G. Marino

发表

Effect of physical parameters on the main phase transition of supported lipid bilayers.

A. Alessandrini, P. Facci, H. Seeger, 2009, Biophysical journal.

A comparative study of the aromatic character of furan, thiophen, selenophen, and tellurophen

F. Fringuelli, G. Marino, A. Taticchi, 1974 .

Meta-substituent effects on the kinetics of methoxydechlorination of some 2- and 4-chloroquinolines

G. Marino, G. Illuminati, M. Belli, 1963 .

Photoelectron spectra of the α-substituted derivatives of furan, thiophen, selenophen, and tellurophen. A comparative study of the molecular orbital energies

G. Distefano, F. Fringuelli, G. Marino, 1976 .

A comparison of sensitivities to substituent effects of five-membered heteroaromatic rings in gas phase ionization

P. Linda, G. Marino, S. Pignataro, 1971 .

Linear free energy relationships for electrophilic substitutions at α- and β-positions of thiophen

S. Clementi, P. Linda, G. Marino, 1970 .

The “extended selectivity treatment” for electrophilic substitutions at the position of the furan ring

S. Clementi, P. Linda, G. Marino, 1970 .

Electrophilic substitution in five-membered heterocyclic systems. Part VI. Kinetics of the bromination of the 2-methoxycarbonyl derivatives of furan, thiophen, and pyrrole in acetic acid solution

P. Linda, G. Marino, 1968 .

A quantitative study of the uncatalysed halogenation of thiophene in acetic acid solution

G. Marino, 1965 .

The mechanism of the Vilsmeier–Haack reaction. Part III. Structural and solvent effects

G. Savelli, P. Linda, G. Marino, 1974 .

Relative reactivities and activation parameters for the Vilsmeier–Haack formylation of five-membered heteroaromatic compounds containing the Group VI elements

S. Clementi, F. Fringuelli, G. Savelli, 1973 .

The mechanism of the Vilsmeier–Haack reaction. Part II. A kinetic study of the formylation of thiophen derivatives with dimethylformamide and phosphorus oxychloride or carbonyl chloride in 1,2-dichloroethane

G. Savelli, P. Linda, G. Marino, 1972 .

Electronic transmission of substituent effects through the tellurophen ring

F. Fringuelli, G. Marino, A. Taticchi, 1972 .

The aromatic reactivity of tellurophen

F. Fringuelli, G. Savelli, G. Marino, 1971 .

Substituent effects in the trifluoroacetylation of substituted thiophens, furans, and pyrroles

S. Clementi, G. Marino, 1970 .

Kinetics and mechanism of the vilsmeier formylation of thiophen derivatives

P. Linda, G. Marino, S. Santini, 1970 .

Relative reactivities of thiophen, furan, and pyrrole rings in electrophilic substitutions: trifluoroacetylation

S. Clementi, G. Marino, F. Genel, 1967 .

Relative reactivities of thiophen, furan, and pyrrole rings in electrophilic substitutions: bromination of the 2-methoxycarbonyl derivatives

P. Linda, G. Marino, 1967 .

Relative reactivities of some furan and thiophene derivatives in the iodine- and tin tetrachloride-catalysed acetylations with acetic anhydride in dichloroethane☆

P. Linda, G. Marino, 1967 .

Nucleophilic heteroaromatic substitution. XXVIII. Kinetics and mechanism of the reaction of p-toluenethiol with chloroquinolines in methanol solution

P. Linda, G. Marino, G. Illuminati, 1967 .

Relative Rates and Isomer Distributions in the Acetylation of the Methylbenzenes by Acetyl Chloride-Aluminum Chloride in Ethylene Dichloride Solution1

H. Brown, G. Marino, 1959 .

Kinetics and mechanism of N-substitution of indoles and carbazoles in Vilsmeier–Haack acetylation

S. Clementi, A. Cipiciani, G. Savelli, 1977 .

The Determination of Reactivities meta and para to Halogens. The Bromination of Some Halopolymethylbenzenes by Bromine in Nitromethane1,2

G. Marino, G. Illuminati, 1956 .

Nucleophilic heteroaromatic substitution—XXIV: Kinetics of piperidinodechlorination of 2- and 6- alkyl-4-chloropyrimidines in ethanol and toluene—evidence for a steric hindrance to solvation of the aza-group☆

P. Linda, G. Marino, M. Calligaris, 1967 .

Nucleophilic heteroaromatic substitution. XXVII. Piperidino dechlorination and methoxy dechlorination of 6- and 8-alkyl-4-chloroquinolines. Steric hindrance to specific solvation

G. Marino, M. Calligaris, G. Illuminati, 1967 .

The mechanism of trifluoroacetylation of indoles

S. Clementi, A. Cipiciani, G. Savelli, 1982 .

Competitive ipso-attack at C-3 and N-substitution in the trifluoroacetylation of 2,3-dimethylindole

S. Clementi, A. Cipiciani, G. Savelli, 1980 .

Reactivity of indoles in electrophilic substitution

S. Clementi, P. Linda, G. Marino, 1972 .

Ionization energies of selenophen, tellurophen and some of their derivatives

G. Innorta, G. Distefano, F. Fringuelli, 1973 .

Tellurophene and Related Compounds

F. Fringuelli, G. Marino, A. Taticchi, 1977 .

Rate Data and Isomer Distributions in the Acetylation and Benzoylation of Ethyl-, Isopropyl- and t-Butylbenzene. Partial Rate Factors for the Acylation Reaction1

H. Brown, G. Marino, 1959 .

The Relative Rate and Isomer Distribution in the Acetylation of Benzene and Toluene in Ethylene Dichloride under the Influence of Aluminum Chloride1,2

H. Brown, L. Stock, G. Marino, 1959 .

Piperidino dechlorination of chloroquinolines. Solvent effects on the reaction kinetics

G. Marino, G. Sleiter, G. Illuminati, 1967 .

Kinetics of the Reaction of Benzoyl Halides with Toluene in Non-polar Solvents under the Influence of Aluminum Halides1,2

F. R. Jensen, H. Brown, G. Marino, 1959 .

Nucleophilic heteroaromatic substitution. XXVI. Piperidino dechlorination in chloroquinoline series. Sovent effects on reaction selectivity

G. Marino, G. Illuminati, F. Genel, 1967 .

Electronic Transmission through Condensed-ring Systems. II. The Kinetics of Methoxydechlorination of Some 6- and 7-Substituted 1-Aza-4-chloronaphthalenes1,2

G. Marino, G. Illuminati, 1958 .

Electrophilic substitutions in five-membered heterocyclic systems. Part VII. The reactivity of selenophen towards electrophiles. A comparison with thiophen

P. Linda, G. Marino, 1970 .

A comparative study of the aromatic character of furan, thiophen, selenophen, and tellurophen

F. Fringuelli, G. Marino, A. Taticchi, 1974 .

Heteroaromatic rings as substituents. Part I. Evaluation of σ- and σ–-constants of 2- and 3-thienyl groups

F. Fringuelli, G. Marino, A. Taticchi, 1970 .

Substitution in Polymethylbenzenes. III. A New Route to Isodurene Derivatives1

G. Marino, G. Illuminati, 1953 .

Heteroaromatic rings as substituents. Part II. Evaluation of the electrophilic substituent constants for 2- and 3-thienyl groups from the solvolysis of 2-chloro-2-(thienylphenyl)propanes in 90% aqueous acetone

F. Fringuelli, G. Marino, A. Taticchi, 1971 .