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Titolo Data di pubblicazione Autore(i) File
1,3-Aminoalcohols by Reductive Cleavage of Isoxazolidines with Molybdenum Hexacarbonyl 1990 S. CICCHI; A. GOTI; A. BRANDI; A. GUARNA; F. DE SARLO
The Regioselectivity of Nitrone Cycloadditions to Vinyl Phosphorus Compounds 1990 A. BRANDI; S. CICCHI; A. GOTI; K.M. PIETRUSIEWICZ; W. WISNIEWSKI
Nitrone cycloaddition to 2,3-dihydro-1-phenyl-1h-phosphole 1-oxide. Double asymmetric induction and kinetic resolution by a chiral nitrone 1991 A. GOTI; S. CICCHI; A. BRANDI; K.M. PIETRUSIEWICZ
Direct Synthesis of Isoxazolidinylphosphines by Cycloaddition of Nitrones to Diphenylphosphinoethenes and X-Ray Structure of 7,7-Dimethyl-1-oxo-1-phenyl- 3-diphenylphosphinyl-hexahydropyrrolo[1,2-c]oxazaphosphorine 1991 K. M. PIETRUSIEWICZ; I. SALAMONCZYK; W. WIECZOREK; A. BRANDI; S. CICCHI; A. GOTI
Stereoselective Nitrone Additions to Vinyl Phosphine Derivatives: Effect of Phosphorus Substituents on Reaction Diastereoselectivity 1991 A. BRANDI; S. CICCHI; A. GOTI; K. M. PIETRUSIEWICZ; M. ZABLOCKA; W. WISNIEWSKI
Single and Double Asymmetric Induction in the Cycloaddition of Chiral Nitrones to Achiral and Chiral Vinylphosphine Oxides 1991 A. BRANDI; S. CICCHI; A. GOTI; K. M. PIETRUSIEWICZ
Regio- and Stereoselective Syntheses of Isoxazolidines Bearing Phosphinyl Substituents 1991 A. BRANDI; S. CICCHI; A. GOTI; K. M. PIETRUSIEWICZ
Radical Addition to Vinylphosphine Oxides: 1,2-Stereoinduction of Phosphorous Stereogenic Centre 1991 A. BRANDI; S. CICCHI; A. GOTI; K. M. PIETRUSIEWICZ
Crystal Structure and Stereochemistry of (PS*, 2S*, 3aS*)-Hexahydro-2- (tert-Butylvinylthiophosphinyl)-6,6-Dimethylpyrrolo[1,2-b]isoxazole 1991 K. M. PIETRUSIEWICZ; W. WIECZOREK; S. CICCHI; A. BRANDI
Chiral vinyl phosphine oxides: double asymmetric induction in the 1,3-dipolar cycloaddition to chiral nitrones. Kinetic resolution of a racemic phospholene oxide 1993 A. Brandi; S. Cicchi; A. Goti; K. M. Pietrusiewicz
New Synthesis of Five-Membered Cyclic Nitrones from Tartaric Acid 1993 S. Cicchi; I. Hold; A. Brandi
Synthesis of Lentiginosine by Stereoselective Chiral Nitrone Cycloaddition and Thermal Rearrangement of Strained Spiroisoxazolidine 1994 F. M. Cordero; S. Cicchi; A. Goti; A. Brandi
Assignment of the Absolute Configuration to Enantiomeric 2,3-Dihydro-1-phenyl-1H-phosphole 1-Sulfide. X-Ray Structure of (+)-(1S,3aR,7S,8S,8aR,8bR)-7,8-Di(tert-butoxy)-1-phenyloctahydro-1H-pyrrolo[1,2-b]-1H-phospholo[2,3-d]isoxazole1-sulfide 1994 K. M. Pietrusiewicz; W. Wieczoreck; S. Cicchi; A. Brandi
Kinetic Resolution in 1,3-Dipolar Cycloaddition of Tartaric Acid-Derived Nitrones to 2,3-Dihydro-1-phenyl-1H-phospholes. An Enantioselective Approach to the 2,2'-Coupled Pyrrolidine-Phospholane Ring System 1994 A. Brandi; S. Cicchi; A. Goti; M. Koprowski; K. M. Pietrusiewicz
Tertiary Phosphine Oxides: Preparations and Synthetic Applications 1995 S. CICCHI; A. BRANDI
A Five-membered Enantiopure Cyclic Nitrone from Malic Acid by Regioselective Oxidation of Cyclic Hydroxylamine. Synthesis of (1S,7S,8aR)-Octahydro-1,7-dihydroxyindolizine 1995 S. Cicchi; A. Goti; A. Brandi
Direct Chromatographic Resolution of P-Chiral Phosphinoylethenes on a Chiral Stationary Phase Containing N,N’-(3,5-Dinitrobenzoyl)-trans-1,2-diaminocyclohexane as Selector 1995 A. Brandi; S. Cicchi; F. Gasparrini; F. Maggio; C. Villani; M. Koprowski; K. M. Pietrusiewicz
A New P-Chiral Aminophosphine Ligand Containing a 2,2'-Coupled Pyrrolidine-Phospholane Ring System. Synthesis and Coordination Properties with Rodium(I) and Iridium(I) Fragments 1995 C. Bianchini; S. Cicchi; M. Peruzzini; K. M. Pietrusiewicz; A. Brandi
Assignment of the Absolute Configuration of Natural Lentiginosine by Synthesis and Enzymatic Assays of Optically Pure (+) and (–)-Enantiomers 1995 A. Brandi; S. Cicchi; F. M. Cordero; R. Frignoli; A. Goti; S. Picasso; P. Vogel
Synthesis and X-ray study of hexahydro- and tetrahydrophospholo[2,3-d]isoxazoles, a new class of heterocycles of potential fungicidal activity 1996 F. Machetti; B. Anichini; S. Cicchi; A. Brandi; W. Wieczoreck; K. M. Pietrusiewicz; J.-C. Gehret
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