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Bacaloglu, Radu, Bunton, Clifford A., Ortega, Francisco (1989) Interaction of nitroarenes with hydroxide ion. An AM1 molecular orbital treatment. Journal Of The American Chemical Society, 111 (3) 1041-1047 doi:10.1021/ja00185a038

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Reference TypeJournal (article/letter/editorial)
TitleInteraction of nitroarenes with hydroxide ion. An AM1 molecular orbital treatment
JournalJournal Of The American Chemical Society
AuthorsBacaloglu, RaduAuthor
Bunton, Clifford A.Author
Ortega, FranciscoAuthor
Year1989 (February)Volume111
Issue3
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/ja00185a038Search in ResearchGate
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Mindat Ref. ID1437536Long-form Identifiermindat:1:5:1437536:7
GUID0
Full ReferenceBacaloglu, Radu, Bunton, Clifford A., Ortega, Francisco (1989) Interaction of nitroarenes with hydroxide ion. An AM1 molecular orbital treatment. Journal Of The American Chemical Society, 111 (3) 1041-1047 doi:10.1021/ja00185a038
Plain TextBacaloglu, Radu, Bunton, Clifford A., Ortega, Francisco (1989) Interaction of nitroarenes with hydroxide ion. An AM1 molecular orbital treatment. Journal Of The American Chemical Society, 111 (3) 1041-1047 doi:10.1021/ja00185a038
In(1989, February) Journal Of The American Chemical Society Vol. 111 (3) American Chemical Society (ACS)

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Bacaloglu, Radu, Blasko, Andrei, Bunton, Clifford, Dorwin, Ellen, Ortega, Francisco, Zucco, Cesar (1991) Mechanism of reaction of hydroxide ion with dinitrochlorobenzenes. Journal Of The American Chemical Society, 113 (1) 238-246 doi:10.1021/ja00001a034
Bacaloglu, Radu., Bunton, Clifford A., Ortega, Francisco. (1988) Single-electron transfer in aromatic nucleophilic substitution in reaction of 1-substituted 2,4-dinitronaphthalenes with hydroxide ion. Journal Of The American Chemical Society, 110 (11) 3512-3518 doi:10.1021/ja00219a027
Bacaloglu, Radu, Blasko, Andrei, Bunton, Clifford A., Ortega, Francisco (1990) Single-electron transfer in deacylation of ethyl dinitrobenzoates. Journal Of The American Chemical Society, 112 (25) 9336-9344 doi:10.1021/ja00181a040
Bacaloglu, Radu., Bunton, Clifford A., Ortega, Francisco. (1988) Single-electron transfer in aromatic nucleophilic addition and substitution in aqueous media. Journal Of The American Chemical Society, 110 (11) 3503-3512 doi:10.1021/ja00219a026
Bacaloglu, Radu, Blasko, Andrei, Bunton, Clifford A., Ortega, Francisco, Zucco, Cesar (1992) Single-electron transfer in aromatic nucleophilic substitution on dinitrobenzonitriles. Journal Of The American Chemical Society, 114 (20) 7708-7718 doi:10.1021/ja00046a017
Bacaloglu, Radu., Bunton, Clifford A., Cerichelli, Giorgio., Ortega, Francisco. (1988) Proton exchange and NMR line broadening in aromatic nucleophilic addition and substitution. Journal Of The American Chemical Society, 110 (11) 3495-3503 doi:10.1021/ja00219a025
Bacaloglu, Radu, Bunton, Clifford A., Cerichelli, Giorgio, Ortega, Francisco (1989) NMR study of the location of bromide ion and methyl naphthalene-2-sulfonate in cationic micelles: relation to reactivity. The Journal of Physical Chemistry, 93 (4). 1490-1497 doi:10.1021/j100341a060
Bacaloglu, Radu, Bunton, Clifford A., Ortega, Francisco (1989) Micellar enhancements of rates of SN2 reactions of halide ions: the effect of head group size. The Journal of Physical Chemistry, 93 (4). 1497-1502 doi:10.1021/j100341a061
Bacaloglu, Radu., Bunton, Clifford A., Cerichelli, Giorgio., Ortega, Francisco. (1990) Micellar effects upon rates of SN2 reactions of chloride ion. II. Effects of cationic headgroups. The Journal of Physical Chemistry, 94 (12). 5068-5073 doi:10.1021/j100375a057
Bacaloglu, Radu, Bunton, Clifford A., Cerichelli, Giorgio (1987) Intermediates in nucleophilic aromatic substitution. Journal Of The American Chemical Society, 109 (2) 621-623 doi:10.1021/ja00236a072
Bacaloglu, Radu., Blasko, Andrei., Bunton, Clifford A., Cerichelli, Giorgio., Ortega, Francisco. (1990) Micellar effects upon rates of SN2 reactions of chloride ion. I. Effects of variations in the hydrophobic tails. The Journal of Physical Chemistry, 94 (12). 5062-5068 doi:10.1021/j100375a056
 
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