Kenneth Nicholas - Publications

Affiliations: 
Department of Chemistry and Biochemistry University of Oklahoma, Norman, OK, United States 
Area:
Organic Chemistry

66 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2018 Steffensmeier E, Swann MT, Nicholas KM. Mechanistic Features of the Oxidation-Reductive Coupling of Alcohols Catalyzed by Oxo-Vanadium Complexes. Inorganic Chemistry. PMID 30525521 DOI: 10.1021/acs.inorgchem.8b02968  0.321
2015 Boucher-Jacobs C, Nicholas KM. Oxo-Rhenium-Catalyzed Deoxydehydration of Polyols with Hydroaromatic Reductants Organometallics. 34: 1985-1990. DOI: 10.1021/ACS.ORGANOMET.5B00226  0.327
2014 Tran AT, Liu P, Houk KN, Nicholas KM. Regioselectivity in the Cu(I)-catalyzed [4 + 2]-cycloaddition of 2-nitrosopyridine with unsymmetrical dienes. The Journal of Organic Chemistry. 79: 5617-26. PMID 24853468 DOI: 10.1021/Jo5005907  0.37
2013 John A, Byun J, Nicholas KM. Copper-catalyzed C(sp2)-H amidation of unactivated arenes by N-tosyloxycarbamates. Chemical Communications (Cambridge, England). 49: 10965-7. PMID 24132225 DOI: 10.1039/C3Cc46412A  0.757
2013 Chapman G, Nicholas KM. Vanadium-catalyzed deoxydehydration of glycols. Chemical Communications (Cambridge, England). 49: 8199-201. PMID 23925040 DOI: 10.1039/c3cc44656e  0.302
2013 Liu P, Nicholas KM. Mechanism of sulfite-driven, MeReO3-catalyzed deoxydehydration of glycols Organometallics. 32: 1821-1831. DOI: 10.1021/Om301251Z  0.309
2012 John A, Nicholas KM. Palladium catalyzed C-H functionalization of O-arylcarbamates: selective ortho-bromination using NBS. The Journal of Organic Chemistry. 77: 5600-5. PMID 22663545 DOI: 10.1021/Jo300713H  0.756
2012 John A, Nicholas KM. Copper-Mediated Multiple C–H Functionalization of AromaticN-Heterocycles: Bromoamination of Indoles and Pyrroles Organometallics. 31: 7914-7920. DOI: 10.1021/Om300553B  0.702
2012 Stanowski S, Nicholas KM, Srivastava RS. [Cp*Ru(CO)2]2-Catalyzed Hydrodeoxygenation and Hydrocracking of Diols and Epoxides Organometallics. 31: 515-518. DOI: 10.1021/OM200447Z  0.333
2012 Volkman J, Nicholas KM. A synthetic quest for tris(imidazolyl) carboxylates and their metal complexes: Active site models for quercetin 2,3-dioxygenases and other non-heme redox metalloenzymes Tetrahedron. 68: 3368-3376. DOI: 10.1016/J.Tet.2012.02.042  0.611
2011 John A, Nicholas KM. Copper-catalyzed amidation of 2-phenylpyridine with oxygen as the terminal oxidant. The Journal of Organic Chemistry. 76: 4158-62. PMID 21401207 DOI: 10.1021/Jo200409H  0.765
2011 Ahmad I, Chapman G, Nicholas KM. Sulfite-Driven, Oxorhenium-Catalyzed Deoxydehydration of Glycols Organometallics. 30: 2810-2818. DOI: 10.1021/OM2001662  0.318
2011 Kannappan R, Matsumoto M, Hallren J, Nicholas KM. New chiral Schiff base-zinc complexes and their esterolytic catalytic activity Journal of Molecular Catalysis a: Chemical. 339: 72-78. DOI: 10.1016/j.molcata.2011.02.014  0.571
2011 Barman DN, Nicholas KM. Copper-catalyzed intramolecular C-H amination European Journal of Organic Chemistry. 908-911. DOI: 10.1002/Ejoc.201001160  0.781
2011 Barman DN, Nicholas KM. ChemInform Abstract: Copper-Catalyzed Intramolecular C-H Amination. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201122126  0.806
2011 Palmisano G, Penoni A, Sisti M, Tibiletti F, Tollari S, Nicholas KM. ChemInform Abstract: Synthesis of Indole Derivatives with Biological Activity by Reactions Between Unsaturated Hydrocarbons and N-Aromatic Precursors Cheminform. 42: no-no. DOI: 10.1002/CHIN.201113245  0.319
2010 Lamar AA, Nicholas KM. Iodine-catalyzed aminosulfonation of hydrocarbons by imidoiodinanes. A synthetic and mechanistic investigation. The Journal of Organic Chemistry. 75: 7644-50. PMID 20977281 DOI: 10.1021/Jo1015213  0.755
2010 Vkuturi S, Chapman G, Ahmad I, Nicholas KM. Rhenium-catalyzed deoxydehydration of glycols by sulfite. Inorganic Chemistry. 49: 4744-6. PMID 20441161 DOI: 10.1021/ic100467p  0.347
2010 Barman DN, Liu P, Houk KN, Nicholas KM. On the mechanism of ligand-assisted, copper-catalyzed benzylic amination by chloramine-T Organometallics. 29: 3404-3412. DOI: 10.1021/Om100427S  0.779
2010 Barman DN, Nicholas KM. Ligand-assisted, copper-catalyzed enantioselective benzylic amination Tetrahedron Letters. 51: 1815-1818. DOI: 10.1016/J.Tetlet.2010.01.118  0.748
2010 GANESH P, NICHOLAS KM. ChemInform Abstract: Reactions of Cobalt-Complexed Acetylenic Aldehydes with Chiral (γ -Alkoxyallyl)boranes: Enantioselective Synthesis of 3,4-Dioxy 1,5- Enynes and Stereoselective Entry to Polyfunctional Building Blocks. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199730035  0.321
2010 SRIVASTAVA A, MA Y, PANKAYATSELVAN R, DINGES W, NICHOLAS KM. ChemInform Abstract: Molybdenum-Catalyzed Allylic Amination. Cheminform. 23: no-no. DOI: 10.1002/chin.199243139  0.377
2009 Penoni A, Palmisano G, Zhao YL, Houk KN, Volkman J, Nicholas KM. On the mechanism of nitrosoarene-alkyne cycloaddition. Journal of the American Chemical Society. 131: 653-61. PMID 19093864 DOI: 10.1021/Ja806715U  0.616
2009 Houghton EA, Nicholas KM. In vitro reactive oxygen species production by histatins and copper(I,II). Journal of Biological Inorganic Chemistry : Jbic : a Publication of the Society of Biological Inorganic Chemistry. 14: 243-51. PMID 18975018 DOI: 10.1007/S00775-008-0444-X  0.757
2009 Lamar AA, Nicholas KM. Direct synthesis of 3-arylindoles via annulation of aryl hydroxylamines with alkynes Tetrahedron. 65: 3829-3833. DOI: 10.1016/J.Tet.2009.03.004  0.763
2008 Kalita B, Lamar AA, Nicholas KM. Hydrous zinc halide-catalyzed aminosulfonation of hydrocarbons. Chemical Communications (Cambridge, England). 4291-3. PMID 18802547 DOI: 10.1039/B805783D  0.788
2008 Lin Y, Volkman J, Nicholas KM, Yamamoto T, Eguchi T, Nimmo SL, West AH, Cook PF. Chemical mechanism of homoisocitrate dehydrogenase from Saccharomyces cerevisiae. Biochemistry. 47: 4169-80. PMID 18321070 DOI: 10.1021/Bi702361J  0.559
2007 Srivastava RS, Tarver NR, Nicholas KM. Mechanistic studies of copper(I)-catalyzed allylic amination. Journal of the American Chemical Society. 129: 15250-8. PMID 18004850 DOI: 10.1021/ja0751072  0.412
2007 Matsumoto M, Nicholas KM. Synthesis of cyclic oligomers from histidine-derived building blocks using dynamic combinatorial chemistry. The Journal of Organic Chemistry. 72: 9308-13. PMID 17967035 DOI: 10.1021/jo701832m  0.524
2007 Zhou L, Powell D, Nicholas KM. Tripodal bis(imidazole) thioether copper(I) complexes: mimics of the Cu(M) site of copper hydroxylase enzymes. Inorganic Chemistry. 46: 7789-99. PMID 17713902 DOI: 10.1021/ic700447k  0.332
2007 Zhou L, Powell D, Nicholas KM. Copper(I) complexes of tripodal tris(imidazolyl) ligands: potential mimics of the Cu(A) site of hydroxylase enzymes. Inorganic Chemistry. 46: 2316-21. PMID 17295473 DOI: 10.1021/ic061985+  0.339
2007 Lin Y, Alguindigue SS, Volkman J, Nicholas KM, West AH, Cook PF. Complete kinetic mechanism of homoisocitrate dehydrogenase from Saccharomyces cerevisiae. Biochemistry. 46: 890-8. PMID 17223711 DOI: 10.1021/Bi062067Q  0.509
2006 Zhou L, Powell D, Nicholas KM. Tripodal bis(imidazole) thioether copper(I) complexes: mimics of the Cu(B) site of hydroxylase enzymes. Inorganic Chemistry. 45: 3840-2. PMID 16676937 DOI: 10.1021/ic052121b  0.315
2006 Penoni A, Palmisano G, Broggini G, Kadowaki A, Nicholas KM. Efficient synthesis of N-methoxyindoles via alkylative cycloaddition of nitrosoarenes with alkynes. The Journal of Organic Chemistry. 71: 823-5. PMID 16409003 DOI: 10.1021/jo051609r  0.337
2005 Srivastava RS, Khan MA, Nicholas KM. Nitrosoarene-CuI complexes are intermediates in copper-catalyzed allylic amination. Journal of the American Chemical Society. 127: 7278-9. PMID 15898753 DOI: 10.1021/ja044093m  0.382
2005 Srivastava RS, Nicholas KM. Kinetics of the allylic amination of olefins by nitroarenes catalyzed by [CpFe(CO) 2] 2 Organometallics. 24: 1563-1568. DOI: 10.1021/om049336y  0.334
2005 Kalita B, Nicholas KM. Copper-catalyzed allylic hydroxyamination and amination of alkenes with Boc-hydroxylamine Tetrahedron Letters. 46: 1451-1453. DOI: 10.1016/j.tetlet.2005.01.024  0.409
2005 Kalita B, Nicholas KM. Copper-Catalyzed Allylic Hydroxyamination and Amination of Alkenes with Boc-Hydroxylamine. Cheminform. 36. DOI: 10.1002/chin.200525058  0.409
2004 Volkman J, Nicholas KM. Efficient synthesis of tris(4-imidazolyl)methanol derivatives. Organic Letters. 6: 4301-2. PMID 15524468 DOI: 10.1021/Ol048214Z  0.548
2004 O'Dell DK, Nicholas KM. Synthesis of 1H-indazoles by reductive cyclization of o-nitro-ketoximes Heterocycles. 63: 373-382. DOI: 10.3987/Com-03-9926  0.778
2004 Kalita B, Nicholas KM. Synthesis of α-substituted iminodiacetate ligands: α-hexadienyl derivatives for the selection of lipoxygenase mimics Tetrahedron. 60: 10771-10778. DOI: 10.1016/j.tet.2004.08.029  0.301
2003 O'Dell DK, Nicholas KM. Synthesis of 3-substituted quinolines via transition-metal-catalyzed reductive cyclization of o-nitro Baylis-Hillman acetates. The Journal of Organic Chemistry. 68: 6427-30. PMID 12895081 DOI: 10.1021/jo034447c  0.773
2003 O'Dell DK, Nicholas KM. Unexpected products from the Fp2-catalyzed reductive cyclization of nitroaromatics bearing pendant unsaturation Tetrahedron. 59: 747-754. DOI: 10.1016/S0040-4020(02)01627-7  0.758
2003 Hogan GA, Gallo AA, Nicholas KM, Srivastava RS. Cu(I)-Catalyzed Allylic Amination of Olefins. Cheminform. 34. DOI: 10.1002/chin.200312049  0.349
2002 Nicholas KM, Wentworth P, Harwig CW, Wentworth AD, Shafton A, Janda KD. A cofactor approach to copper-dependent catalytic antibodies. Proceedings of the National Academy of Sciences of the United States of America. 99: 2648-53. PMID 11880619 DOI: 10.1073/Pnas.052001099  0.341
2002 Penoni A, Volkmann J, Nicholas KM. Regioselective synthesis of indoles via reductive annulation of nitrosoaromatics with alkynes. Organic Letters. 4: 699-701. PMID 11869105  0.333
2002 Hogan GA, Gallo AA, Nicholas KM, Srivastava RS. Cu(I)-catalyzed allylic amination of olefins Tetrahedron Letters. 43: 9505-9508. DOI: 10.1016/S0040-4039(02)02441-3  0.43
2001 Arakawa H, Aresta M, Armor JN, Barteau MA, Beckman EJ, Bell AT, Bercaw JE, Creutz C, Dinjus E, Dixon DA, Domen K, DuBois DL, Eckert J, Fujita E, Gibson DH, ... ... Nicholas KM, et al. Catalysis research of relevance to carbon management: progress, challenges, and opportunities. Chemical Reviews. 101: 953-96. PMID 11709862 DOI: 10.1021/Cr000018S  0.588
2000 Franks RJ, Nicholas KM. Palladium-catalyzed carboxylative coupling of allylstannanes and allyl halides Organometallics. 19: 1458-1460. DOI: 10.1021/om0000966  0.777
1998 Srivastava RS, Nicholas KM. Iron-catalyzed allylic amination by nitroorganics Chemical Communications. 2705-2706.  0.319
1997 Ganesh P, Nicholas KM. Reactions of Cobalt-Complexed Acetylenic Aldehydes with Chiral (γ-Alkoxyallyl)boranes:  Enantioselective Synthesis of 3,4-Dioxy 1,5-Enynes and Stereoselective Entry to Polyfunctional Building Blocks The Journal of Organic Chemistry. 62: 1737-1747. DOI: 10.1021/jo9619387  0.312
1997 Srivastava RS, Nicholas KM. On the mechanism of allylic amination catalyzed by iron salts Journal of the American Chemical Society. 119: 3302-3310. DOI: 10.1021/ja964006t  0.305
1997 Shi M, Nicholas KM. Palladium-catalyzed carboxylation of allyl stannanes [12] Journal of the American Chemical Society. 119: 5057-5058. DOI: 10.1021/ja9639832  0.386
1996 Srivastava RS, Nicholas KM. Molybdenum-catalysed allylic animation of alkenes by arylamine-ButOOH Chemical Communications. 2335-2336.  0.328
1993 Ganesh P, Nicholas KM. Reactions of cobalt-complexed acetylenic aldehydes with chiral (γ-alkoxyallyl)boranes: Enantioselective synthesis of 3,4-dioxy 1,5-enynes Journal of Organic Chemistry. 58: 5587-5588.  0.327
1991 Li Z, Nicholas KM. Approaches to selective isoprenologation via reactions of (η3-allyl)Fe(CO)+4 with allyl nucleophiles Journal of Organometallic Chemistry. 402: 105-112. DOI: 10.1016/0022-328X(91)80086-Y  0.312
1990 Pankayatselvan R, Nicholas KM. Regioselectivity of nucleophilic additions to substituted (η4-diene)Co(CO)3BF4 complexes Journal of Organometallic Chemistry. 384: 361-380. DOI: 10.1016/0022-328X(90)87128-Z  0.313
1990 Montaña Pedrero AM, Nicholas KM. 1H and13C NMR determination of the relative stereochemistry of the diastereomers resulting from the reaction of sily enol ethers with the 1-ethoxy-1-propargylium dicobalt hexacarbonyl cation Magnetic Resonance in Chemistry. 28: 486-495. DOI: 10.1002/mrc.1260280604  0.348
1984 Saha M, Nicholas KM. Regio- and stereochemistry of acid-catalyzed opening of (1,2-epoxyalkyne)dicobalt hexacarbonyls Journal of Organic Chemistry. 49: 417-422.  0.364
1983 Padmanabhan S, Nicholas KM. Synthesis of skipped (1,4) diynes via coupling of (propargyl acetate) dicobalt hexacarbonyl complexes with alkynyl alanes Tetrahedron Letters. 24: 2239-2242. DOI: 10.1016/S0040-4039(00)81893-6  0.318
1975 Nicholas KM, Rosan AM. The reaction of nucleophiles with [dicarbonyl(h5-cyclopentadienyl)(h2-acenaphthylene)(iron)]+[tetrafluoroborate]- Journal of Organometallic Chemistry. 84: 351-356. DOI: 10.1016/S0022-328X(00)91400-1  0.33
1972 Nicholas KM, Pettit R. On the stability of α-(alkynyl)dicobalt hexacarbonyl carbonium ions Journal of Organometallic Chemistry. 44. DOI: 10.1016/0022-328X(72)80037-8  0.468
1971 Nicholas K, Bray LS, Davis RE, Pettit R. Tetracarbonyldi-μ-2,2,5,5-tetramethylhex-3-yne-di-iron. A novel complex containing an iron-iron double bond Journal of the Chemical Society D: Chemical Communications. 608. DOI: 10.1039/C29710000608  0.537
1971 Nicholas KM, Pettit R. An alkyne protecting group Tetrahedron Letters. 12: 3475-3478. DOI: 10.1016/S0040-4039(01)97209-0  0.488
1971 NICHOLAS K, BRAY LS, DAVIS RE, PETTIT R. ChemInform Abstract: TETRACARBONYL-DI-MY-2,2,5,5-TETRAMETHYLHEX-3-IN-DI-EISEN, EIN NEUER KOMPLEX MIT EINER EISEN-EISEN-DOPPELBINDUNG Chemischer Informationsdienst. Organische Chemie. 2: no-no. DOI: 10.1002/Chin.197137097  0.522
1970 Amiet G, Nicholas K, Pettit R. Mercuration of cyclobutadienyliron tricarbonyl Journal of the Chemical Society D: Chemical Communications. 161. DOI: 10.1039/C29700000161  0.491
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