Year |
Citation |
Score |
2024 |
Kozhummal H, Das SK, Cooze C, Lundgren RJ. Enantio- and Z-Selective δ-Hydroarylation of Aryl-Substituted 1,3-Dienes via Rh-Catalyzed Conjugate Addition. Angewandte Chemie (International Ed. in English). e202406102. PMID 38753742 DOI: 10.1002/anie.202406102 |
0.382 |
|
2023 |
Qiqige Q, Lundgren RJ, Kong D. Combining Enantioselective Rh-Catalyzed Conjugate Addition and Ir-Catalyzed Allylic Alkylation in Stereodivergent, Multicomponent Coupling Reactions to Form Three Stereocenters. Chemistry (Weinheim An Der Bergstrasse, Germany). e202300727. PMID 36898971 DOI: 10.1002/chem.202300727 |
0.37 |
|
2021 |
Doyle MGJ, Gabbey AL, McNutt W, Lundgren RJ. Enantioselective Tertiary Electrophile (Hetero)Benzylation: Pd-Catalyzed Substitution of Isoprene Monoxide with Arylacetates*. Angewandte Chemie (International Ed. in English). 60: 26495-26499. PMID 34658132 DOI: 10.1002/anie.202110525 |
0.36 |
|
2021 |
Cooze CJC, McNutt W, Schoetz MD, Sosunovych B, Grigoryan S, Lundgren RJ. Diastereo-, Enantio-, and -Selective α,δ-Difunctionalization of Electron-Deficient Dienes Initiated by Rh-Catalyzed Conjugate Addition. Journal of the American Chemical Society. PMID 34253021 DOI: 10.1021/jacs.1c05427 |
0.441 |
|
2021 |
Cooze CJC, McNutt W, Schoetz MD, Sosunovych B, Grigoryan S, Lundgren RJ. Diastereo-, Enantio-, and -Selective α,δ-Difunctionalization of Electron-Deficient Dienes Initiated by Rh-Catalyzed Conjugate Addition. Journal of the American Chemical Society. PMID 34253021 DOI: 10.1021/jacs.1c05427 |
0.441 |
|
2021 |
Doyle MGJ, Lundgren RJ. Oxidative cross-coupling processes inspired by the Chan-Lam reaction. Chemical Communications (Cambridge, England). PMID 33623942 DOI: 10.1039/d1cc00213a |
0.429 |
|
2020 |
Kong D, Moon PJ, Lui EKJ, Bsharat O, Lundgren RJ. Direct reversible decarboxylation from stable organic acids in dimethylformamide solution. Science (New York, N.Y.). PMID 32554626 DOI: 10.1126/Science.Abb4129 |
0.351 |
|
2020 |
Moon PJ, Lundgren RJ. Metal-Catalyzed Ionic Decarboxylative Cross-Coupling Reactions of C(sp3) Acids: Reaction Development, Mechanisms, and Application Acs Catalysis. 10: 1742-1753. DOI: 10.1021/Acscatal.9B04956 |
0.476 |
|
2019 |
Kong D, Moon P, Bsharat O, Lundgren RJ. Direct Catalytic Decarboxylative Amination of Aryl Acetic Acids. Angewandte Chemie (International Ed. in English). PMID 31721408 DOI: 10.1002/Anie.201912518 |
0.406 |
|
2019 |
Cooze C, Dada R, Lundgren RJ. Formic Acid Mediated Direct Z-Selective Reductive Coupling of Dienes and Aldehydes. Angewandte Chemie (International Ed. in English). PMID 31215135 DOI: 10.1002/Anie.201905540 |
0.492 |
|
2018 |
Moon PJ, Wei Z, Lundgren RJ. Direct Catalytic Enantioselective Benzylation from Aryl Acetic Acids. Journal of the American Chemical Society. PMID 30449096 DOI: 10.1021/Jacs.8B11390 |
0.468 |
|
2018 |
Kong D, Moon PJ, Qian W, Lundgren RJ. Expanding the limit of Pd-catalyzed decarboxylative benzylations. Chemical Communications (Cambridge, England). PMID 29696284 DOI: 10.1039/C8Cc02380H |
0.478 |
|
2018 |
Thomas BN, Moon PJ, Yin S, Brown A, Lundgren RJ. -Selective iridium-catalyzed cross-coupling of allylic carbonates and α-diazo esters. Chemical Science. 9: 238-244. PMID 29629093 DOI: 10.1039/C7Sc04283C |
0.517 |
|
2018 |
Moon PJ, Fahandej-Sadi A, Qian W, Lundgren RJ. Decarboxylative Benzylation of sp2-Organoboron Reagents. Angewandte Chemie (International Ed. in English). PMID 29512252 DOI: 10.1002/Anie.201800829 |
0.496 |
|
2018 |
Dada R, Wei Z, Gui R, Lundgren RJ. Chemoselective Z-Olefin Synthesis via Rh-Catalyzed, Formate Mediated 1,6-Reduction. Angewandte Chemie (International Ed. in English). PMID 29441704 DOI: 10.1002/Anie.201800361 |
0.428 |
|
2017 |
Lundgren RJ. Catalytic, Reversible Arylation of Phosphines and Sulfides. Angewandte Chemie (International Ed. in English). PMID 28752559 DOI: 10.1002/Anie.201706328 |
0.484 |
|
2017 |
Moon PJ, Lundgren RJ. Copper-Mediated Oxidative α-Arylation of Carbonyl Compounds with Boronic Acid Derivatives Synlett. 28: 515-520. DOI: 10.1055/S-0036-1589841 |
0.449 |
|
2017 |
Fahandej-Sadi A, Lundgren RJ. Copper-Mediated Synthesis of Monofluoro Aryl Acetates via Decarboxylative Cross-Coupling Synlett. 28: 2886-2890. DOI: 10.1055/S-0036-1588516 |
0.481 |
|
2016 |
Moon PJ, Yin S, Lundgren RJ. Ambient Decarboxylative Arylation of Malonate Half-Esters via Oxidative Catalysis. Journal of the American Chemical Society. PMID 27736064 DOI: 10.1021/Jacs.6B08906 |
0.43 |
|
2016 |
Moon PJ, Halperin HM, Lundgren RJ. Oxidative Coupling of Aryl Boron Reagents with sp(3) -Carbon Nucleophiles: The Enolate Chan-Evans-Lam Reaction. Angewandte Chemie (International Ed. in English). PMID 26732351 DOI: 10.1002/Anie.201510558 |
0.488 |
|
2015 |
Lundgren RJ, Thomas BN. Chemo- and regioselective reductive transposition of allylic alcohol derivatives via iridium or rhodium catalysis. Chemical Communications (Cambridge, England). PMID 26587569 DOI: 10.1039/C5Cc07993D |
0.425 |
|
2013 |
Cordier CJ, Lundgren RJ, Fu GC. Enantioconvergent cross-couplings of racemic alkylmetal reagents with unactivated secondary alkyl electrophiles: catalytic asymmetric Negishi α-alkylations of N-Boc-pyrrolidine. Journal of the American Chemical Society. 135: 10946-9. PMID 23869442 DOI: 10.1021/Ja4054114 |
0.731 |
|
2013 |
Bissember AC, Lundgren RJ, Creutz SE, Peters JC, Fu GC. Transition-metal-catalyzed alkylations of amines with alkyl halides: photoinduced, copper-catalyzed couplings of carbazoles. Angewandte Chemie (International Ed. in English). 52: 5129-33. PMID 23564657 DOI: 10.1002/Anie.201301202 |
0.734 |
|
2013 |
Lundgren RJ, Wilsily A, Marion N, Ma C, Chung YK, Fu GC. Catalytic asymmetric C-N bond formation: phosphine-catalyzed intra- and intermolecular γ-addition of nitrogen nucleophiles to allenoates and alkynoates. Angewandte Chemie (International Ed. in English). 52: 2525-8. PMID 23339132 DOI: 10.1002/Anie.201208957 |
0.756 |
|
2013 |
Alsabeh PG, Lundgren RJ, McDonald R, Johansson Seechurn CC, Colacot TJ, Stradiotto M. An examination of the palladium/Mor-DalPhos catalyst system in the context of selective ammonia monoarylation at room temperature. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 2131-41. PMID 23293095 DOI: 10.1002/Chem.201203640 |
0.623 |
|
2012 |
Lundgren RJ, Stradiotto M. Addressing challenges in palladium-catalyzed cross-coupling reactions through ligand design. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 9758-69. PMID 22786694 DOI: 10.1002/Chem.201201195 |
0.649 |
|
2012 |
Lundgren RJ, Stradiotto M. Recent advances in the buchwald-hartwig amination reaction enabled by the application of sterically demanding phosphine ancillary ligands Aldrichimica Acta. 45: 59-62. |
0.567 |
|
2011 |
Alsabeh PG, Lundgren RJ, Longobardi LE, Stradiotto M. Palladium-catalyzed synthesis of indoles via ammonia cross-coupling-alkyne cyclization. Chemical Communications (Cambridge, England). 47: 6936-8. PMID 21594239 DOI: 10.1039/C1Cc11874A |
0.734 |
|
2011 |
Hesp KD, Lundgren RJ, Stradiotto M. Palladium-catalyzed mono-α-arylation of acetone with aryl halides and tosylates. Journal of the American Chemical Society. 133: 5194-7. PMID 21417401 DOI: 10.1021/Ja200009C |
0.722 |
|
2011 |
Alsabeh PG, Lundgren RJ, Longobardi LE, Stradiotto M. Pd-Catalyzed Synthesis of Indoles via NH3 Cross-Coupling-AlkyneCyclization Synfacts. 2011: 832-832. DOI: 10.1055/S-0030-1260858 |
0.579 |
|
2011 |
Lundgren RJ, Hesp KD, Stradiotto M. Design of new "dalPhos" P,N-ligands: Applications in transition-metal catalysis Synlett. 2443-2458. DOI: 10.1055/S-0030-1260321 |
0.574 |
|
2011 |
Stradiotto M, Lundgren R. Palladium-Catalyzed Cross-Coupling with Hydrazine Synfacts. 2011: 0204-0204. DOI: 10.1055/S-0030-1259236 |
0.586 |
|
2010 |
Lundgren RJ, Stradiotto M. Palladium-catalyzed cross-coupling of aryl chlorides and tosylates with hydrazine. Angewandte Chemie (International Ed. in English). 49: 8686-90. PMID 20931641 DOI: 10.1002/Anie.201003764 |
0.712 |
|
2010 |
Lundgren RJ, Stradiotto M. Transition-metal-catalyzed trifluoromethylation of aryl halides. Angewandte Chemie (International Ed. in English). 49: 9322-4. PMID 20878960 DOI: 10.1002/Anie.201004051 |
0.657 |
|
2010 |
Lundgren RJ, Peters BD, Alsabeh PG, Stradiotto M. A P,N-ligand for palladium-catalyzed ammonia arylation: coupling of deactivated aryl chlorides, chemoselective arylations, and room temperature reactions. Angewandte Chemie (International Ed. in English). 49: 4071-4. PMID 20437437 DOI: 10.1002/Anie.201000526 |
0.743 |
|
2010 |
Lundgren RJ, Sappong-Kumankumah A, Stradiotto M. A highly versatile catalyst system for the cross-coupling of aryl chlorides and amines. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 1983-91. PMID 20024992 DOI: 10.1002/Chem.200902316 |
0.718 |
|
2010 |
Stradiotto M, Hesp KD, Lundgren RJ. Zwitterionic relatives of cationic platinum group metal complexes: applications in stoichiometric and catalytic sigma-bond activation. Angewandte Chemie (International Ed. in English). 49: 494-512. PMID 19998395 DOI: 10.1002/Anie.200904093 |
0.653 |
|
2010 |
Lundgren RJ, Peters BD, Alsabeh PG, Stradiotto M. A P,N-Ligand for the Palladium-Catalyzed Arylation of Ammonia Synfacts. 2010: 940-940. DOI: 10.1055/S-0030-1257754 |
0.608 |
|
2010 |
Lundgren RJ, Sappong-Kumankumah A, Stradiotto M. A General Catalyst System for Amination of Aryl Chlorides Synfacts. 2010: 580-580. DOI: 10.1055/S-0029-1219677 |
0.546 |
|
2010 |
Lundgren RJ, Stradiotto M. Übergangsmetallkatalysierte Trifluormethylierung von Arylhalogeniden Angewandte Chemie. 122: 9510-9512. DOI: 10.1002/Ange.201004051 |
0.45 |
|
2010 |
Stradiotto M, Hesp KD, Lundgren RJ. Zwitterionische Verwandte kationischer Platinmetallkomplexe: Anwendungen in der stöchiometrischen und katalytischen σ‐Bindungsaktivierung Angewandte Chemie. 122: 504-523. DOI: 10.1002/Ange.200904093 |
0.477 |
|
2008 |
Lundgren RJ, Stradiotto M. Rapid ketone transfer hydrogenation by employing simple, in situ prepared iridium(I) precatalysts supported by "non-N--H" P,N ligands. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 10388-95. PMID 18924188 DOI: 10.1002/Chem.200801530 |
0.697 |
|
2008 |
Lundgren RJ, Rankin MA, McDonald R, Stradiotto M. Neutral, cationic, and zwitterionic ruthenium(II) atom transfer radical addition catalysts supported by P,N-substituted indene or indenide ligands Organometallics. 27: 254-258. DOI: 10.1021/Om700914K |
0.615 |
|
2007 |
Lundgren RJ, Rankin MA, McDonald R, Schatte G, Stradiotto M. A formally zwitterionic ruthenium catalyst precursor for the transfer hydrogenation of ketones that does not feature an ancillary ligand N-H functionality. Angewandte Chemie (International Ed. in English). 46: 4732-5. PMID 17508385 DOI: 10.1002/Anie.200700345 |
0.679 |
|
2007 |
MacInnis MC, Maclean DF, Lundgren RJ, Mcdonald R, Turculet L. Synthesis and reactivity of platinum group metal complexes featuring the new pincer-like bis(phosphino)silyl ligand [K3-(2-Ph 2PC6H4)2SiMe]- ([PSiP]): Application in the ruthenium-mediated transfer hydrogenation of Ketones Organometallics. 26: 6522-6525. DOI: 10.1021/Om7009528 |
0.44 |
|
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