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Abbolito, Carmela, Iavarone, Carlo, Illuminati, Gabriello, Stegel, Franco, Vazzoler, Augusto (1969) Nucleophilic heteroaromatic substitution. XXXII. Meisenheimer-type compounds from heteroaromatic substrates. The reaction of methoxide ion with 3,5-dinitro-2-methoxypyridine in methanol and dimethyl sulfoxide-methanol mixtures. Journal Of The American Chemical Society, 91 (24) 6746-6748 doi:10.1021/ja01052a035

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Reference TypeJournal (article/letter/editorial)
TitleNucleophilic heteroaromatic substitution. XXXII. Meisenheimer-type compounds from heteroaromatic substrates. The reaction of methoxide ion with 3,5-dinitro-2-methoxypyridine in methanol and dimethyl sulfoxide-methanol mixtures
JournalJournal Of The American Chemical Society
AuthorsAbbolito, CarmelaAuthor
Iavarone, CarloAuthor
Illuminati, GabrielloAuthor
Stegel, FrancoAuthor
Vazzoler, AugustoAuthor
Year1969 (November)Volume91
Issue24
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/ja01052a035Search in ResearchGate
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Mindat Ref. ID1303513Long-form Identifiermindat:1:5:1303513:4
GUID0
Full ReferenceAbbolito, Carmela, Iavarone, Carlo, Illuminati, Gabriello, Stegel, Franco, Vazzoler, Augusto (1969) Nucleophilic heteroaromatic substitution. XXXII. Meisenheimer-type compounds from heteroaromatic substrates. The reaction of methoxide ion with 3,5-dinitro-2-methoxypyridine in methanol and dimethyl sulfoxide-methanol mixtures. Journal Of The American Chemical Society, 91 (24) 6746-6748 doi:10.1021/ja01052a035
Plain TextAbbolito, Carmela, Iavarone, Carlo, Illuminati, Gabriello, Stegel, Franco, Vazzoler, Augusto (1969) Nucleophilic heteroaromatic substitution. XXXII. Meisenheimer-type compounds from heteroaromatic substrates. The reaction of methoxide ion with 3,5-dinitro-2-methoxypyridine in methanol and dimethyl sulfoxide-methanol mixtures. Journal Of The American Chemical Society, 91 (24) 6746-6748 doi:10.1021/ja01052a035
In(1969, November) Journal Of The American Chemical Society Vol. 91 (24) American Chemical Society (ACS)

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Bemporad, Paola, Illuminati, Gabriello, Stegel, Franco (1969) Nucleophilic heteroaromatic substitution. XXXI. Meisenheimer-type compounds from heteroaromatic substrates. The reaction of methoxide ion with 3,5-dinitro-4-methoxypyridine in methanol solution. Journal Of The American Chemical Society, 91 (24) 6742-6745 doi:10.1021/ja01052a034
ABBOLITO, CARMELA, IAVARONE, CARLO, ILLUMINATI, GABRIELLO, STEGEL, FRANCO, VAZZOLER, AUGUSTO (1970) ChemInform Abstract: NUCLEOPHILE HETEROAROMATISCHE SUBSTITUTION 32. MITT. VERBINDUNGEN VOM MEISENHEIMER-TYP AUS HETEROAROMATEN, RK. DES METHOXIDIONS MIT 3,5-DINITRO-2-METHOXY-PYRIDIN IN METHANOL UND DMSO-METHANOL-GEMISCHEN. Chemischer Informationsdienst. Organische Chemie, 1. doi:10.1002/chin.197009094
DE SANTIS, FRANCO, STEGEL, FRANCO (1974) ChemInform Abstract: MEISENHEIMER-TYPE ADDUCTS FROM HETEROAROMATIC SUBSTRATES, THE REACTION OF METHOXIDE ION WITH 2-METHOXY-3-NITRO- AND 3-METHOXY-2-NITROBENZOTHIOPHENE. Chemischer Informationsdienst, 5 (14) doi:10.1002/chin.197414157
Illuminati, Gabriello., Linda, Paolo., Marino, Gianlorenzo. (1967) Nucleophilic heteroaromatic substitution. XXVIII. Kinetics and mechanism of the reaction of p-toluenethiol with chloroquinolines in methanol solution. Journal Of The American Chemical Society, 89 (14) 3521-3524 doi:10.1021/ja00990a031
Illuminati, Gabriello, La Torre, Francesco, Liggieri, Giancarlo, Sleiter, Giancarlo, Stegel, Franco (1975) Nucleophilic heteroaromatic substitutions. XXXVIII. Evidence for a cyclic mechanism in the reaction of 2-phenoxy-1,3,5-triazine with piperidine in isooctane. Journal Of The American Chemical Society, 97 (7) 1851-1855 doi:10.1021/ja00840a042
Genel, Flavia., Illuminati, Gabriello., Marino, Gianlorenzo. (1967) Nucleophilic heteroaromatic substitution. XXVI. Piperidino dechlorination in chloroquinoline series. Sovent effects on reaction selectivity. Journal Of The American Chemical Society, 89 (14) 3516-3518 doi:10.1021/ja00990a029
ILLUMINATI, GABRIELLO, LA TORRE, FRANCESCO, LIGGIERI, GIANCARLO, SLEITER, GIANCARLO, STEGEL, FRANCO (1975) ChemInform Abstract: NUCLEOPHILIC HETEROAROMATIC SUBSTITUTIONS PART 38, EVIDENCE FOR A CYCLIC MECHANISM IN THE REACTION OF 2-PHENOXY-1,3,5-TRIAZINE WITH PIPERIDINE IN ISOOCTANE. Chemischer Informationsdienst, 6 (25) doi:10.1002/chin.197525101
BEMPORAD, PAOLA, ILLUMINATI, GABRIELLO, STEGEL, FRANCO (1970) ChemInform Abstract: NUCLEOPHILE HETEROAROMATISCHE SUBSTITUTION 31. MITT. VERBINDUNGEN VOM MEISENHEIMER-TYP AUS HETEROAROMATEN, RK. DES METHOXIDIONS MIT 3,5-DINITRO-4-METHOXY-PYRIDIN IN METHANOLISCHER LOESUNG. Chemischer Informationsdienst. Organische Chemie, 1. doi:10.1002/chin.197009093
Calligaris, Mario., Illuminati, Gabriello., Marino, Gianlorenzo. (1967) Nucleophilic heteroaromatic substitution. XXVII. Piperidino dechlorination and methoxy dechlorination of 6- and 8-alkyl-4-chloroquinolines. Steric hindrance to specific solvation. Journal Of The American Chemical Society, 89 (14) 3518-3521 doi:10.1021/ja00990a030
Zoltewicz, John A., Oestreich, Terence M. (1973) Heteroaromatic nucleophilic substitution. Inducing a change from an ionic to a radical-chain mechanism with methoxide ion. Journal Of The American Chemical Society, 95 (20) 6863-6864 doi:10.1021/ja00801a072
Baciocchi, Enrico., Illuminati, Gabriello., Sleiter, Giancarlo., Stegel, Franco. (1967) The Kinetic Hydrogen Isotope Effects in the Bromination of Some Polyalkylbenzene Systems. Journal Of The American Chemical Society, 89 (1) 125-129 doi:10.1021/ja00977a024
 
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