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Titolo Data di pubblicazione Autore(i) File
A New Synthesis of (2S)-4-Oxopipecolic Acid by Thermal Rearrangement ofEnantiopure Spirocyclopropaneisoxazolidine 1996 F. Machetti; F. M. Cordero; F. De Sarlo; A. Guarna; A. Brandi
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
19-nor-10-azasteroids, a new class of steroid 5a-reductase inhibitors. 2. X-ray structure, molecular modeling, conformational analysis of 19-nor-10-azasteroids and comparison with 4-azasteroids and 6-azasteroids 1997 A. GUARNA; E. OCCHIATO; F. MACHETTI; G. DANZA; M. SERIO; P. PAOLI; A. MARRUCCI
Synthesis and Structure-Activity Relationship of 19-Nor-10-azasteroids, a New Class of 5α -Reductase Inhibitors in Human Prostate. 1997 A. GUARNA; Fabrizio MACHETTI; A. MARRUCCI; G. DANZA; M. SERIO.
New Synthesis of (Methoxycarbonyl)-indolizidine-7-one and -quinolizidine-2-one: an Access to β-Aminoacids with Indolizidine and Quinolizidine Backbone 1997 F. M. Cordero; F. Machetti; F. De Sarlo; A. Brandi
19-nor-10-azasteroids: a novel class of inhibitors for human steroid 5alpha-reductases 1 and 2 1997 A. GUARNA; C. BELLE; F. MACHETTI; E. OCCHIATO; A. H. PAYNE; C. CASSIANI; A; COMERCI; G. DANZA; A. DE BELLIS; S. DINI; A. MARRUCCI; M. SERIO
STEREOSELECTIVITY IN THE TICL4-CATALYSED REEACTION OF DANISHEFSKY¿S DIENE WITH A N-(ACYLOXY)IMINIUM ION: SYNTHESIS OF 5A VERSUS 5B D1(2)-19-NOR-10-AZASTEROIDS. PART 4 1998 E. OCCHIATO; D. SCARPI; F. MACHETTI; A. GUARNA
A CONCISE ROUTE TO 19-NOR-10-AZASTEROIDS, A NEW CLASS OF STEROID 5-REDUCTASE INHIBITORS. 3.1 SYNTHESIS OF (+)-19-NOR-10-AZATESTOSTERONE AND (+)-17B-ACETYLOXY-(5B)-10-AZAESTR-1-EN-3-ONE 1998 A. GUARNA; E. OCCHIATO; F. MACHETTI; D. SCARPI
19-NOR-10-AZASTEROIDS. 5.1 A SYNTHETIC STRATEGY FOR THE PREPARATION OF (+)-17-(3-PYRIDYL)-(5B)-10-AZAESTRA-1,16-DIEN-3-ONE, A NOVEL POTENTIAL INHIBITOR FOR HUMAN CYTOCHROME P45017A (17A-HYDROXYLASE/C17,20-LYASE) 1999 A. GUARNA; E. OCCHIATO; F. MACHETTI; V. GIACOMELLI
Synthesis and reactivity of bicycles derived from tartaric acids and alfa-amino acids: a novel class of conformationally constrained dipeptide isosteres based upon enantiopure 3-aza-6,8-dioxabicyclo[3.2.1]octane-7-carboxylic acid 1999 A. GUARNA; A. GUIDI; F. MACHETTI; G. MENCHI; E. OCCHIATO; D. SCARPI; S. SISI; A. TRABOCCHI
MODIFICATION OF THE AZA-ROBINSON ANNULATION FOR THE SYNTHESIS OF 4-METHYL-BENZO[C]QUINOLIZIN-3-ONES, POTENT INHIBITORS OF STEROID 5A-REDUCTASE 1 2000 A. GUARNA; F. MACHETTI; E. OCCHIATO; D. SCARPI; E. LOMBARDI
Oligomers of enantiopure bicyclic g/d-amino acids (BTAa). 1. Synthesis and conformational analysis of 3-Aza-6,8-dioxabicyclo[3.2.1]octane-7-carboxylic acid oligomers (PolyBTG) 2000 MACHETTI F.; FERRALI A.; MENCHI G.; OCCHIATO E.G.; A. GUARNA
BICYCLIC DIPEPTIDE ISOSTERES, THEIR PREPARATION AND USE AS BETA-TURN MIMICS 2000 F. M. CORDERO; A. BRANDI; S. VALENZA; F. MACHETTI
Emerging drugs for the third millenium. Discovery and development of the inhibitors of steroids 5alpha-reductase as drugs for the androgen-dependant diaseas 2000 A.Guarna; E.G.Occhiato; F.Machetti; G.Danza; M.Serio
3-Aza-6,8-dioxabicyclo (3,2,1) octanes and analogues and combinatorial libraries 2000 GUARNA A; E. OCCHIATO; SCARPI D; MENCHI G; MACHETTI F
Benzo[c]quinolizin-3-ones: a novel class of potent and selective nonsteroidal inhibitors of human steroid 5alpha-reductase 1 2000 A. GUARNA; F. MACHETTI; E. OCCHIATO; D. SCARPI; A. COMERCI; G. DANZA; R. MANCINA; M. SERIO; K. HARDY
Synthesis of Taurine Analogues from Alkenes 2000 F. MACHETTI; M. CACCIARINI; F. CATRAMBONE; F. M. CORDERO; M. FROSINI; F. DE SARLO
SYNTHESIS OF TAURINE ANALOGUES. PART 1: 2-AMINOSULFONIC ACIDS FROM ALKENE-SULFUR MONOCHLORIDE ADDUCTS 2000 F. MACHETTI; M. CACCIARINI; F. CATRAMBONE; F. M. CORDERO; S. ROMOLI; F. DE SARLO;
Practical synthesis of both enantiomers of protected 4-oxopipecolic acid. 2001 F. MACHETTI; F. M. CORDERO; F. DE SARLO; A. BRANDI
Effect of C-Ring Modifications in Benzo[c]quinolizin-3-ones, New Selective Inhibitors of Human 5a-Reductase 1 2001 A. GUARNA; E.G. OCCHIATO; F. MACHETTI; A. TRABOCCHI; D. SCARPI; G. DANZA; R. MANCINA; A. COMERCI; M. SERIO
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