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IPSO- AND TELE-SUBSTITUTION PATHWAYS IN THE REACTIONS OF 1,3-DIMETHYL-2,4-DINITRO- AND 1,3-DIMETHYL-2-NITRO-4-PHENYLSULPHONYL-NAPHTHALENE WITH SODIUM ARENETHIOLATES IN DIMETHYL SULPHOXIDENOVI M; DELL'ERBA C; SANCASSAN F et al.1983; PERKIN TRANSACTIONS 1; ISSN 0300-922X; GBR; DA. 1983; NO 6; PP. 1145-1149; BIBL. 13 REF.Article

A LANTHANIDE INDUCED SHIF (LIS) INVESTIGATION OF THE CONFORMATION OF CYCLOHEXANONES IN SOLUTIONABRAHAM RJ; BOVILL MJ; CHADWICK DJ et al.1980; TETRAHEDRON; GBR; DA. 1980; VOL. 36; NO 2; PP. 279-285; BIBL. 37 REF.Article

AN UNUSUAL NUCLEOPHILIC SUBSTITUTION ON AN AROMATIC SUBSTRATE. REACTION OF 2,5-DIMETHYL-3,4-DINITROTHIOPHEN WITH SODIUM ARENETHIOLATES IN METHANOLNOVI M; SANCASSAN F; GUANTI G et al.1976; J. CHEM. SOC. CHEM. COMMUNIC.; G.B.; DA. 1976; NO 8; PP. 303-304; BIBL. 2 REF.Article

CINE-SUBSTITUTION IN THE THIOPHEN SERIES. MECHANISM OF THE REACTION OF 3,4-DINITROTHIOPHEN WITH SODIUM ARENETHIOLATES IN METHANOLNOVI M; GUANTI G; SANCASSAN F et al.1978; J. CHEM. SOC., PERKIN TRANS., 1; GBR; DA. 1978; NO 10; PP. 1140-1144; BIBL. 14 REF.Article

NORMAL SNAR, TELESUBSTITUTION, AND ELECTRON-TRANSFER PATHWAYS IN THE REACTIONS OF METHYL-SUBSTITUTED O-BIS(PHENYLSULFONYL) BENZENE DERIVATIVES WITH SODIUM ARENETHIOLATES IN DIMETHYL SULFOXIDENOVI M; DELL'ERBA C; GARBARINO G et al.1982; J. ORG. CHEM.; ISSN 0022-3263; USA; DA. 1982; VOL. 47; NO 12; PP. 2292-2298; BIBL. 22 REF.Article

DIRECT LANTHANIDE-INDUCED-SHIFT NMR DETERMINATION OF CONFORMER POPULATIONS IN SUBSTITUTED CYCLOHEXANONESABRAHAM RJ; CHADWICK DJ; GRIFFITHS L et al.1980; J. AMER. CHEM. SOC.; USA; DA. 1980; VOL. 102; NO 15; PP. 5128-5130; BIBL. 12 REF.Article

Conformational analysis. IX: A lanthanide-induced shift (LIS) nuclear magnetic resonance investigation of conformational isomerism and structure in 1- and 2-naphthaldehyde, 9-acetylanthracene, and 9-anthraldehydeABRAHAM, R. J; CHADWICK, D. J; SANCASSAN, F et al.Perkin transactions. 2. 1988, Num 2, pp 169-176, issn 0300-9580Article

Inhaltsstoffe von Cupuliferae. VIII: Ein neues, hoch acyliertes Astragalin aus Quercus ilex L = Constituants des cupulifères. VIII: une nouvelle astragaline, fortement acylée, isolée de Quercus ilex L = Constituents of Cupuliferae. VIII: a novel, highly acylated astragalin from Quercus ilex LROMUSSI, G; SANCASSAN, F; PARODI, B et al.Liebigs Annalen der Chemie. 1984, Num 11, pp 1864-1866, issn 0170-2041Article

Conformational analysis : 18* : lanthanide-induced shift (LIS) investigation of some 2-substituted 1,3-dioxanesABRAHAM, R. J; WALLACE, K; WILKINS, S et al.Magnetic resonance in chemistry. 1992, Vol 30, Num 10, pp 1019-1024, issn 0749-1581Article

Meisenheimer-type adducts from thiophene derivatives. VII, Interdependence of 13C NMR, thermodynamic and kinetic dataDELL'ERBA, C; SANCASSAN, F; NOVI, M et al.Perkin transactions. 2. 1991, Num 10, pp 1631-1636, issn 0300-9580Article

Reaction of ketenes with N,N-disubstituted α-aminomethyleneketones. XIX: Synthesis of N,N-disubstituted 4-amino-3-phenyl-2H-furo[2,3-h]-1-benzopyran-2-ones (4-amino-3-phenylangelicins). Crystal and molecular structure of 3-phenylangelicinMOSTI, L; SCHENONE, P; MENOZZI, G et al.Journal of heterocyclic chemistry. 1988, Vol 25, Num 2, pp 407-413, issn 0022-152XArticle

Meisenheimer-type adducts from thiophene derivatives. II: Kinetic, thermodynamic, and 13C N.m.r. studies of substituent effects in the reaction of sodium methoxide with some 2-methoxy-3-nitro-5-X-thiophenes in methanolCONSIGLIO, G; SPINELLI, D; ARNONE, C et al.Perkin transactions. 2. 1984, Num 2, pp 317-323, issn 0300-9580Article

On the nature of resonance interactions in substituted benzenes. III, A 13C nuclear magnetic resonance study of substituent effects in 4-substituted benzamides and methyl benzoates in dimethyl sulphoxideDELL'ERBA, C; MELE, A; NOVI, M et al.Perkin transactions. 2. 1990, Num 12, pp 2055-2058, issn 0300-9580, 4 p.Article

Basicity (pKBH-) and acidity constants (pKa*) of some 3-×-, 4-×-, and 2,6-dimethyl-4-×-benzoic acidsDE MARIA, P; FONTANA, A; SPINELLI, D et al.Perkin transactions. 2. 1993, Num 4, pp 649-654, issn 0300-9580Article

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