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Încăpăţânat Descriptiv Oraș andrea trabocchi nicoletta cini gloria menchi and antonio guarna La bord Taxa de admitere victorie

Antonio GUARNA | Professor (Full) | Full Professor in Organic Chemistry |  University of Florence, Florence | UNIFI | Dipartimento di Chimica "Ugo  Schiff" - Page 2
Antonio GUARNA | Professor (Full) | Full Professor in Organic Chemistry | University of Florence, Florence | UNIFI | Dipartimento di Chimica "Ugo Schiff" - Page 2

Menchi GLORIA | University of Florence, Florence | UNIFI | Dipartimento di  Chimica "Ugo Schiff"
Menchi GLORIA | University of Florence, Florence | UNIFI | Dipartimento di Chimica "Ugo Schiff"

Title of the abstract, centered, in bold face, using 14 pt Times New ...
Title of the abstract, centered, in bold face, using 14 pt Times New ...

Andrea TRABOCCHI | Associate Professor | University of Florence, Florence |  UNIFI | Dipartimento di Chimica "Ugo Schiff" - Page 2
Andrea TRABOCCHI | Associate Professor | University of Florence, Florence | UNIFI | Dipartimento di Chimica "Ugo Schiff" - Page 2

Antonio GUARNA | Professor (Full) | Full Professor in Organic Chemistry |  University of Florence, Florence | UNIFI | Dipartimento di Chimica "Ugo  Schiff"
Antonio GUARNA | Professor (Full) | Full Professor in Organic Chemistry | University of Florence, Florence | UNIFI | Dipartimento di Chimica "Ugo Schiff"

Anna BOTTONCETTI | biological science | University of Florence, Florence |  UNIFI | medicina nucleare biomolecolare
Anna BOTTONCETTI | biological science | University of Florence, Florence | UNIFI | medicina nucleare biomolecolare

Menchi GLORIA | University of Florence, Florence | UNIFI | Dipartimento di  Chimica "Ugo Schiff"
Menchi GLORIA | University of Florence, Florence | UNIFI | Dipartimento di Chimica "Ugo Schiff"

Influence of Chirality of the Preceding Acyl Moiety on the cis/trans Ratio  of the Proline Peptide Bond | The Journal of Organic Chemistry
Influence of Chirality of the Preceding Acyl Moiety on the cis/trans Ratio of the Proline Peptide Bond | The Journal of Organic Chemistry

Bioorganic & Medicinal Chemistry | Vol 14, Issue 15, Pages 5073-5428 (1  August 2006) | ScienceDirect.com by Elsevier
Bioorganic & Medicinal Chemistry | Vol 14, Issue 15, Pages 5073-5428 (1 August 2006) | ScienceDirect.com by Elsevier

Stereoisomerism and Biological Activity of the Selective and Superactive  αvβ3 Integrin Inhibitor cyclo(-RGDfV-) and Its Retro-Inverso Peptide |  Journal of the American Chemical Society
Stereoisomerism and Biological Activity of the Selective and Superactive αvβ3 Integrin Inhibitor cyclo(-RGDfV-) and Its Retro-Inverso Peptide | Journal of the American Chemical Society

Menchi GLORIA | University of Florence, Florence | UNIFI | Dipartimento di  Chimica "Ugo Schiff"
Menchi GLORIA | University of Florence, Florence | UNIFI | Dipartimento di Chimica "Ugo Schiff"

Synthesis and Reactivity of Bicycles Derived from Tartaric Acid and α-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 | The Journal of Organic ...
Synthesis and Reactivity of Bicycles Derived from Tartaric Acid and α-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 | The Journal of Organic ...

Menchi GLORIA | University of Florence, Florence | UNIFI | Dipartimento di  Chimica "Ugo Schiff"
Menchi GLORIA | University of Florence, Florence | UNIFI | Dipartimento di Chimica "Ugo Schiff"

3-Aza-6,8-dioxabicyclo[3.2.1]octanes as new enantiopure heteroatom-rich  tropane-like ligands of human dopamine transporter - ScienceDirect
3-Aza-6,8-dioxabicyclo[3.2.1]octanes as new enantiopure heteroatom-rich tropane-like ligands of human dopamine transporter - ScienceDirect

PDF) Synthesis of a bicyclic δ-amino acid as a constrained Gly-Asn  dipeptide isostere
PDF) Synthesis of a bicyclic δ-amino acid as a constrained Gly-Asn dipeptide isostere

WO2011098603A1 - 1,2,3-triazole-based peptidomimetic integrin inhibitors  for the diagnosis and therapy of tumors - Google Patents
WO2011098603A1 - 1,2,3-triazole-based peptidomimetic integrin inhibitors for the diagnosis and therapy of tumors - Google Patents

Menchi GLORIA | University of Florence, Florence | UNIFI | Dipartimento di  Chimica "Ugo Schiff"
Menchi GLORIA | University of Florence, Florence | UNIFI | Dipartimento di Chimica "Ugo Schiff"

Menchi GLORIA | University of Florence, Florence | UNIFI | Dipartimento di  Chimica "Ugo Schiff"
Menchi GLORIA | University of Florence, Florence | UNIFI | Dipartimento di Chimica "Ugo Schiff"

2-Carbomethoxy-3-aryl-8-bicyclo[3.2.1]octanes: Potent Non-Nitrogen  Inhibitors of Monoamine Transporters | Journal of Medicinal Chemistry
2-Carbomethoxy-3-aryl-8-bicyclo[3.2.1]octanes: Potent Non-Nitrogen Inhibitors of Monoamine Transporters | Journal of Medicinal Chemistry

Menchi GLORIA | University of Florence, Florence | UNIFI | Dipartimento di  Chimica "Ugo Schiff"
Menchi GLORIA | University of Florence, Florence | UNIFI | Dipartimento di Chimica "Ugo Schiff"

Antonio GUARNA | Professor (Full) | Full Professor in Organic Chemistry |  University of Florence, Florence | UNIFI | Dipartimento di Chimica "Ugo  Schiff"
Antonio GUARNA | Professor (Full) | Full Professor in Organic Chemistry | University of Florence, Florence | UNIFI | Dipartimento di Chimica "Ugo Schiff"

Antonio GUARNA | Professor (Full) | Full Professor in Organic Chemistry |  University of Florence, Florence | UNIFI | Dipartimento di Chimica "Ugo  Schiff" - Page 2
Antonio GUARNA | Professor (Full) | Full Professor in Organic Chemistry | University of Florence, Florence | UNIFI | Dipartimento di Chimica "Ugo Schiff" - Page 2

Discovery of a Potent, Selective Protein Tyrosine Phosphatase 1B Inhibitor  Using a Linked-Fragment Strategy | Journal of the American Chemical Society
Discovery of a Potent, Selective Protein Tyrosine Phosphatase 1B Inhibitor Using a Linked-Fragment Strategy | Journal of the American Chemical Society

Design, synthesis, and conformational analysis of a novel spiro-bicyclic  system as a type II .beta.-turn peptidomimetic | Journal of the American  Chemical Society
Design, synthesis, and conformational analysis of a novel spiro-bicyclic system as a type II .beta.-turn peptidomimetic | Journal of the American Chemical Society