Year |
Citation |
Score |
2024 |
Ho AT, Vanable EP, Miguel CS, Hull KL. Iridium-catalysed hydroamination of internal homoallylic amines. Chemical Communications (Cambridge, England). PMID 38230687 DOI: 10.1039/d3cc05594a |
0.43 |
|
2024 |
Wendlandt HC, Trammel GL, Kohler DG, Utley JA, Nicely AM, Popov AG, Hull KL. Copper-Catalyzed Three-Component Carboiminolactonization of Electron-Deficient Olefins. The Journal of Organic Chemistry. PMID 38198512 DOI: 10.1021/acs.joc.3c02326 |
0.417 |
|
2023 |
Ho TD, Lee BJ, Tan C, Utley JA, Ngo NQ, Hull KL. Efficient Synthesis of α-Haloboronic Esters via Cu-Catalyzed Atom Transfer Radical Addition. Journal of the American Chemical Society. PMID 38054923 DOI: 10.1021/jacs.3c11347 |
0.373 |
|
2023 |
Gay BL, Wang YN, Bhatt S, Tarasewicz A, Cooke DJ, Milem EG, Zhang B, Gary JB, Neidig ML, Hull KL. Palladium and Iron Cocatalyzed Aerobic Alkene Aminoboration. Journal of the American Chemical Society. PMID 37584107 DOI: 10.1021/jacs.3c05790 |
0.307 |
|
2023 |
Nicely AM, Popov AG, Wendlandt HC, Trammel GL, Kohler DG, Hull KL. Cu-Catalyzed Three-Component Carboamination of Electron Deficient Olefins. Organic Letters. 25: 5302-5307. PMID 37440170 DOI: 10.1021/acs.orglett.3c01866 |
0.476 |
|
2022 |
Ho AT, Ensign SC, Vanable EP, Portillo D, Humke JN, Kortman GD, Hull KL. Rhodium-/Iridium-Catalyzed Hydroamination for the Synthesis of 1,2-, 1,3-, or 1,4-Diamines. Acs Catalysis. 12: 8331-8340. PMID 37143789 DOI: 10.1021/acscatal.2c01835 |
0.461 |
|
2022 |
Bhatt S, Wang YN, Pham HTP, Hull KL. Palladium-Catalyzed Oxidative Amination of α-Olefins with Indoles. Organic Letters. PMID 35905441 DOI: 10.1021/acs.orglett.2c02190 |
0.443 |
|
2022 |
Lee BJ, Ickes AR, Gupta AK, Ensign SC, Ho TD, Tarasewicz A, Vanable EP, Kortman GD, Hull KL. Synthesis of Unsymmetrical Vicinal Diamines via Directed Hydroamination. Organic Letters. PMID 35862860 DOI: 10.1021/acs.orglett.2c01911 |
0.543 |
|
2021 |
Gockel SN, Lee S, Gay BL, Hull KL. Oxidative Three-Component Carboamination of Vinylarenes with Alkylboronic Acids. Acs Catalysis. 11: 5166-5171. PMID 36619299 DOI: 10.1021/acscatal.1c00105 |
0.347 |
|
2021 |
Wu Z, Gockel SN, Hull KL. Anti-Markovnikov hydro(amino)alkylation of vinylarenes via photoredox catalysis. Nature Communications. 12: 5956. PMID 34642311 DOI: 10.1038/s41467-021-26170-6 |
0.375 |
|
2021 |
Buchanan TL, Gockel SN, Veatch AM, Wang YN, Hull KL. Copper-Catalyzed Three-Component Alkene Carbofunctionalization: C-N, C-O, and C-C Bond Formation from a Single Reaction Platform. Organic Letters. PMID 34096733 DOI: 10.1021/acs.orglett.1c01180 |
0.75 |
|
2021 |
Gockel SN, Buchanan TL, Hull KL. Correction to "Cu-Catalyzed Three-Component Carboamination of Alkenes". Journal of the American Chemical Society. 143: 6019-6020. PMID 33821635 DOI: 10.1021/jacs.1c03077 |
0.706 |
|
2019 |
Qi X, Kohler DG, Hull KL, Liu P. Energy Decomposition Analyses Reveal the Origins of Catalyst and Nucleophile Effects on Regioselectivity in Nucleopalladation of Alkenes. Journal of the American Chemical Society. PMID 31322875 DOI: 10.1021/Jacs.9B02893 |
0.363 |
|
2019 |
Trost BM, Nagaraju A, Wang F, Zuo Z, Xu J, Hull KL. Palladium-Catalyzed Decarboxylative Asymmetric Allylic Alkylation of Dihydroquinolinones. Organic Letters. PMID 30834753 DOI: 10.1021/Acs.Orglett.9B00358 |
0.753 |
|
2019 |
Vanable EP, Kennemur JL, Joyce LA, Ruck RT, Schultz DM, Hull KL. Rhodium-Catalyzed Asymmetric Hydroamination of Allyl Amines. Journal of the American Chemical Society. PMID 30614700 DOI: 10.1021/Jacs.8B09811 |
0.491 |
|
2018 |
Laffoon SD, Wu Z, Hull KL. Rhodium-catalyzed asymmetric synthesis of β-branched esters from allylic amines. Chemical Communications (Cambridge, England). PMID 29946625 DOI: 10.1039/C8Cc02612B |
0.454 |
|
2018 |
Wu Z, Laffoon SD, Hull KL. Asymmetric synthesis of γ-branched amines via rhodium-catalyzed reductive amination. Nature Communications. 9: 1185. PMID 29567989 DOI: 10.1038/S41467-018-03535-Y |
0.482 |
|
2018 |
Kohler DG, Gockel SN, Kennemur JL, Waller PJ, Hull KL. Palladium-catalysed anti-Markovnikov selective oxidative amination. Nature Chemistry. 10: 333-340. PMID 29461537 DOI: 10.1038/Nchem.2904 |
0.524 |
|
2017 |
Gockel SN, Buchanan TL, Hull KL. Cu-Catalyzed Three-Component Carboamination of Alkenes. Journal of the American Chemical Society. PMID 29095598 DOI: 10.1021/Jacs.7B10529 |
0.748 |
|
2017 |
Buchanan TL, Hull KL. Illuminating amination. Science (New York, N.Y.). 355: 690-691. PMID 28209858 DOI: 10.1126/science.aam6382 |
0.723 |
|
2017 |
Yamamoto H, Shimoda Y, Wu Z, Laffoon SD, Nguyen TT, McAlpin JD, Hull KL. Rhodium-Catalyzed Asymmetric Synthesis of Amides Synfacts. 13: 399-1375. DOI: 10.1055/S-0036-1590147 |
0.519 |
|
2017 |
Kortman GD, Hull KL. Copper-Catalyzed Hydroarylation of Internal Alkynes: Highly Regio- and Diastereoselective Synthesis of 1,1-Diaryl, Trisubstituted Olefins Acs Catalysis. 7: 6220-6224. DOI: 10.1021/Acscatal.7B01847 |
0.551 |
|
2016 |
Wu Z, Hull KL. Rhodium-catalyzed oxidative amidation of allylic alcohols and aldehydes: effective conversion of amines and anilines into amides. Chemical Science. 7: 969-975. PMID 29896367 DOI: 10.1039/C5Sc03103F |
0.413 |
|
2016 |
Wu Z, Laffoon SD, Nguyen TT, McAlpin JD, Hull KL. Rhodium-Catalyzed Asymmetric Synthesis of β-Branched Amides. Angewandte Chemie (International Ed. in English). PMID 28026091 DOI: 10.1002/Anie.201610500 |
0.408 |
|
2016 |
Trost BM, Stivala CE, Fandrick DR, Hull KL, Huang A, Poock C, Kalkofen R. Total Synthesis of (-)-Lasonolide A. Journal of the American Chemical Society. PMID 27548113 DOI: 10.1021/Jacs.6B05127 |
0.703 |
|
2016 |
Kennemur JL, Kortman GD, Hull KL. Rhodium-Catalyzed Regiodivergent Hydrothiolation of Allyl Amines and Imines. Journal of the American Chemical Society. PMID 27547858 DOI: 10.1021/Jacs.6B07142 |
0.417 |
|
2016 |
Wu Z, Hull KL. Rhodium-catalyzed oxidative amidation of allylic alcohols and aldehydes: Effective conversion of amines and anilines into amides Chemical Science. 7: 969-975. DOI: 10.1039/c5sc03103f |
0.306 |
|
2016 |
Nguyen TT, Hull KL. Rhodium-Catalyzed Oxidative Amidation of Sterically Hindered Aldehydes and Alcohols Acs Catalysis. 6: 8214-8218. DOI: 10.1021/Acscatal.6B02541 |
0.489 |
|
2016 |
Nguyen TT, Kortman GD, Hull KL. Synthesis, Cycloaddition, and Cycloreversion Reactions of Mononuclear Titanocene-oxo Complexes Organometallics. 35: 1713-1725. DOI: 10.1021/Acs.Organomet.6B00111 |
0.43 |
|
2015 |
Ensign SC, Vanable EP, Kortman GD, Weir LJ, Hull KL. Anti-Markovnikov Hydroamination of Homoallylic Amines. Journal of the American Chemical Society. 137: 13748-51. PMID 26456593 DOI: 10.1021/Jacs.5B08500 |
0.467 |
|
2015 |
Gockel SN, Hull KL. Chloroform as a Carbon Monoxide Precursor: In or Ex Situ Generation of CO for Pd-Catalyzed Aminocarbonylations. Organic Letters. 17: 3236-9. PMID 26090688 DOI: 10.1021/Acs.Orglett.5B01385 |
0.492 |
|
2015 |
Gupta AK, Hull KL. Synthesis of 1,2-Diamines via Hydroamination Reactions Synlett. DOI: 10.1055/S-0034-1380750 |
0.61 |
|
2015 |
Kortman GD, Orr MJ, Hull KL. Synthesis and reactivity of dioxazirconacyclohexenes: Development of a zirconium-oxo-mediated alkyne-aldehyde coupling reaction Organometallics. 34: 1013-1016. DOI: 10.1021/Om5008727 |
0.519 |
|
2015 |
Nguyen TT, Bertke JA, Gray DL, Hull KL. Facile C-H, C-F, C-Cl, and C-C Activation by Oxatitanacyclobutene Complexes Organometallics. 34: 4190-4193. DOI: 10.1021/Acs.Organomet.5B00470 |
0.411 |
|
2014 |
Ickes AR, Ensign SC, Gupta AK, Hull KL. Regio- and chemoselective intermolecular hydroamination of allyl imines for the synthesis of 1,2-diamines. Journal of the American Chemical Society. 136: 11256-9. PMID 25050740 DOI: 10.1021/Ja505794U |
0.621 |
|
2014 |
Trost BM, Stivala CE, Hull KL, Huang A, Fandrick DR. A concise synthesis of (-)-lasonolide A. Journal of the American Chemical Society. 136: 88-91. PMID 24308383 DOI: 10.1021/Ja411270D |
0.715 |
|
2014 |
Carreira EM, Jacobsen MJ, Trost BM, Stivala CE, Hull KL, Huang A, Fandrick DR. Synthesis of (–)-Lasonolide A Synfacts. 10: 235-235. DOI: 10.1055/S-0033-1340711 |
0.455 |
|
2014 |
Trost BM, Stivala CE, Hull KL, Huang A, Fandrick DR. ChemInform Abstract: A Concise Synthesis of (-)-Lasonolide A (I). Cheminform. 45: no-no. DOI: 10.1002/chin.201430217 |
0.426 |
|
2011 |
Lyons TW, Hull KL, Sanford MS. Controlling site selectivity in Pd-catalyzed oxidative cross-coupling reactions. Journal of the American Chemical Society. 133: 4455-64. PMID 21381698 DOI: 10.1021/Ja1097918 |
0.594 |
|
2009 |
Hull KL, Sanford MS. Mechanism of benzoquinone-promoted palladium-catalyzed oxidative cross-coupling reactions. Journal of the American Chemical Society. 131: 9651-3. PMID 19569623 DOI: 10.1021/Ja901952H |
0.64 |
|
2007 |
Hull KL, Sanford MS. Catalytic and highly regioselective cross-coupling of aromatic C-H substrates. Journal of the American Chemical Society. 129: 11904-5. PMID 17845047 DOI: 10.1021/Ja074395Z |
0.642 |
|
2006 |
Hull KL, Lanni EL, Sanford MS. Highly regioselective catalytic oxidative coupling reactions: synthetic and mechanistic investigations. Journal of the American Chemical Society. 128: 14047-9. PMID 17061885 DOI: 10.1021/Ja065718E |
0.671 |
|
2006 |
Hull KL, Anani WQ, Sanford MS. Palladium-catalyzed fluorination of carbon-hydrogen bonds. Journal of the American Chemical Society. 128: 7134-5. PMID 16734446 DOI: 10.1021/Ja061943K |
0.644 |
|
2004 |
Desai LV, Hull KL, Sanford MS. Palladium-catalyzed oxygenation of unactivated sp3 C-H bonds. Journal of the American Chemical Society. 126: 9542-3. PMID 15291549 DOI: 10.1021/Ja046831C |
0.636 |
|
2004 |
Dick AR, Hull KL, Sanford MS. A highly selective catalytic method for the oxidative functionalization of C-H bonds. Journal of the American Chemical Society. 126: 2300-1. PMID 14982422 DOI: 10.1021/Ja031543M |
0.749 |
|
2002 |
Mio MJ, Kopel LC, Braun JB, Gadzikwa TL, Hull KL, Brisbois RG, Markworth CJ, Grieco PA. One-pot synthesis of symmetrical and unsymmetrical bisarylethynes by a modification of the sonogashira coupling reaction. Organic Letters. 4: 3199-202. PMID 12227748 DOI: 10.1021/Ol026266N |
0.448 |
|
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