Year |
Citation |
Score |
2023 |
Ibsen GM, Menezes da Silva VH, Pettigrew JC, Neufeldt SR. Triflate-Selective Suzuki Cross-Coupling of Chloro- and Bromoaryl Triflates Under Ligand-Free Conditions. Chemistry, An Asian Journal. e202300036. PMID 36965027 DOI: 10.1002/asia.202300036 |
0.325 |
|
2022 |
Norman JP, Larson NG, Neufeldt SR. Different Oxidative Addition Mechanisms for 12- and 14-Electron Palladium(0) Explain Ligand-Controlled Divergent Site Selectivity. Acs Catalysis. 12: 8822-8828. PMID 37601556 DOI: 10.1021/acscatal.2c01698 |
0.347 |
|
2022 |
Norman JP, Larson NG, Entz ED, Neufeldt SR. Unconventional Site Selectivity in Palladium-Catalyzed Cross-Couplings of Dichloroheteroarenes under Ligand-Controlled and Ligand-Free Systems. The Journal of Organic Chemistry. 87: 7414-7421. PMID 35584051 DOI: 10.1021/acs.joc.2c00665 |
0.422 |
|
2021 |
Elias EK, Rehbein SM, Neufeldt SR. Solvent coordination to palladium can invert the selectivity of oxidative addition. Chemical Science. 13: 1618-1628. PMID 35282616 DOI: 10.1039/d1sc05862b |
0.319 |
|
2021 |
Humke JN, Daley RA, Morrenzin AS, Neufeldt SR, Topczewski JJ. Combined Experimental and Computational Mechanistic Investigation of the Palladium-Catalyzed Decarboxylative Cross-Coupling of Sodium Benzoates with Chloroarenes. The Journal of Organic Chemistry. PMID 34339213 DOI: 10.1021/acs.joc.1c00910 |
0.35 |
|
2020 |
Entz ED, Russell JEA, Hooker LV, Neufeldt SR. Small Phosphine Ligands Enable Selective Oxidative Addition of Ar-O over Ar-Cl Bonds at Nickel(0). Journal of the American Chemical Society. 142: 15454-15463. PMID 32805116 DOI: 10.1021/jacs.0c06995 |
0.361 |
|
2019 |
Russell JEA, Entz ED, Joyce IM, Neufeldt SR. Nickel-Catalyzed Stille Cross Coupling of C-O Electrophiles. Acs Catalysis. 9: 3304-3310. PMID 31057986 DOI: 10.1021/acscatal.9b00744 |
0.323 |
|
2015 |
Neufeldt SR, Jiménez-Osés G, Huckins JR, Thiel OR, Houk KN. Pyridine N-Oxide vs Pyridine Substrates for Rh(III)-Catalyzed Oxidative C-H Bond Functionalization. Journal of the American Chemical Society. 137: 9843-54. PMID 26197041 DOI: 10.1021/Jacs.5B03535 |
0.713 |
|
2014 |
Neufeldt SR, Jiménez-Osés G, Comins DL, Houk KN. A twist on facial selectivity of hydride reductions of cyclic ketones: twist-boat conformers in cyclohexanone, piperidone, and tropinone reactions. The Journal of Organic Chemistry. 79: 11609-18. PMID 25372509 DOI: 10.1021/Jo5022635 |
0.557 |
|
2013 |
Seigerman CK, Micyus TM, Neufeldt SR, Sanford MS. Palladium-Catalyzed C-H Arylation Using Aryltrifluoroborates in Conjunction with a Mn(III) Oxidant under Mild Conditions. Tetrahedron. 69: 5580-5587. PMID 23888087 DOI: 10.1016/J.Tet.2013.04.114 |
0.715 |
|
2013 |
Neufeldt SR, Seigerman CK, Sanford MS. Mild palladium-catalyzed C-H alkylation using potassium alkyltrifluoroborates in combination with MnF3 Organic Letters. 15: 2302-2305. PMID 23597105 DOI: 10.1021/Ol400888R |
0.717 |
|
2013 |
Neufeldt SR, Sanford MS. Asymmetric chiral ligand-directed alkene dioxygenation Organic Letters. 15: 46-49. PMID 23249401 DOI: 10.1021/Ol303003G |
0.586 |
|
2013 |
Seigerman CK, Micyus TM, Neufeldt SR, Sanford MS. Palladium-catalyzed C-H arylation using aryltrifluoroborates in conjunction with a MnIII oxidant under mild conditions Tetrahedron. 69: 5580-5587. DOI: 10.1016/j.tet.2013.04.114 |
0.665 |
|
2012 |
Neufeldt SR, Sanford MS. Combining Transition Metal Catalysis with Radical Chemistry: Dramatic Acceleration of Palladium-Catalyzed C-H Arylation with Diaryliodonium Salts. Advanced Synthesis & Catalysis. 354: 3517-3522. PMID 23950736 DOI: 10.1002/Adsc.201200738 |
0.642 |
|
2012 |
Neufeldt SR, Sanford MS. Controlling site selectivity in palladium-catalyzed C-H bond functionalization Accounts of Chemical Research. 45: 936-946. PMID 22554114 DOI: 10.1021/Ar300014F |
0.687 |
|
2012 |
Kalyani D, McMurtrey KB, Neufeldt SR, Sanford MS. ChemInform Abstract: Room-Temperature C-H Arylation: Merger of Pd-Catalyzed C-H Functionalization and Visible-Light Photocatalysis. Cheminform. 43: no-no. DOI: 10.1002/chin.201219090 |
0.705 |
|
2012 |
Neufeldt SR, Sanford MS. Combining transition metal catalysis with radical chemistry: Dramatic acceleration of palladium-catalyzed C-H arylation with diaryliodonium salts Advanced Synthesis and Catalysis. 354: 3517-3522. DOI: 10.1002/adsc.201200738 |
0.626 |
|
2011 |
Kalyani D, McMurtrey KB, Neufeldt SR, Sanford MS. Room-temperature C-H arylation: merger of Pd-catalyzed C-H functionalization and visible-light photocatalysis. Journal of the American Chemical Society. 133: 18566-9. PMID 22047138 DOI: 10.1021/Ja208068W |
0.717 |
|
2010 |
Neufeldt SR, Sanford MS. O-acetyl oximes as transformable directing groups for Pd-catalyzed C-H bond functionalization Organic Letters. 12: 532-535. PMID 20041702 DOI: 10.1021/Ol902720D |
0.669 |
|
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