-0982-0  0.36
2019 Zhao D, Xu P, Ritter T. Palladium-Catalyzed Late-Stage Direct Arene Cyanation Chem. 5: 97-107. DOI: 10.1016/J.Chempr.2018.09.027  0.351
2018 Börgel J, Tanwar L, Berger F, Ritter T. Late-Stage Aromatic C-H Oxygenation. Journal of the American Chemical Society. PMID 30421917 DOI: 10.1021/Jacs.8B09208  0.366
2018 Ham W, Hillenbrand J, Jacq J, Genicot C, Ritter T. Divergent Late-Stage (Hetero)Aryl C-H Amination by the Pyridinium Radical Cation. Angewandte Chemie (International Ed. in English). PMID 30395385 DOI: 10.1002/Anie.201810262  0.652
2018 Pan F, Boursalian G, Ritter T. Palladium-Catalyzed Decarbonylative Difluoromethylation of Acid Chlorides at Room Temperature. Angewandte Chemie (International Ed. in English). PMID 30353979 DOI: 10.1002/Anie.201811139  0.351
2018 Sun X, Chen J, Ritter T. Catalytic dehydrogenative decarboxyolefination of carboxylic acids. Nature Chemistry. PMID 30297751 DOI: 10.1038/S41557-018-0142-4  0.343
2018 Serpier F, Pan F, Ham W, Jaqc J, Genicot C, Ritter T. Selective Methylation of Arenes via Radical C-H Functionalization Cross-Coupling Sequence. Angewandte Chemie (International Ed. in English). PMID 29893494 DOI: 10.1002/Anie.201804628  0.614
2018 Yamamoto K, Li J, Garber JAO, Rolfes JD, Boursalian GB, Borghs JC, Genicot C, Jacq J, van Gastel M, Neese F, Ritter T. Palladium-catalysed electrophilic aromatic C-H fluorination. Nature. 554: 511-514. PMID 29469096 DOI: 10.1038/Nature25749  0.623
2017 Neumann CN, Ritter T. Facile C-F Bond Formation through a Concerted Nucleophilic Aromatic Substitution Mediated by the PhenoFluor Reagent. Accounts of Chemical Research. PMID 29120599 DOI: 10.1021/Acs.Accounts.7B00413  0.417
2017 Ye F, Chen J, Ritter T. Rh-Catalyzed Anti-Markovnikov Hydrocyanation of Terminal Alkynes. Journal of the American Chemical Society. PMID 28525275 DOI: 10.1021/Jacs.7B03749  0.342
2017 Lee H, Börgel J, Ritter T. Carbon-Fluorine Reductive Elimination from Nickel(III) Complexes. Angewandte Chemie (International Ed. in English). PMID 28493645 DOI: 10.1002/Anie.201701552  0.358
2016 Campbell MG, Mercier J, Genicot C, Gouverneur V, Hooker JM, Ritter T. Bridging the gaps in (18)F PET tracer development. Nature Chemistry. 9: 1-3. PMID 27995923 DOI: 10.1038/Nchem.2693  0.537
2016 Goldberg NW, Shen X, Li J, Ritter T. AlkylFluor: Deoxyfluorination of Alcohols. Organic Letters. 18: 6102-6104. PMID 27934341 DOI: 10.1021/Acs.Orglett.6B03086  0.5
2016 Shi H, Braun A, Wang L, Liang SH, Vasdev N, Ritter T. Synthesis of (18) F-Difluoromethylarenes from Aryl (Pseudo) Halides. Angewandte Chemie (International Ed. in English). PMID 27491349 DOI: 10.1002/Anie.201604106  0.308
2016 Boursalian GB, Ham WS, Mazzotti AR, Ritter T. Charge-transfer-directed radical substitution enables para-selective C-H functionalization. Nature Chemistry. 8: 810-5. PMID 27442288 DOI: 10.1038/Nchem.2529  0.614
2016 Neumann CN, Hooker JM, Ritter T. Concerted nucleophilic aromatic substitution with (19)F(-) and (18)F(.) Nature. PMID 27281221 DOI: 10.1038/Nature17667  0.375
2016 Hoover AJ, Lazari M, Ren H, Narayanam MK, Murphy JM, van Dam RM, Hooker JM, Ritter T. A Transmetalation Reaction Enables the Synthesis of [(18)F]5-Fluorouracil from [(18)F]Fluoride for Human PET Imaging. Organometallics. 35: 1008-1014. PMID 27087736 DOI: 10.1021/Acs.Organomet.6B00059  0.312
2016 Lee H, Campbell MG, Hernández Sánchez R, Börgel J, Raynaud J, Parker SE, Ritter T. Mechanistic Insight into High-Spin Iron(I)-Catalyzed Butadiene Dimerization Organometallics. 35: 2923-2929. DOI: 10.1021/Acs.Organomet.6B00474  0.563
2016 Börgel J, Campbell MG, Ritter T. Transition Metal d-Orbital Splitting Diagrams: An Updated Educational Resource for Square Planar Transition Metal Complexes Journal of Chemical Education. 93: 118-121. DOI: 10.1021/Acs.Jchemed.5B00542  0.53
2015 D'Amato EM, Neumann CN, Ritter T. Selective Aromatic C-H Hydroxylation Enabled by η (6)-Coordination to Iridium(III). Organometallics. 34: 4626-4631. PMID 26877574 DOI: 10.1021/Acs.Organomet.5B00731  0.347
2015 McNeill E, Ritter T. 1,4-Functionalization of 1,3-dienes with low-valent iron catalysts. Accounts of Chemical Research. 48: 2330-43. PMID 26214092 DOI: 10.1021/Acs.Accounts.5B00050  0.325
2015 Shen X, Neumann CN, Kleinlein C, Goldberg NW, Ritter T. Alkyl Aryl Ether Bond Formation with PhenoFluor. Angewandte Chemie (International Ed. in English). 54: 5662-5. PMID 25800679 DOI: 10.1002/Anie.201500902  0.579
2015 Shi H, Babinski DJ, Ritter T. Modular C-H functionalization cascade of aryl iodides. Journal of the American Chemical Society. 137: 3775-8. PMID 25763682 DOI: 10.1021/Jacs.5B01082  0.746
2015 Neumann CN, Ritter T. Late-stage fluorination: fancy novelty or useful tool? Angewandte Chemie (International Ed. in English). 54: 3216-21. PMID 25653137 DOI: 10.1002/Anie.201410288  0.38
2015 Sladojevich F, McNeill E, Börgel J, Zheng SL, Ritter T. Condensed-phase, halogen-bonded CF3I and C2F5I adducts for perfluoroalkylation reactions. Angewandte Chemie (International Ed. in English). 54: 3712-6. PMID 25651531 DOI: 10.1002/Anie.201410954  0.359
2015 Fujimoto T, Ritter T. PhenoFluorMix: practical chemoselective deoxyfluorination of phenols. Organic Letters. 17: 544-7. PMID 25619627 DOI: 10.1021/Ol5035518  0.533
2015 Campbell MG, Ritter T. Modern carbon-fluorine bond forming reactions for aryl fluoride synthesis. Chemical Reviews. 115: 612-33. PMID 25474722 DOI: 10.1021/Cr500366B  0.62
2014 Campbell MG, Ritter T. Late-Stage Fluorination: From Fundamentals to Application. Organic Process Research & Development. 18: 474-480. PMID 25838756 DOI: 10.1021/Op400349G  0.539
2014 Fujimoto T, Becker F, Ritter T. PhenoFluor: Practical Synthesis, New Formulation, and Deoxyfluorination of Heteroaromatics. Organic Process Research & Development. 18: 1041-1044. PMID 25177149 DOI: 10.1021/Op500121W  0.522
2014 Campbell MG, Ritter T. Late-stage formation of carbon-fluorine bonds. Chemical Record (New York, N.Y.). 14: 482-91. PMID 24899550 DOI: 10.1002/Tcr.201402016  0.595
2014 Parker SE, Börgel J, Ritter T. 1,2-selective hydrosilylation of conjugated dienes. Journal of the American Chemical Society. 136: 4857-60. PMID 24650185 DOI: 10.1021/Ja5008596  0.341
2014 Regalado EL, Kozlowski MC, Curto JM, Ritter T, Campbell MG, Mazzotti AR, Hamper BC, Spilling CD, Mannino MP, Wan L, Yu JQ, Liu J, Welch CJ. Support of academic synthetic chemistry using separation technologies from the pharmaceutical industry. Organic & Biomolecular Chemistry. 12: 2161-6. PMID 24589831 DOI: 10.1039/C3Ob42195C  0.529
2014 Brandt JR, Lee E, Boursalian GB, Ritter T. Mechanism of Electrophilic Fluorination with Pd(IV): Fluoride Capture and Subsequent Oxidative Fluoride Transfer(.) Chemical Science (Royal Society of Chemistry : 2010). 5. PMID 24376910 DOI: 10.1039/C3Sc52367E  0.626
2014 Powers DC, Ritter T. Oxidation of Carbon-Metal Bonds Comprehensive Organic Synthesis: Second Edition. 7: 719-743. DOI: 10.1016/B978-0-08-097742-3.00727-8  0.514
2014 Liang T, Ritter T. Synthesis of Fluorides Comprehensive Organic Synthesis: Second Edition. 6: 210-238. DOI: 10.1016/B978-0-08-097742-3.00607-8  0.462
2014 Campbell MG, Hoover AJ, Ritter T. Transition metal-mediated and metal-catalyzed carbon–fluorine bond formation Topics in Organometallic Chemistry. 52. DOI: 10.1007/3418_2014_88  0.506
2014 Kornecki KP, Berry JF, Powers DC, Ritter T. Metal·Metal Bond-Containing Complexes as Catalysts for C·H Functionalization Progress in Inorganic Chemistry. 58: 225-302. DOI: 10.1002/9781118792797.ch04  0.541
2013 Mazzotti AR, Campbell MG, Tang P, Murphy JM, Ritter T. Palladium(III)-catalyzed fluorination of arylboronic acid derivatives. Journal of the American Chemical Society. 135: 14012-5. PMID 24040932 DOI: 10.1021/Ja405919Z  0.634
2013 Campbell MG, Zheng SL, Ritter T. One-dimensional palladium wires: influence of molecular changes on supramolecular structure. Inorganic Chemistry. 52: 13295-7. PMID 24032345 DOI: 10.1021/Ic4019635  0.575
2013 Boursalian GB, Ngai MY, Hojczyk KN, Ritter T. Pd-catalyzed aryl C-H imidation with arene as the limiting reagent. Journal of the American Chemical Society. 135: 13278-81. PMID 23998528 DOI: 10.1021/Ja4064926  0.698
2013 Liang T, Neumann CN, Ritter T. Introduction of fluorine and fluorine-containing functional groups. Angewandte Chemie (International Ed. in English). 52: 8214-64. PMID 23873766 DOI: 10.1002/Anie.201206566  0.577
2013 Kamlet AS, Neumann CN, Lee E, Carlin SM, Moseley CK, Stephenson N, Hooker JM, Ritter T. Application of palladium-mediated (18)F-fluorination to PET radiotracer development: overcoming hurdles to translation. Plos One. 8: e59187. PMID 23554994 DOI: 10.1371/Journal.Pone.0059187  0.608
2013 Sladojevich F, Arlow SI, Tang P, Ritter T. Late-stage deoxyfluorination of alcohols with PhenoFluor. Journal of the American Chemical Society. 135: 2470-3. PMID 23397884 DOI: 10.1021/Ja3125405  0.301
2013 Knochel P, Steib AK, Mazzotti AR, Campbell MG, Tang P, Murphy JM, Ritter T. Fluorination of Aryl Trifluoroborates Synfacts. 9: 1325-1325. DOI: 10.1055/S-0033-1340140  0.387
2013 Powers DC, Ritter T. A transition state analogue for the oxidation of binuclear palladium(II) to binuclear palladium(III) complexes Organometallics. 32: 2042-2045. DOI: 10.1021/Om4000456  0.598
2013 Liang T, Neumann CN, Ritter T. Einführung von Fluor und fluorhaltigen funktionellen Gruppen Angewandte Chemie. 125: 8372-8423. DOI: 10.1002/Ange.201206566  0.481
2012 Lee E, Hooker JM, Ritter T. Nickel-mediated oxidative fluorination for PET with aqueous [18F] fluoride. Journal of the American Chemical Society. 134: 17456-8. PMID 23061667 DOI: 10.1021/Ja3084797  0.61
2012 Powers DC, Lee E, Ariafard A, Sanford MS, Yates BF, Canty AJ, Ritter T. Connecting binuclear Pd(III) and mononuclear Pd(IV) chemistry by Pd-Pd bond cleavage. Journal of the American Chemical Society. 134: 12002-9. PMID 22804682 DOI: 10.1021/Ja304401U  0.751
2012 Powers DC, Ritter T. Bimetallic redox synergy in oxidative palladium catalysis. Accounts of Chemical Research. 45: 840-50. PMID 22029861 DOI: 10.1021/Ar2001974  0.632
2012 Raynaud J, Wu JY, Ritter T. Iron‐Catalyzed Polymerization of Isoprene and Other 1,3‐Dienes Angewandte Chemie. 51: 11805-11808. DOI: 10.1002/Ange.201205152  0.33
2011 Campbell MG, Powers DC, Raynaud J, Graham MJ, Xie P, Lee E, Ritter T. Synthesis and structure of solution-stable one-dimensional palladium wires. Nature Chemistry. 3: 949-53. PMID 22109275 DOI: 10.1038/Nchem.1197  0.744
2011 Lee E, Kamlet AS, Powers DC, Neumann CN, Boursalian GB, Furuya T, Choi DC, Hooker JM, Ritter T. A fluoride-derived electrophilic late-stage fluorination reagent for PET imaging. Science (New York, N.Y.). 334: 639-42. PMID 22053044 DOI: 10.1126/Science.1212625  0.748
2011 Huang C, Liang T, Harada S, Lee E, Ritter T. Silver-mediated trifluoromethoxylation of aryl stannanes and arylboronic acids. Journal of the American Chemical Society. 133: 13308-10. PMID 21827148 DOI: 10.1021/Ja204861A  0.694
2011 Tang P, Ritter T. Silver-mediated fluorination of aryl silanes. Tetrahedron. 67: 4449-4454. PMID 21691436 DOI: 10.1016/J.Tet.2011.02.077  0.328
2011 Furuya T, Kamlet AS, Ritter T. Catalysis for fluorination and trifluoromethylation. Nature. 473: 470-7. PMID 21614074 DOI: 10.1038/Nature10108  0.581
2011 Powers DC, Ritter T. Palladium(III) in Synthesis and Catalysis. Topics in Organometallic Chemistry. 503: 129-156. PMID 21461129 DOI: 10.1007/978-3-642-17429-2_6  0.593
2011 Chuang GJ, Wang W, Lee E, Ritter T. A dinuclear palladium catalyst for α-hydroxylation of carbonyls with O2. Journal of the American Chemical Society. 133: 1760-2. PMID 21247109 DOI: 10.1021/Ja108396K  0.653
2011 Furuya T, Ritter T. Transition metal mediated fluorination of arenes Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry. 69: 48-61. DOI: 10.5059/Yukigoseikyokaishi.69.48  0.566
2010 Furuya T, Klein JE, Ritter T. C-F Bond Formation for the Synthesis of Aryl Fluorides. Synthesis. 2010: 1804-1821. PMID 20953341 DOI: 10.1055/S-0029-1218742  0.614
2010 Powers DC, Xiao DY, Geibel MA, Ritter T. On the mechanism of palladium-catalyzed aromatic C-H oxidation. Journal of the American Chemical Society. 132: 14530-6. PMID 20873835 DOI: 10.1021/Ja1054274  0.614
2010 Powers DC, Benitez D, Tkatchouk E, Goddard WA, Ritter T. Bimetallic reductive elimination from dinuclear Pd(III) complexes. Journal of the American Chemical Society. 132: 14092-103. PMID 20858006 DOI: 10.1021/Ja1036644  0.72
2010 Tang P, Furuya T, Ritter T. Silver-catalyzed late-stage fluorination. Journal of the American Chemical Society. 132: 12150-4. PMID 20695434 DOI: 10.1021/Ja105834T  0.611
2010 Furuya T, Benitez D, Tkatchouk E, Strom AE, Tang P, Goddard WA, Ritter T. Mechanism of C-F reductive elimination from palladium(IV) fluorides. Journal of the American Chemical Society. 132: 3793-807. PMID 20196595 DOI: 10.1021/Ja909371T  0.706
2009 Powers DC, Ritter T. Bimetallic Pd(III) complexes in palladium-catalysed carbon–heteroatom bond formation. Nature Chemistry. 1: 302-9. PMID 21500602 DOI: 10.1038/Nchem.246  0.62
2009 Powers DC, Geibel MA, Klein JE, Ritter T. Bimetallic palladium catalysis: direct observation of Pd(III)-Pd(III) intermediates. Journal of the American Chemical Society. 131: 17050-1. PMID 19899740 DOI: 10.1021/Ja906935C  0.589
2009 Wu JY, Moreau B, Ritter T. Iron-catalyzed 1,4-hydroboration of 1,3-dienes. Journal of the American Chemical Society. 131: 12915-7. PMID 19702262 DOI: 10.1021/Ja9048493  0.304
2009 Furuya T, Ritter T. Fluorination of boronic acids mediated by silver(I) triflate. Organic Letters. 11: 2860-3. PMID 19507870 DOI: 10.1021/Ol901113T  0.586
2009 Furuya T, Strom AE, Ritter T. Silver-mediated fluorination of functionalized aryl stannanes. Journal of the American Chemical Society. 131: 1662-3. PMID 19191693 DOI: 10.1021/Ja8086664  0.631
2009 Furuya T, Strom AE, Ritter T. Fluorination of Aryl Stannanes Mediated by AgOTf Synfacts. 2009: 543-543. DOI: 10.1055/S-0028-1088040  0.59
2009 Powers DC, Ritter T. Erratum: Bimetallic Pd(III) complexes in palladium-catalysed carbon–heteroatom bond formation Nature Chemistry. 1: 419-419. DOI: 10.1038/Nchem.294  0.58
2008 Furuya T, Kuttruff CA, Ritter T. Carbon-fluorine bond formation. Current Opinion in Drug Discovery & Development. 11: 803-19. PMID 18946845  0.57
2008 Furuya T, Ritter T. Carbon-fluorine reductive elimination from a high-valent palladium fluoride. Journal of the American Chemical Society. 130: 10060-1. PMID 18616246 DOI: 10.1021/Ja803187X  0.57
2008 Furuya T, Kaiser HM, Ritter T. Palladium-mediated fluorination of arylboronic acids. Angewandte Chemie (International Ed. in English). 47: 5993-6. PMID 18604865 DOI: 10.1002/Anie.200802164  0.536
2008 Furuya T, Kaiser HM, Ritter T. Pd-Mediated Fluorination of Arylboronic Acids Synfacts. 2008: 1087-1087. DOI: 10.1055/S-2008-1078231  0.551
2008 Furuya T, Ritter T. Carbon-fluorine reductive elimination from a high-valent palladium fluoride [Journal of the American Chemical Society (2008) 130, (10060-10061)) Journal of the American Chemical Society. 130: 12834. DOI: 10.1021/ja8065013  0.48
2008 Furuya T, Kaiser H, Ritter T. Palladiumvermittelte Fluorierung von Arylboronsäuren Angewandte Chemie. 120: 6082-6085. DOI: 10.1002/Ange.200802164  0.459
2007 Berlin JM, Campbell K, Ritter T, Funk TW, Chlenov A, Grubbs RH. Ruthenium-catalyzed ring-closing metathesis to form tetrasubstituted olefins. Organic Letters. 9: 1339-42. PMID 17343392 DOI: 10.1055/S-2007-968539  0.774
2007 Blum AP, Ritter T, Grubbs RH. Synthesis of N-heterocylic carbene-containing metal complexes from 2-(pentafluorophenyl)imidazolidines Organometallics. 26: 2122-2124. DOI: 10.1021/Om060949F  0.479
2006 Ritter T, Day MW, Grubbs RH. Rate acceleration in olefin metathesis through a fluorine-ruthenium interaction. Journal of the American Chemical Society. 128: 11768-9. PMID 16953611 DOI: 10.1021/Ja064091X  0.409
2006 Waltman AW, Ritter T, Grubbs RH. Rearrangement of N-heterocylic carbenes involving heterocycle cleavage Organometallics. 25: 4238-4239. DOI: 10.1021/Om060528Y  0.77
2006 Ritter T, Hejl A, Wenzel AG, Funk TW, Grubbs RH. A standard system of characterization for olefin metathesis catalysts Organometallics. 25: 5740-5745. DOI: 10.1021/Om060520O  0.739
2005 Ritter T, Kvaernø L, Werder M, Hauser H, Carreira EM. Heterocyclic ring scaffolds as small-molecule cholesterol absorption inhibitors. Organic & Biomolecular Chemistry. 3: 3514-23. PMID 16172689 DOI: 10.1039/B510100J  0.381
2005 Ritter T, Carreira EM. 1,2,4-oxadiazolidinones as configurationally stable chiral building blocks. Angewandte Chemie (International Ed. in English). 44: 936-8. PMID 15624222 DOI: 10.1002/Anie.200461934  0.38
2004 Ritter T, Zarotti P, Carreira EM. Diastereoselective phenol para-alkylation: access to a cross-conjugated cyclohexadienone en route to resiniferatoxin. Organic Letters. 6: 4371-4. PMID 15524486 DOI: 10.1021/Ol0480832  0.48
2004 Kvaernø L, Ritter T, Werder M, Hauser H, Carreira EM. An in vitro assay for evaluation of small-molecule inhibitors of cholesterol absorption. Angewandte Chemie (International Ed. in English). 43: 4653-6. PMID 15352196 DOI: 10.1002/Anie.200460348  0.35
2004 Ritter T, Stanek K, Larrosa I, Carreira EM. Mild cleavage of aryl mesylates: methanesulfonate as potent protecting group for phenols. Organic Letters. 6: 1513-4. PMID 15101780 DOI: 10.1021/Ol049514J  0.468
2002 Ritter T, Carreira EM. The diazonamides: the plot thickens. Angewandte Chemie (International Ed. in English). 41: 2489-95. PMID 12203512 DOI: 10.1002/1521-3773(20020715)41:14<2489::Aid-Anie2489>3.0.Co;2-V  0.35
2002 Ritter T, Carreira EM. Die Diazonamide: immer für Überraschungen gut Angewandte Chemie. 114: 2601-2606. DOI: 10.1002/1521-3757(20020715)114:14<2601::Aid-Ange2601>3.0.Co;2-B  0.336
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