Year |
Citation |
Score |
2022 |
Liu J, Lorraine SC, Dolinar BS, Hoover JM. Aerobic Oxidation Reactivity of Well-Defined Cobalt(II) and Cobalt(III) Aminophenol Complexes. Inorganic Chemistry. 61: 6008-6016. PMID 35414172 DOI: 10.1021/acs.inorgchem.1c03686 |
0.362 |
|
2020 |
Liu J, Morgan S, Hoover JM. Cobalt‐Catalyzed Aerobic Oxidative Cyclization of 2‐Aminoanilines with Isonitriles: Facile Access to 2‐Aminobenzimidazoles Chemcatchem. 12: 1297-1301. DOI: 10.1002/Cctc.201902011 |
0.399 |
|
2019 |
Liu J, Hoover JM. Cobalt-Catalyzed Aerobic Oxidative Cyclization of 2-Aminophenols with Isonitriles: 2-Aminophenol Enabled O Activation by Cobalt(II). Organic Letters. PMID 31184180 DOI: 10.1021/Acs.Orglett.9B01384 |
0.451 |
|
2019 |
Green K, Hoover JM. Intermediacy of Copper(I) under Oxidative Conditions in the Aerobic Copper-Catalyzed Decarboxylative Thiolation of Benzoic Acids Acs Catalysis. 10: 1769-1782. DOI: 10.1021/Acscatal.9B04110 |
0.463 |
|
2018 |
Honeycutt AP, Hoover JM. Nickel-Catalyzed Oxidative Decarboxylative Annulation for the Synthesis of Heterocycle-Containing Phenanthridinones. Organic Letters. 20: 7216-7219. PMID 30394749 DOI: 10.1021/Acs.Orglett.8B03144 |
0.443 |
|
2018 |
Crovak RA, Hoover JM. A Predictive Model for the Decarboxylation of Silver Benzoate Complexes Relevant to Decarboxylative Coupling Reactions. Journal of the American Chemical Society. PMID 29381354 DOI: 10.1021/Jacs.7B13305 |
0.327 |
|
2017 |
Li M, Petersen JL, Hoover JM. Silver-Mediated Oxidative Decarboxylative Trifluoromethylthiolation of Coumarin-3-carboxylic Acids. Organic Letters. PMID 28111954 DOI: 10.1021/Acs.Orglett.6B03806 |
0.354 |
|
2017 |
Baur A, Bustin KA, Aguilera E, Petersen JL, Hoover JM. Copper and silver benzoate and aryl complexes and their implications for oxidative decarboxylative coupling reactions Organic Chemistry Frontiers. 4: 519-524. DOI: 10.1039/C6Qo00678G |
0.468 |
|
2017 |
Honeycutt AP, Hoover JM. Nickel-Catalyzed Oxidative Decarboxylative (Hetero)Arylation of Unactivated C–H Bonds: Ni and Ag Synergy Acs Catalysis. 7: 4597-4601. DOI: 10.1021/Acscatal.7B01683 |
0.469 |
|
2016 |
Hoover J. Ammonia activation at a metal Science. 354: 707-708. PMID 27846593 DOI: 10.1126/Science.Aaj2332 |
0.363 |
|
2016 |
Li M, Hoover JM. Aerobic copper-catalyzed decarboxylative thiolation. Chemical Communications (Cambridge, England). PMID 27334832 DOI: 10.1039/C6Cc04486G |
0.377 |
|
2016 |
Hoover JM. Mechanistic Aspects of Copper-Catalyzed Decarboxylative Coupling Reactions of (Hetero)Aryl Carboxylic Acids Comments On Inorganic Chemistry. 37: 169-200. DOI: 10.1080/02603594.2016.1261023 |
0.419 |
|
2016 |
Gowda AS, Baur A, Scaggs CA, Petersen JL, Hoover JM. Formation of Di-tert-butylurea from a Mononuclear Iron Tris(isocyanide) Complex Organometallics. 35: 3720-3727. DOI: 10.1021/Acs.Organomet.6B00687 |
0.314 |
|
2015 |
Chen L, Ju L, Bustin KA, Hoover JM. Copper-catalyzed oxidative decarboxylative C-H arylation of benzoxazoles with 2-nitrobenzoic acids. Chemical Communications (Cambridge, England). 51: 15059-62. PMID 26314336 DOI: 10.1039/C5Cc06645J |
0.412 |
|
2014 |
Hoover JM, Stahl SS. Air Oxidation of Primary Alcohols Catalyzed by Copper(I)/TEMPO. Preparation of 2‐Amino‐5‐bromo‐benzaldehyde Organic Syntheses. 240-250. DOI: 10.1002/0471264229.Os090.23 |
0.601 |
|
2013 |
Hoover JM, Ryland BL, Stahl SS. Copper/TEMPO-Catalyzed Aerobic Alcohol Oxidation: Mechanistic Assessment of Different Catalyst Systems. Acs Catalysis. 3: 2599-2605. PMID 24558634 DOI: 10.1021/Cs400689A |
0.734 |
|
2013 |
Hoover JM, Ryland BL, Stahl SS. Mechanism of copper(I)/TEMPO-catalyzed aerobic alcohol oxidation. Journal of the American Chemical Society. 135: 2357-67. PMID 23317450 DOI: 10.1021/Ja3117203 |
0.739 |
|
2013 |
Hoover JM, Stahl SS. Air oxidation of primary alcohols catalyzed by copper(I)/TEMPO. Preparation of 2-amino-5-bromobenzaldehyde Organic Syntheses. 90: 240-250. DOI: 10.15227/orgsyn.090.0240 |
0.522 |
|
2013 |
Greene JF, Hoover JM, Mannel DS, Root TW, Stahl SS. Continuous-flow aerobic oxidation of primary alcohols with a copper(I)/TEMPO catalyst Organic Process Research and Development. 17: 1247-1251. DOI: 10.1021/Op400207F |
0.747 |
|
2013 |
Hill NJ, Hoover JM, Stahl SS. Aerobic alcohol oxidation using a copper(I)/TEMPO catalyst system: A green, catalytic oxidation reaction for the undergraduate organic chemistry laboratory Journal of Chemical Education. 90: 102-105. DOI: 10.1021/Ed300368Q |
0.581 |
|
2012 |
Hoover JM, Steves JE, Stahl SS. Copper(I)/TEMPO-catalyzed aerobic oxidation of primary alcohols to aldehydes with ambient air. Nature Protocols. 7: 1161-6. PMID 22635108 DOI: 10.1038/Nprot.2012.057 |
0.635 |
|
2011 |
Hoover JM, Stahl SS. Highly practical copper(I)/TEMPO catalyst system for chemoselective aerobic oxidation of primary alcohols. Journal of the American Chemical Society. 133: 16901-10. PMID 21861488 DOI: 10.1021/Ja206230H |
0.651 |
|
2010 |
Hoover JM, Dipasquale A, Mayer JM, Michael FE. Platinum-catalyzed intramolecular hydrohydrazination: evidence for alkene insertion into a Pt-N bond. Journal of the American Chemical Society. 132: 5043-53. PMID 20334376 DOI: 10.1021/Ja906563Z |
0.721 |
|
2008 |
Hoover JM, Freudenthal J, Michael FE, Mayer JM. Reactivity of low-valent iridium, rhodium, and platinum complexes with Di- and tetrasubstituted hydrazines Organometallics. 27: 2238-2245. DOI: 10.1021/Om701192S |
0.703 |
|
2007 |
Hoover JM, DiPasquale A, Mayer JM, Michael FE. Synthesis and reactivity of a ruthenium(III) bis(anilide) dimer by oxidative addition of an N,N′-disubstituted hydrazine Organometallics. 26: 3297-3305. DOI: 10.1021/Om0700462 |
0.688 |
|
2005 |
Petersen JR, Hoover JM, Kassel WS, Rheingold AL, Johnson AR. Titanium complexes with chiral amino alcohol ligands: Synthesis and structure of complexes related to hydroamination catalysts Inorganica Chimica Acta. 358: 687-694. DOI: 10.1016/J.Ica.2004.09.051 |
0.43 |
|
2004 |
Hoover JM, Petersen JR, Pikul JH, Johnson AR. Catalytic intramolecular hydroamination of substituted aminoallenes by chiral titanium amino-alcohol complexes Organometallics. 23: 4614-4620. DOI: 10.1021/Om049564S |
0.523 |
|
Show low-probability matches. |