Year |
Citation |
Score |
2015 |
Prakash GK, Papp A, Munoz SB, May N, Jones JP, Haiges R, Esteves PM, Mathew T. Lewis Acid Catalyzed Condensation-Cyclization Cascade: Direct Synthesis of Di/Trifluoromethyl-1,2,3,4-tetrahydroquinazolines. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26038834 DOI: 10.1002/Chem.201500744 |
0.693 |
|
2013 |
Firme CL, da Costa TF, da Penha ET, Esteves PM. Electronic structures of bisnoradamantenyl and bisnoradamantanyl dications and related species. Journal of Molecular Modeling. 19: 2485-97. PMID 23446438 DOI: 10.1007/s00894-013-1785-0 |
0.732 |
|
2010 |
Louis B, Pereira MM, Santos FM, Esteves PM, Sommer J. Alkane activation over acidic zeolites: the first step. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 573-6. PMID 19918812 DOI: 10.1002/chem.200901737 |
0.679 |
|
2009 |
Firme CL, Antunes OA, Esteves PM, Corrêa RJ. Derivatives of spiropentadiene dication: new species with planar tetracoordinate carbon (ptC) atom. The Journal of Physical Chemistry. A. 113: 3171-6. PMID 19278214 DOI: 10.1021/jp807400j |
0.718 |
|
2009 |
de Almeida LS, Esteves PM, de Mattos MCS. Superelectrophilic bromination of deactivated aromatic rings with tribromoisocyanuric acid-an experimental and DFT study Tetrahedron Letters. 50: 3001-3004. DOI: 10.1016/j.tetlet.2009.02.010 |
0.314 |
|
2008 |
Firme CL, Antunes OA, Esteves PM. Electronic nature of carbonium ions and their silicon analogues. The Journal of Physical Chemistry. A. 112: 3165-71. PMID 18311954 DOI: 10.1021/jp710606n |
0.718 |
|
2008 |
Firme CL, Barreiro NB, Esteves PM, Corrêa RJ. Understanding the planar tetracoordinate carbon atom: spiropentadiene dication. The Journal of Physical Chemistry. A. 112: 686-92. PMID 18179183 DOI: 10.1021/jp074895e |
0.702 |
|
2007 |
Firme CL, Antunes OA, Esteves PM. Electronic nature of planar cyclobutenyl dication derivatives. The Journal of Physical Chemistry. A. 111: 11904-7. PMID 17948974 DOI: 10.1021/jp075869j |
0.72 |
|
2006 |
de Souza RO, Esteves PM, Laali KK. Allenediazonium ions and their protonation chemistry: a DFT study. Organic & Biomolecular Chemistry. 4: 4444-52. PMID 17268637 DOI: 10.1039/b611304b |
0.319 |
|
2006 |
Fleming FP, Barbosa AG, Esteves PM. Nature of the chemical bond in protonated methane. The Journal of Physical Chemistry. A. 110: 11903-5. PMID 17064177 DOI: 10.1021/jp0654260 |
0.323 |
|
2006 |
Prakash GK, Mathew T, Marinez ER, Esteves PM, Rasul G, Olah GA. BF3.2CF3CH2OH (BF3.2TFE), an efficient superacidic catalyst for some organic synthetic transformations. The Journal of Organic Chemistry. 71: 3952-8. PMID 16674072 DOI: 10.1021/Jo0604181 |
0.457 |
|
2004 |
Prakash GK, Mathew T, Hoole D, Esteves PM, Wang Q, Rasul G, Olah GA. N-halosuccinimide/BF3-H2O, efficient electrophilic halogenating systems for aromatics. Journal of the American Chemical Society. 126: 15770-6. PMID 15571400 DOI: 10.1021/Ja0465247 |
0.407 |
|
2004 |
Olah GA, Mathew T, Goeppert A, Rasul G, Prakash GK, Esteves PM. Carbocationic rearrangement of pivaloyl cation and protonated pivalaldehyde in superacid medium: a novel solution equivalent of the McLafferty rearrangement. Journal of the American Society For Mass Spectrometry. 15: 959-65. PMID 15234354 DOI: 10.1016/J.Jasms.2004.05.002 |
0.47 |
|
2004 |
Olah GA, Mathew T, Goeppert A, Rasul G, Prakash GKS, Esteves PM. Carbocationic rearrangement of pivaloyl cation and protonated pivalaldehyde in superacid medium: A novel solution equivalent of the McLafferty rearrangement Journal of the American Society For Mass Spectrometry. 15: 959-965. DOI: 10.1016/j.jasms.2004.05.002 |
0.314 |
|
2002 |
Olah GA, Török B, Joschek JP, Bucsi I, Esteves PM, Rasul G, Surya Prakash GK. Efficient chemoselective carboxylation of aromatics to arylcarboxylic acids with a superelectrophilically activated carbon dioxide-Al(2)Cl(6)/Al system. Journal of the American Chemical Society. 124: 11379-91. PMID 12236753 DOI: 10.1021/Ja020787O |
0.418 |
|
2001 |
Olah GA, Mathew T, Marinez ER, Esteves PM, Etzkorn M, Rasul G, Surya Prakash GK. Acid-catalyzed isomerization of pivalaldehyde to methyl isopropyl ketone via a reactive protosolvated carboxonium ion intermediate Journal of the American Chemical Society. 123: 11556-11561. PMID 11716708 DOI: 10.1021/Ja011253A |
0.669 |
|
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