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Citation: G. Bartoli et al., INTERNAL LEWIS-ACID COORDINATION AS A POWERFUL TOOL TO PROMOTE HIGHLYSTEREOSELECTIVE ALKYLATION OF ALPHA-ALKYL-BETA-HYDROXY KETONES WITH GRIGNARD-REAGENTS, Chemistry (Weinheim), 4(11), 1998, pp. 2154-2161
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Citation: R. Dalpozzo et al., SYNTHESIS OF BETA,GAMMA-UNSATURATED KETONES VIA CERIUM-MEDIATED ADDITION OF ORGANOLITHIUMS TO SILYLATED ENAMINONES, Journal of organic chemistry, 63(11), 1998, pp. 3745-3747
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Citation: G. Bartoli et al., OPPOSITE STEREOCHEMICAL EFFECTS EXERTED BY CECL3 AND TICL4 ON THE LEWIS ACID-MEDIATED REDUCTION OF ALPHA-ALKYL-BETA-KETOPHOSPHINE OXIDES WITH METALLIC HYDRIDES - A HIGHLY STEREOSELECTIVE PROTOCOL FOR THE SYNTHESIS OF SYN AND ANTI ALPHA-ALKYL-BETA-HYDROXYPHOSPHINE OXIDES, Chemistry, 3(12), 1997, pp. 1941-1950
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Citation: G. Bartoli et al., A STEREOSELECTIVE SYNTHESIS OF (E)-ALPHA,BETA-UNSATURATED KETONES INVOLVING THE REACTIONS OF ORGANOCERIUM REAGENTS WITH SECONDARY BETA-ENAMINO KETONES, Chemistry, 2(8), 1996, pp. 913-918
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Citation: G. Bartoli et al., ORGANO CERIUM REAGENTS IN ORGANIC-CHEMISTRY - GENERAL-METHOD OF SYNTHESIS OF ALKYL SUBSTITUTED 1,3-DIOLS BY RLI-CECL3 ADDITION TO BETA-HYDROXYKETONES, Tetrahedron letters, 37(13), 1996, pp. 2293-2296
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Citation: G. Bartoli et al., CERIUM CHLORIDE(III) PROMOTED NUCLEOPHILIC-ADDITION OF ORGANOLITHIUM REAGENTS TO ALPHA-DIPHENYLPHOSPHINOYL KETONES - AN EFFICIENT METHOD FOR THE SYNTHESIS OF HORNER-WITTIG INTERMEDIATES, Tetrahedron letters, 35(45), 1994, pp. 8453-8456
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Citation: G. Bartoli et al., HIGHLY STEREOSELECTIVE SYNTHESIS OF ALPHA,BETA-UNSATURATED KETONES BYCECL3 MEDIATED ADDITION OF GRIGNARD-REAGENTS TO BETA-ENAMINO KETONES, Journal of the Chemical Society, Chemical Communications, (6), 1994, pp. 715-716
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Citation: R. Ballini et al., REACTIVITY OF ALPHA-NITRO KETONES TOWARD ORGANOMETALLIC REAGENTS - STRAIGHTFORWARD SYNTHESIS OF TERTIARY BETA-NITROALKANOLS, Journal of organic chemistry, 58(12), 1993, pp. 3368-3372