Year |
Citation |
Score |
2024 |
Lin PC, Wong CD, Jarvo ER. Cross-selective Deoxygenative Coupling of Aliphatic Alcohols: Installation of Methyl Groups including Isotopic Labels by Nickel Catalysis. Angewandte Chemie (International Ed. in English). e202403119. PMID 38604974 DOI: 10.1002/anie.202403119 |
0.481 |
|
2023 |
Herbert CA, Jarvo ER. Nickel-Catalyzed Stereoselective Coupling Reactions of Benzylic and Alkyl Alcohol Derivatives. Accounts of Chemical Research. PMID 37936256 DOI: 10.1021/acs.accounts.3c00547 |
0.601 |
|
2023 |
Chen PP, McGinnis TM, Lin PC, Hong X, Jarvo ER. A Nickel-Catalyzed Cross-Electrophile Coupling Reaction of 1,3-Dimesylates for Alkylcyclopropane Synthesis: Investigation of Stereochemical Outcomes and Radical Lifetimes. Acs Catalysis. 13: 5472-5481. PMID 37123596 DOI: 10.1021/acscatal.3c00905 |
0.472 |
|
2023 |
Lin PC, Joshi C, McGinnis TM, Mallojjala SC, Sanford AB, Hirschi JS, Jarvo ER. Stereospecific Nickel-Catalyzed Cross-Electrophile Coupling Reaction of Alkyl Mesylates and Allylic Difluorides to Access Enantioenriched Vinyl Fluoride-Substituted Cyclopropanes. Acs Catalysis. 13: 4488-4499. PMID 37066042 DOI: 10.1021/acscatal.3c00257 |
0.507 |
|
2022 |
Hirbawi N, Lin PC, Jarvo ER. Halogenation Reactions of Alkyl Alcohols Employing Methyl Grignard Reagents. The Journal of Organic Chemistry. 87: 12352-12369. PMID 36049783 DOI: 10.1021/acs.joc.2c01590 |
0.479 |
|
2022 |
Hewitt KA, Herbert CA, Jarvo ER. Synthesis of Vicinal Carbocycles by Intramolecular Nickel-Catalyzed Conjunctive Cross-Electrophile Coupling Reaction. Organic Letters. 24: 6093-6098. PMID 35926218 DOI: 10.1021/acs.orglett.2c02481 |
0.565 |
|
2022 |
McGinnis TM, Thane TA, Jarvo ER. Zinc-Mediated Transformation of 1,3-Diols to Cyclopropanes for Late-Stage Modification of Natural Products and Medicinal Agents. Organic Letters. 24: 5619-5623. PMID 35867876 DOI: 10.1021/acs.orglett.2c02362 |
0.39 |
|
2022 |
Thane TA, Jarvo ER. Ligand-Based Control of Nickel Catalysts: Switching Chemoselectivity from One-Electron to Two-Electron Pathways in Competing Reactions of 4-Halotetrahydropyrans. Organic Letters. PMID 35559652 DOI: 10.1021/acs.orglett.2c01335 |
0.33 |
|
2021 |
Hewitt KA, Herbert CA, Matus AC, Jarvo ER. Nickel-Catalyzed Kumada Cross-Coupling Reactions of Benzylic Sulfonamides. Molecules (Basel, Switzerland). 26. PMID 34641491 DOI: 10.3390/molecules26195947 |
0.553 |
|
2021 |
Sanford AB, Jarvo ER. Harnessing C-O Bonds in Stereoselective Cross-Coupling and Cross-Electrophile Coupling Reactions. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 32: 1151-1156. PMID 34354327 DOI: 10.1055/s-0040-1705987 |
0.462 |
|
2020 |
Sanford AB, Tollefson EJ, Jarvo ER. Stereospecific Cross-Coupling Reactions Provide Conformationally-Biased Arylalkanes with Anti-Leukemia Activity. Israel Journal of Chemistry. 60: 402-405. PMID 33442068 DOI: 10.1002/ijch.201900071 |
0.827 |
|
2020 |
Sanford AB, Thane TA, McGinnis TM, Chen PP, Hong X, Jarvo ER. Nickel-Catalyzed Alkyl-Alkyl Cross-Electrophile Coupling Reaction of 1,3-Dimesylates for the Synthesis of Alkylcyclopropanes. Journal of the American Chemical Society. PMID 32129601 DOI: 10.1021/Jacs.0C01330 |
0.637 |
|
2020 |
Dawson DD, Oswald VF, Borovik AS, Jarvo ER. Identification of the Active Catalyst for Nickel-Catalyzed Stereospecific Kumada Coupling Reactions of Ethers. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31953874 DOI: 10.1002/Chem.202000215 |
0.533 |
|
2019 |
Lucas EL, Hewitt KA, Chen PP, Castro AJ, Hong X, Jarvo ER. Engaging Sulfonamides: Intramolecular Cross-Electrophile Coupling Reaction of Sulfonamides with Alkyl Chlorides. The Journal of Organic Chemistry. PMID 31840511 DOI: 10.1021/Acs.Joc.9B02603 |
0.634 |
|
2019 |
Chen PP, Lucas EL, Greene MA, Zhang SQ, Tollefson EJ, Erickson LW, Taylor BLH, Jarvo ER, Hong X. A Unified Explanation for Chemoselectivity and Stereospecificity of Ni-Catalyzed Kumada and Cross-Electrophile Coupling Reactions of Benzylic Ethers: A Combined Computational and Experimental Study. Journal of the American Chemical Society. PMID 30866626 DOI: 10.1021/Jacs.9B00097 |
0.829 |
|
2019 |
Shugrue CR, Sculimbrene BR, Jarvo ER, Mercado BQ, Miller SJ. Outer-Sphere Control for Divergent Multicatalysis with Common Catalytic Moieties. The Journal of Organic Chemistry. PMID 30608173 DOI: 10.1021/Acs.Joc.8B03068 |
0.834 |
|
2019 |
Sanford AB, Tollefson EJ, Jarvo ER. Stereospecific Cross‐Coupling Reactions Provide Conformationally‐Biased Arylalkanes with Anti‐Leukemia Activity Israel Journal of Chemistry. 60: 402-405. DOI: 10.1002/Ijch.201900071 |
0.837 |
|
2018 |
Lucas EL, Jarvo ER. Keeping Track of the Electrons. Accounts of Chemical Research. PMID 29364644 DOI: 10.1021/Acs.Accounts.7B00432 |
0.524 |
|
2018 |
Hanna LE, Konev MO, Jarvo ER. Nickel-Catalyzed Directed Hydroarylation of Alkynes with Boronic Acids European Journal of Organic Chemistry. 2019: 184-187. DOI: 10.1002/Ejoc.201801494 |
0.397 |
|
2017 |
Hanna LE, Harris MR, Domon K, Jarvo ER. Nickel-Catalyzed Hydrogenolysis and Conjugate Addition of 2-(Hydroxymethyl)pyridines via Organozinc Intermediates. Organic Letters. PMID 29135261 DOI: 10.1021/Acs.Orglett.7B03049 |
0.533 |
|
2017 |
Zhang S, Taylor BLH, Ji CL, Gao Y, Harris MR, Hanna LE, Jarvo ER, Houk KN, Hong X. Mechanism and Origins of Ligand-controlled Stereoselectivity of Ni-Catalyzed Suzuki-Miyaura Coupling with Benzylic Esters: A Computational Study. Journal of the American Chemical Society. PMID 28838241 DOI: 10.1021/Jacs.7B04973 |
0.48 |
|
2017 |
Konev MO, Jarvo ER. Nitroxyl Surprise: A Simple Amine Additive Revealed as Copper's Co-Catalyst in the Aerobic Oxidation of Alcohols. Acs Central Science. 3: 272-274. PMID 28470042 DOI: 10.1021/Acscentsci.7B00138 |
0.463 |
|
2017 |
Lucas EL, Jarvo ER. Stereospecific and stereoconvergent cross-couplings between alkyl electrophiles Nature Reviews Chemistry. 1. DOI: 10.1038/S41570-017-0065 |
0.302 |
|
2016 |
Erickson LW, Lucas EL, Tollefson EJ, Jarvo ER. Nickel-Catalyzed Cross-Electrophile Coupling of Alkyl Fluorides: Stereospecific Synthesis of Vinylcyclopropanes. Journal of the American Chemical Society. PMID 27706939 DOI: 10.1021/Jacs.6B07567 |
0.864 |
|
2016 |
Konev MO, Jarvo ER. Decarboxylative Alkyl-Alkyl Cross-Coupling Reactions. Angewandte Chemie (International Ed. in English). PMID 27417297 DOI: 10.1002/Anie.201605593 |
0.604 |
|
2016 |
Konev MO, Hanna LE, Jarvo ER. Intra- and Intermolecular Nickel-Catalyzed Reductive Cross-Electrophile Coupling Reactions of Benzylic Esters with Aryl Halides. Angewandte Chemie (International Ed. in English). PMID 27099968 DOI: 10.1002/Anie.201601206 |
0.64 |
|
2016 |
Konev MO, Jarvo ER. ChemInform Abstract: Decarboxylative Alkyl-Alkyl Cross-Coupling Reactions Cheminform. 47. DOI: 10.1002/CHIN.201644208 |
0.514 |
|
2016 |
Konev MO, Jarvo ER. Decarboxylierende Alkyl-Alkyl-Kreuzkupplungen Angewandte Chemie. 128: 11510-11512. DOI: 10.1002/Ange.201605593 |
0.461 |
|
2015 |
Dawson DD, Jarvo ER. Stereospecific Nickel-Catalyzed Cross-Coupling Reactions of Benzylic Ethers with Isotopically-Labeled Grignard Reagents. Organic Process Research & Development. 19: 1356-1359. PMID 27458328 DOI: 10.1021/Acs.Oprd.5B00148 |
0.629 |
|
2015 |
Hanna LE, Jarvo ER. Selective Cross-Electrophile Coupling by Dual Catalysis. Angewandte Chemie (International Ed. in English). PMID 26630649 DOI: 10.1002/Anie.201509444 |
0.544 |
|
2015 |
Osborne CA, Endean TB, Jarvo ER. Silver-Catalyzed Enantioselective Propargylation Reactions of N-Sulfonylketimines. Organic Letters. 17: 5340-3. PMID 26506430 DOI: 10.1021/Acs.Orglett.5B02692 |
0.649 |
|
2015 |
Tollefson EJ, Erickson LW, Jarvo ER. Stereospecific Intramolecular Reductive Cross-Electrophile Coupling Reactions for Cyclopropane Synthesis. Journal of the American Chemical Society. 137: 9760-3. PMID 26230365 DOI: 10.1021/Jacs.5B03870 |
0.871 |
|
2015 |
Tollefson EJ, Hanna LE, Jarvo ER. Stereospecific nickel-catalyzed cross-coupling reactions of benzylic ethers and esters. Accounts of Chemical Research. 48: 2344-53. PMID 26197033 DOI: 10.1021/Acs.Accounts.5B00223 |
0.88 |
|
2015 |
Johnson AG, Tranquilli MM, Harris MR, Jarvo ER. Selective synthesis of either enantiomer of an anti-breast cancer agent via a common enantioenriched intermediate. Tetrahedron Letters. 56: 3486-3488. PMID 26085695 DOI: 10.1016/J.Tetlet.2015.02.121 |
0.481 |
|
2015 |
Dawson DD, Jarvo ER. Stereospecific nickel-catalyzed cross-coupling reactions of benzylic ethers with isotopically-labeled grignard reagents Organic Process Research and Development. 19: 1356-1359. DOI: 10.1021/acs.oprd.5b00148 |
0.482 |
|
2014 |
Tollefson EJ, Dawson DD, Osborne CA, Jarvo ER. Stereospecific cross-coupling reactions of aryl-substituted tetrahydrofurans, tetrahydropyrans, and lactones. Journal of the American Chemical Society. 136: 14951-8. PMID 25308512 DOI: 10.1021/Ja5076426 |
0.85 |
|
2014 |
Harris MR, Konev MO, Jarvo ER. Enantiospecific intramolecular Heck reactions of secondary benzylic ethers. Journal of the American Chemical Society. 136: 7825-8. PMID 24852707 DOI: 10.1021/Ja5026485 |
0.63 |
|
2014 |
Yonova IM, Osborne CA, Morrissette NS, Jarvo ER. Diaryl and heteroaryl sulfides: synthesis via sulfenyl chlorides and evaluation as selective anti-breast-cancer agents. The Journal of Organic Chemistry. 79: 1947-53. PMID 24564865 DOI: 10.1021/Jo402586V |
0.714 |
|
2014 |
Yonova IM, Johnson AG, Osborne CA, Moore CE, Morrissette NS, Jarvo ER. Stereospecific nickel-catalyzed cross-coupling reactions of alkyl Grignard reagents and identification of selective anti-breast-cancer agents. Angewandte Chemie (International Ed. in English). 53: 2422-7. PMID 24478275 DOI: 10.1002/Anie.201308666 |
0.761 |
|
2014 |
Wisniewska HM, Jarvo ER. Correction to Enantioselective Propargylation and Allenylation Reactions of Ketones and Imines The Journal of Organic Chemistry. 79: 8505-8505. DOI: 10.1021/Jo501820Y |
0.859 |
|
2013 |
Wisniewska HM, Jarvo ER. Enantioselective propargylation and allenylation reactions of ketones and imines. The Journal of Organic Chemistry. 78: 11629-36. PMID 24266761 DOI: 10.1021/Jo4019107 |
0.856 |
|
2013 |
Swift EC, Jarvo ER. Asymmetric transition metal-catalyzed cross-coupling reactions for the construction of tertiary stereocenters. Tetrahedron. 69: 5799-5817. PMID 23956470 DOI: 10.1016/J.Tet.2013.05.001 |
0.86 |
|
2013 |
Wisniewska HM, Swift EC, Jarvo ER. Functional-group-tolerant, nickel-catalyzed cross-coupling reaction for enantioselective construction of tertiary methyl-bearing stereocenters. Journal of the American Chemical Society. 135: 9083-90. PMID 23751004 DOI: 10.1021/Ja4034999 |
0.841 |
|
2013 |
Kohn BL, Ichiishi N, Jarvo ER. Silver-catalyzed allenylation and enantioselective propargylation reactions of ketones. Angewandte Chemie (International Ed. in English). 52: 4414-7. PMID 23495207 DOI: 10.1002/Anie.201206971 |
0.867 |
|
2013 |
Harris MR, Hanna LE, Greene MA, Moore CE, Jarvo ER. Retention or inversion in stereospecific nickel-catalyzed cross-coupling of benzylic carbamates with arylboronic esters: control of absolute stereochemistry with an achiral catalyst. Journal of the American Chemical Society. 135: 3303-6. PMID 23414579 DOI: 10.1021/Ja311783K |
0.751 |
|
2013 |
Swift EC, Jarvo ER. Corrigendum to “Asymmetric transition metal-catalyzed cross-coupling reactions for the construction of tertiary stereocenters” [Tetrahedron 69 (2013) 5719–5817] Tetrahedron. 69: 7157. DOI: 10.1016/J.Tet.2013.06.090 |
0.807 |
|
2012 |
Taylor BL, Harris MR, Jarvo ER. Synthesis of enantioenriched triarylmethanes by stereospecific cross-coupling reactions. Angewandte Chemie (International Ed. in English). 51: 7790-3. PMID 22740234 DOI: 10.1002/Anie.201202527 |
0.75 |
|
2012 |
Greene MA, Yonova IM, Williams FJ, Jarvo ER. Traceless directing group for stereospecific nickel-catalyzed alkyl-alkyl cross-coupling reactions. Organic Letters. 14: 4293-6. PMID 22568515 DOI: 10.1021/Ol300891K |
0.841 |
|
2012 |
Williams FJ, Grote RE, Jarvo ER. Rhodium-catalyzed redox allylation reactions of ketones. Chemical Communications (Cambridge, England). 48: 1496-8. PMID 21984365 DOI: 10.1039/C1Cc14691B |
0.862 |
|
2011 |
Barczak NT, Jarvo ER. Regioselective silver-mediated Kondakov-Darzens olefin acylation. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 12912-6. PMID 22006828 DOI: 10.1002/Chem.201102476 |
0.448 |
|
2011 |
Shaghafi MB, Grote RE, Jarvo ER. Oxazolidine synthesis by complementary stereospecific and stereoconvergent methods. Organic Letters. 13: 5188-91. PMID 21866944 DOI: 10.1021/Ol202068P |
0.833 |
|
2011 |
Kohn BL, Jarvo ER. Palladium-catalyzed annulation reactions for diastereoselective cyclopentene synthesis. Organic Letters. 13: 4858-61. PMID 21854011 DOI: 10.1021/Ol2019423 |
0.863 |
|
2011 |
Taylor BL, Jarvo ER. Stereochemistry of transmetalation of alkylboranes in nickel-catalyzed alkyl-alkyl cross-coupling reactions. The Journal of Organic Chemistry. 76: 7573-6. PMID 21797268 DOI: 10.1021/Jo201263R |
0.7 |
|
2011 |
Barker TJ, Jarvo ER. Titanium-mediated amination of Grignard reagents using primary and secondary amines. Angewandte Chemie (International Ed. in English). 50: 8325-8. PMID 21770007 DOI: 10.1002/Anie.201103700 |
0.708 |
|
2011 |
Williams FJ, Jarvo ER. Palladium-catalyzed cascade reaction for the synthesis of substituted isoindolines. Angewandte Chemie (International Ed. in English). 50: 4459-62. PMID 21480447 DOI: 10.1002/Anie.201008160 |
0.787 |
|
2011 |
Taylor BL, Swift EC, Waetzig JD, Jarvo ER. Stereospecific nickel-catalyzed cross-coupling reactions of alkyl ethers: enantioselective synthesis of diarylethanes. Journal of the American Chemical Society. 133: 389-91. PMID 21155567 DOI: 10.1021/Ja108547U |
0.884 |
|
2011 |
Taylor BLH, Jarvo ER. Construction of enantioenriched tertiary stereogenic centers by nickel- and palladium-catalyzed cross-coupling reactions of alkyl electrophiles Synlett. 2761-2765. DOI: 10.1055/S-0031-1289871 |
0.552 |
|
2011 |
Barker TJ, Jarvo ER. Developments in transition-metal-catalyzed reactions using electrophilic nitrogen sources Synthesis. 3954-3964. DOI: 10.1055/S-0031-1289581 |
0.709 |
|
2011 |
Wisniewska HM, Jarvo ER. Enantioselective silver-catalyzed propargylation of imines Chemical Science. 2: 807-810. DOI: 10.1039/C0Sc00613K |
0.839 |
|
2010 |
Barker TJ, Jarvo ER. Diene-ligated iridium complexes as catalysts for allylation and methallylation reactions of ketones Synthesis. 3259-3262. DOI: 10.1055/S-0030-1258196 |
0.812 |
|
2009 |
Barker TJ, Jarvo ER. Umpolung amination: nickel-catalyzed coupling reactions of N,N-dialkyl-N-chloroamines with diorganozinc reagents. Journal of the American Chemical Society. 131: 15598-9. PMID 19824677 DOI: 10.1021/Ja907038B |
0.697 |
|
2009 |
Barker TJ, Jarvo ER. Diene-ligated iridium catalyst for allylation reactions of ketones and imines. Organic Letters. 11: 1047-9. PMID 19196013 DOI: 10.1021/Ol802598C |
0.817 |
|
2009 |
Grote RE, Jarvo ER. Palladium-catalyzed, one-pot, three-component synthesis of homoallylic amines from aldehydes, anisidine, and allyl trifluoroacetate. Organic Letters. 11: 485-8. PMID 19093851 DOI: 10.1021/Ol8026297 |
0.869 |
|
2009 |
Waetzig JD, Swift EC, Jarvo ER. Conjugate allylation reactions of alkylidene malononitriles mediated by NHC-ligated palladium catalysts Tetrahedron. 65: 3197-3201. DOI: 10.1016/J.Tet.2008.10.061 |
0.859 |
|
2009 |
Shaghafi MB, Kohn BL, Jarvo ER. ChemInform Abstract: Palladium-Catalyzed Conjugate Allylation Reactions of α,β-Unsaturated N-Acylpyrroles. Cheminform. 40. DOI: 10.1002/chin.200912124 |
0.803 |
|
2008 |
Shaghafi MB, Kohn BL, Jarvo ER. Palladium-catalyzed conjugate allylation reactions of alpha,beta-unsaturated N-acylpyrroles. Organic Letters. 10: 4743-6. PMID 18828594 DOI: 10.1021/Ol801830H |
0.813 |
|
2008 |
Barczak NT, Jarvo ER. Silver-catalyzed, manganese-mediated allylation and benzylation reactions of aldehydes and ketones European Journal of Organic Chemistry. 5507-5510. DOI: 10.1002/Ejoc.200800898 |
0.601 |
|
2007 |
Barczak NT, Grote RE, Jarvo ER. Catalytic umpolung allylation of aldehydes by π-allylpalladium complexes containing bidentate N-heterocyclic carbene ligands Organometallics. 26: 4863-4865. DOI: 10.1021/Om700605Y |
0.833 |
|
2005 |
Jarvo ER, Lawrence BM, Jacobsen EN. Highly enantio- and regioselective quinone Diels-Alder reactions catalyzed by a tridentate [(Schiff Base)Cr(III)] complex. Angewandte Chemie (International Ed. in English). 44: 6043-6. PMID 16134190 DOI: 10.1002/Anie.200502176 |
0.754 |
|
2005 |
Boezio AA, Jarvo ER, Lawrence BM, Jacobsen EN. Efficient total syntheses of (-)-colombiasin A and (-)-elisapterosin B: application of the Cr-catalyzed asymmetric quinone Diels-Alder reaction. Angewandte Chemie (International Ed. in English). 44: 6046-50. PMID 16108082 DOI: 10.1002/Anie.200502178 |
0.829 |
|
2002 |
Jarvo ER, Miller SJ. Amino acids and peptides as asymmetric organocatalysts Tetrahedron. 58: 2481-2495. DOI: 10.1016/S0040-4020(02)00122-9 |
0.389 |
|
2001 |
Vasbinder MM, Jarvo ER, Miller SJ. Incorporation of Peptide Isosteres into Enantioselective Peptide-Based Catalysts as Mechanistic Probes. Angewandte Chemie (International Ed. in English). 40: 2824-2827. PMID 29711981 DOI: 10.1002/1521-3773(20010803)40:15<2824::Aid-Anie2824>3.0.Co;2-J |
0.766 |
|
2001 |
Vasbinder MM, Jarvo ER, Miller SJ. Incorporation of Peptide Isosteres into Enantioselective Peptide-Based Catalysts as Mechanistic Probes This research is supported by the U.S. National Science Foundation (CHE-9874963). We are also grateful to the U.S. NIH (GM-57595), DuPont, Eli Lilly, Glaxo-Wellcome, and Merck for research support. S.J.M. is a Fellow of the Alfred P. Sloan Foundation, a Cottrell Scholar of Research Corporation, and a Camille Dreyfus Teacher-Scholar. Angewandte Chemie (International Ed. in English). 40: 2824-2827. PMID 11500878 DOI: 10.1002/1521-3773(20010803)40:15<2824::Aid-Anie2824>3.3.Co;2-A |
0.721 |
|
2001 |
Jarvo ER, Evans CA, Copeland GT, Miller SJ. Fluorescence-based screening of asymmetric acylation catalysts through parallel enantiomer analysis. Identification of a catalyst for tertiary alcohol resolution. The Journal of Organic Chemistry. 66: 5522-7. PMID 11485477 DOI: 10.1021/Jo015803Z |
0.787 |
|
2000 |
Jarvo ER, Vasbinder MM, Miller SJ. Asymmetric acylation reactions catalyzed by conformationally biased octapeptides Tetrahedron. 56: 9773-9779. |
0.832 |
|
1999 |
Jarvo ER, Copeland GT, Papaioannou N, Bonitatebus PJ, Miller SJ. A biomimetic approach to asymmetric acyl transfer catalysis Journal of the American Chemical Society. 121: 11638-11643. DOI: 10.1021/Ja9931776 |
0.806 |
|
1998 |
Copeland GT, Jarvo ER, Miller SJ. Minimal Acylase-Like Peptides. Conformational Control of Absolute Stereospecificity. The Journal of Organic Chemistry. 63: 6784-6785. PMID 11672295 DOI: 10.1021/Jo981642W |
0.747 |
|
1996 |
Jarvo ER, Boothroyd SR, Kerr MA. The High Pressure Diels-Alder Reactions of Quinone-mono-ketals Synlett. 1996: 897-899. DOI: 10.1055/S-1996-5615 |
0.351 |
|
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