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 |
|
Show low-probability matches. |