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SYNTHESIS OF 1-AMINO-3-HYDROXY-ADAMANTANEDONETTI A; BELLORA E.1974; SYNTHET. COMMUNIC.; U.S.A.; DA. 1974; VOL. 3; NO 2; PP. 165-166; BIBL. 4 REF.Article

A MILD AND EFFECTIVE TWO-STEP CONVERSION OF DISUBSTITUTED CYANAMIDES TO SECONDARY AMINESDONETTI A; BELLORA E.1972; J. ORG. CHEM.; U.S.A.; DA. 1972; VOL. 37; NO 21; PP. 3352-3353; BIBL. 13 REF.Serial Issue

SYNTHESIS OF THE DIACETATE OF 4-CHLORO-2-HYDROXYMETHYL-2-BUTEN-1-OL: A USEFUL SYNTHON IN THE CHEMISTRY OF THE ISOPRENE UNITCEREDA E; BELLORA E; DONETTI A et al.1980; TETRAHEDRON LETT.; ISSN 0040-4039; GBR; DA. 1980; VOL. 21; NO 51; PP. 4977-4980; BIBL. 17 REF.Article

THE ACETATE OF (Z)-4-CHLORO-2-METHYL-2-BUTEN-1-OL. STEREOSELECTIVE WITTIG SYNTHESIS OF A NEW HEMITERPENOID SYNTHONCEREDA E; ATTOLINI M; BELLORA E et al.1982; TETRAHEDRON LETT.; ISSN 0040-4039; GBR; DA. 1982; VOL. 23; NO 21; PP. 2219-2222; BIBL. 12 REF.Article

SYNTHESIS AND ANALGETIC ACTIVITY OF N-SUBSTITUTED 6,7-BENZOMORPHANSBELLORA E; CEREDA E; EZHAYA A et al.1980; FARMACO, ED. SCI.; ITA; DA. 1980; VOL. 35; NO 6; PP. 490-497; ABS. ITA; BIBL. 18 REF.Article

A new, convenient synthesis of N2-aryl-N1-alkylformamidines and N2-aryl-N1,N1-dialkylformamidinesCEREDA, E; BELLORA, E; DONETTI, A et al.Synthesis (Stuttgart). 1986, Num 4, pp 288-291, issn 0039-7881Article

Synthesis of substituted N-arylpiperidines via organobismuth derivativesBANFI, A; BARTOLETTI, M; BELLORA, E et al.Synthesis (Stuttgart). 1994, Num 8, pp 775-776, issn 0039-7881Article

Anti-secretory and anti-ulcer activities of some new 2-(2-pyridylmethyl-sulfinyl)-benzimidazolesCEREDA, E; TURCONI, M; EZHAYA, A et al.European journal of medicinal chemistry. 1987, Vol 22, Num 6, pp 527-537, issn 0223-5234Article

New pyrrolidin-, piperidin- and azepin-2-oxocarboxylic acid esters are preferential M1, M3 muscarinic antagonists. Synthesis and bronchospasmolytic activityCEREDA, E; EZHAYA, A; BELLORA, E et al.European journal of medicinal chemistry. 1994, Vol 29, Num 6, pp 411-421, issn 0223-5234Article

(Imidazolylphenyl)formamidines: a structurally novel class of potent histamine H2 receptor antagonistsDONETTI, A; CEREDA, E; BELLORA, E et al.Journal of medicinal chemistry (Print). 1984, Vol 27, Num 3, pp 380-386, issn 0022-2623Article

Synthesis and biological evaluation of new antimuscarinic compounds with amidine basic centers. A useful bioisosteric replacement of classical cationic headsCEREDA, E; ZEHAYA, A; GIL QUINTERO, M et al.Journal of medicinal chemistry (Print). 1990, Vol 33, Num 8, pp 2108-2113, issn 0022-2623, 6 p.Article

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