Pascal and Francis Bibliographic Databases

Help

Search results

Your search

au.\*:("INESI A")

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 26

  • Page / 2
Export

Selection :

  • and

MESO- AND DE-DIETHYL 2,3-DIPHENYLSUCCINATE FROM THE ELECTROCHEMICAL REDUCTION OF ETHYL ALPHA -BROMOPHENYLACETATERAMPAZZO L; INESI A.1980; J. ELECTROCHEM. SOC.; ISSN 0013-4651; USA; DA. 1980; VOL. 127; NO 11; PP. 2388-2391; BIBL. 21 REF.Article

REDUCTION OF ALIPHATIC BROMOESTERS. II: ELECTROCHEMICALLY GENERATED CARBANIONS AND DERIVATIVE CARBANIONS-THEIR REACTIVITY ON ELECTROPHILIC SUBSTRATESINESI A; ZEULI E.1983; JOURNAL OF ELECTROANALYTICAL CHEMISTRY AND INTERFACIAL ELECTROCHEMISTRY; ISSN 0022-0728; CHE; DA. 1983; VOL. 149; NO 1-2; PP. 167-178; BIBL. 18 REF.Article

ELECTROCHEMICAL REDUCTION OF TRANS- AND CIS-ALPHA , ALPHA '-DIFLUOROSTILBENE AT A MERCURY CATHODEINESI A; RAMPAZZO L.1975; ANN. CHIM.; ITAL.; DA. 1975; VOL. 65; NO 5-6; PP. 279-286; ABS. ITAL.; BIBL. 22 REF.Article

STEREOSELECTIVE REDUCTION OF MESO- AND DL-1,2-DIBROMO-1,2-DIPHENYLETHANE AT THE MERCURY ELECTRODEINESI A; RAMPAZZO L.1974; J. ELECTROANAL. CHEM. INTERFACIAL ELECTROCHEM.; NETHERL.; DA. 1974; VOL. 54; NO 2; PP. 289-295; BIBL. 25 REF.Article

BENZOCYCLOBUTADIENE DIMER FROM THE ELECTROCHEMICAL REDUCTION OF ALPHA ,ALPHA ,ALPHA ',ALPHA '-TETRABROMO-O-XYLENE.RAMPAZZO L; INESI A; MARINI BETTOLO R et al.1977; J. ELECTROANAL. CHEM. INTERFACIAL ELECTROCHEM.; NETHERL.; DA. 1977; VOL. 83; NO 2; PP. 341-346; BIBL. 21 REF.Article

ELECTROCATALYSIS AND REDUCTION OF FLUORINATED ESTERS: THE ROLE OF SOME AROMATIC HYDROCARBONSINESI A; RAMPAZZO L; ZEPPA A et al.1978; ANN. CHIM.; ITA; DA. 1978; VOL. 68; NO 9-10; PP. 771-782; ABS. ITA; BIBL. 15 REF.Article

DIRECT AND INDIRECT REDUCTION OF ETHYL BETA -BROMOPROPIONATE AND ETHYL GAMMA -BROMOVALERATE IN DMF SOLUTIONSINESI A; ZEPPA A; ZEULI E et al.1981; J. ELECTROANAL. CHEM. INTERFACIAL ELECTROCHEM.; ISSN 0022-0728; CHE; DA. 1981; VOL. 126; NO 1-3; PP. 175-187; BIBL. 15 REF.Article

Reactivity of 2-chloro- and 2-(tosyloxy)cyclohexanones towards anions electrogenerated at carbonium and nitrogen atoms. Electrochemically induced Favorskii rearrangementDE ANGELIS, F; FEROCI, M; INESI, A et al.Bulletin de la Société chimique de France. 1993, Vol 130, Num 5, pp 712-719, issn 0037-8968Article

Electrochemical reduction of bromomethyl phenyl ketoneCARELLI, I; CURULLI, A; INESI, A et al.Journal of chemical research. Synopses (Print). 1988, Num 5, pp 154-155, issn 0308-2342Article

The reactivity of the electrogenerated cyanoisopropyl anion (CMe2CN) versus SN2 and acid-base reactionsCARELLI, I; CURULLI, A; INESI, A et al.Journal of chemical research. Synopses (Print). 1985, Num 12, pp 390-391, issn 0308-2342Article

Electrochemical studies on β-lactams. I: Electroreduction of 3-halogeno-β-lactamsCASADEI, M. A; MORACCI, F. M; INESI, A et al.Perkin transactions. 2. 1986, Num 3, pp 419-423, issn 0300-9580Article

Heterogeneous electrode-assisted ionization in the reduction of α,β-dibromoestersGIOMINI, C; INESI, A; ZEULI, E et al.Electrochimica acta. 1984, Vol 29, Num 8, pp 1107-1109, issn 0013-4686Article

Electrochemical synthesis of 5,6,11,12-tetrahydro-5,6,11,12-tetrakis(ethoxycarbonyl) dibenzo [a,e] cyclo-octeneDE LUCA, C; INESI, A; RAMPAZZO, L et al.Perkin transactions. 2. 1983, Num 12, pp 1821-1825, issn 0300-9580Article

Small-ring synthesis induced by the electrogenerated superoxide anionCARELLI, I; CURULLI, A; INESI, A et al.Journal of chemical research. Synopses (Print). 1989, Num 11, pp 338-339, issn 0308-2342Article

Electrochemical alkylation of cyclic and linear ketonesCURULLI, A; INESI, A; ZEULI, E et al.Electrochimica acta. 1987, Vol 32, Num 7, pp 1117-1118, issn 0013-4686Article

Reactivity of the electrogenerated superoxide ion. II, Favorskii rearrangementsCARELLI, I; CURULLI, A; INESI, A et al.Journal of chemical research. Synopses (Print). 1991, Num 1, pp 10-11, issn 0308-2342Article

Electrochemical synthesis of diethyl 2,3-bis-p-halogenophenylsuccinates; reduction of α-bromo-p-halogenophenylacetatesDE LUCA, C; INESI, A; RAMPAZZO, L et al.Perkin transactions. 2. 1987, Num 7, pp 847-852, issn 0300-9580Article

Electrogenerated N-heterocyclic carbenes : N-functionalization of benzoxazolonesCHIAROTTO, I; FEROCI, M; ORSINI, M et al.Tetrahedron (Oxford. Print). 2009, Vol 65, Num 18, issn 0040-4020, 3558 3704-3710 [8 p.]Article

Electrochemical studies on β-lactams. IV: Electroacetylation of β-lactamsCASADEI, M. A; INESI, A; MORACCI, F. M et al.Tetrahedron (Oxford. Print). 1989, Vol 45, Num 21, pp 6885-6890, issn 0040-4020Article

Electrochemical reduction of N-(2,2,2-trichloroethyl)acetamidesCASADEI, M. A; MORACCI, F. M; OCCHIALINI, D et al.Perkin transactions. 2. 1987, Num 12, pp 1887-1892, issn 0300-9580Article

Electrochemically promoted C-N bond formation from amines and CO2 in ionic liquid BMIm-BF4 : Synthesis of carbamatesFEROCI, M; ORSINI, M; ROSSI, L et al.Journal of organic chemistry. 2007, Vol 72, Num 1, pp 200-203, issn 0022-3263, 4 p.Article

An electrochemical alternative strategy to the synthesis of β-lactams. Part 2 [1]. C3-C4 bond formationFEROCI, M; ORSINI, M; ROSSI, L et al.Electrochimica acta. 2006, Vol 51, Num 25, pp 5540-5547, issn 0013-4686, 8 p.Article

An electrochemical alternative strategy to the synthesis of β-lactams Part 3 [1]. Room-temperature ionic liquids vs molecular organic solventsSOTGIU, G; CHIAROTTO, I; FEROCI, M et al.Electrochimica acta. 2008, Vol 53, Num 27, pp 7852-7858, issn 0013-4686, 7 p.Article

Electrochemical studies on haloamides. III: Haloacetamides and haloacetohydroxamatesCASADEI, M. A; DI RIENZO, B; INESI, A et al.Journal of the Chemical Society. Perkin transactions. I. 1992, Num 3, pp 375-378, issn 0300-922XArticle

Electrochemical studies on haloamides. IV: Reactivity of halocetamides and haloacetohyroxamates toward electrogenerated diethyl malonate anionCASADEI, M. A; DI RIENZO, B; INESI, A et al.Journal of the Chemical Society. Perkin transactions. I. 1992, Num 3, pp 379-382, issn 0300-922XArticle

  • Page / 2