Year |
Citation |
Score |
2023 |
Miller SJ, Ritter T. Introduction: Remote and Late Stage Functionalization. Chemical Reviews. 123: 13867-13868. PMID 38148744 DOI: 10.1021/acs.chemrev.3c00800 |
0.347 |
|
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 |
0.491 |
|
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 |
0.507 |
|
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 |
0.525 |
|
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 |
0.351 |
|
2020 |
Börgel J, Ritter T. Late-Stage Functionalization Chem. 6: 1877-1887. DOI: 10.1016/J.Chempr.2020.07.007 |
0.356 |
|
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 |
0.379 |
|
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 |
0.665 |
|
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 |
0.358 |
|
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 |
0.341 |
|
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 |
0.362 |
|
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 |
0.363 |
|
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 |
0.622 |
|
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 |
0.361 |
|
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 |
0.364 |
|
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 |
0.373 |
|
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 |
0.651 |
|
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 |
0.35 |
|
2018 |
Sun X, Chen J, Ritter T. Catalytic dehydrogenative decarboxyolefination of carboxylic acids. Nature Chemistry. PMID 30297751 DOI: 10.1038/S41557-018-0142-4 |
0.346 |
|
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 |
0.625 |
|
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 |
0.422 |
|
2017 |
Beyzavi MH, Mandal D, Strebl MG, Neumann CN, D'Amato EM, Chen J, Hooker JM, Ritter T. (18)F-Deoxyfluorination of Phenols via Ru π-Complexes. Acs Central Science. 3: 944-948. PMID 28979935 DOI: 10.1021/Acscentsci.7B00195 |
0.31 |
|
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 |
0.339 |
|
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 |
0.376 |
|
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 |
0.541 |
|
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 |
0.469 |
|
2016 |
Neumann CN, Ritter T. C-H fluorination: U can fluorinate unactivated bonds. Nature Chemistry. 8: 822-3. PMID 27554406 DOI: 10.1038/Nchem.2604 |
0.305 |
|
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 |
0.314 |
|
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 |
0.382 |
|
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 |
0.319 |
|
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 |
0.567 |
|
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 |
0.533 |
|
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 |
0.357 |
|
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 |
0.331 |
|
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 |
0.571 |
|
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 |
0.745 |
|
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 |
0.381 |
|
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 |
0.527 |
|
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 |
0.622 |
|
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 |
0.52 |
|
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 |
0.599 |
|
2014 |
Ren H, Wey HY, Strebl M, Neelamegam R, Ritter T, Hooker JM. Synthesis and imaging validation of [¹⁸F]MDL100907 enabled by Ni-mediated fluorination. Acs Chemical Neuroscience. 5: 611-5. PMID 24845956 DOI: 10.1021/Cn500078E |
0.3 |
|
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 |
0.349 |
|
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 |
0.635 |
|
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 |
0.522 |
|
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 |
0.46 |
|
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 |
0.513 |
|
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 |
0.547 |
|
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 |
0.638 |
|
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 |
0.581 |
|
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 |
0.702 |
|
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 |
0.58 |
|
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 |
0.611 |
|
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 |
0.391 |
|
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 |
0.607 |
|
2013 |
Liang T, Neumann CN, Ritter T. Einführung von Fluor und fluorhaltigen funktionellen Gruppen Angewandte Chemie. 125: 8372-8423. DOI: 10.1002/Ange.201206566 |
0.486 |
|
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 |
0.616 |
|
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 |
0.754 |
|
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 |
0.643 |
|
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 |
0.336 |
|
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 |
0.746 |
|
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 |
0.697 |
|
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 |
0.329 |
|
2011 |
Furuya T, Kamlet AS, Ritter T. Catalysis for fluorination and trifluoromethylation. Nature. 473: 470-7. PMID 21614074 DOI: 10.1038/Nature10108 |
0.583 |
|
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 |
0.602 |
|
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 |
0.66 |
|
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 |
0.571 |
|
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 |
0.62 |
|
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 |
0.624 |
|
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 |
0.726 |
|
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 |
0.615 |
|
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 |
0.714 |
|
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 |
0.631 |
|
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 |
0.599 |
|
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 |
0.632 |
|
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 |
0.589 |
|
2008 |
Furuya T, Kuttruff CA, Ritter T. Carbon-fluorine bond formation. Current Opinion in Drug Discovery & Development. 11: 803-19. PMID 18946845 |
0.574 |
|
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 |
0.576 |
|
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 |
0.539 |
|
2008 |
Furuya T, Kaiser HM, Ritter T. Pd-Mediated Fluorination of Arylboronic Acids Synfacts. 2008: 1087-1087. DOI: 10.1055/S-2008-1078231 |
0.56 |
|
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 |
0.483 |
|
2008 |
Furuya T, Kaiser H, Ritter T. Palladiumvermittelte Fluorierung von Arylboronsäuren Angewandte Chemie. 120: 6082-6085. DOI: 10.1002/Ange.200802164 |
0.46 |
|
2008 |
Ritter T, Carreira EM, Plenio H, Datta A, Siemsen P, Felber B, Gutiérrez BE, Dixneuf PH, Bruneau C. C-H Transformation at Terminal Alkynes Handbook of C-H Transformations: Applications in Organic Synthesis. 1: 29-85. DOI: 10.1002/9783527619450.ch3 |
0.304 |
|
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 |
0.769 |
|
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 |
0.48 |
|
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 |
0.411 |
|
2006 |
Waltman AW, Ritter T, Grubbs RH. Rearrangement of N-heterocylic carbenes involving heterocycle cleavage Organometallics. 25: 4238-4239. DOI: 10.1021/Om060528Y |
0.763 |
|
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 |
0.732 |
|
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 |
0.383 |
|
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 |
0.377 |
|
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 |
0.475 |
|
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 |
0.351 |
|
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 |
0.464 |
|
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 |
0.349 |
|
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 |
0.337 |
|
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